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Wyszukujesz frazę ""Chromosomes, Human, Pair 1"" wg kryterium: Temat


Tytuł:
Chromosomal region 1q24.1 is associated with increased risk of schizophrenia in Pakistani population.
Autorzy:
Fatima W; Department of Microbiology and Molecular Genetics, University of the Punjab, Lahore, Pakistan. Electronic address: .
Riaz S; Department of Microbiology and Molecular Genetics, University of the Punjab, Lahore, Pakistan.
Aiman Shahzad M; Department of Allied Health Sciences, University of Health Sciences, Lahore, Pakistan.
Naz Z; Department of Microbiology and Molecular Genetics, University of the Punjab, Lahore, Pakistan.
Mahmood S; Department of Allied Health Sciences, University of Health Sciences, Lahore, Pakistan.
Hasnain S; Department of Microbiology and Molecular Genetics, University of the Punjab, Lahore, Pakistan.
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Źródło:
Gene [Gene] 2020 Apr 15; Vol. 734, pp. 144390. Date of Electronic Publication: 2020 Jan 24.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Schizophrenia/*genetics
Adult ; Female ; Genetic Markers ; Genetic Predisposition to Disease ; Genotype ; Haplotypes ; Humans ; Linkage Disequilibrium ; Male ; Pakistan
Czasopismo naukowe
Tytuł:
Co-polysomy of 1p/19q in glial tumors: Retrospective analysis of 221 cases from single center.
Autorzy:
Kuskucu A; Department of Medical Genetics, Yeditepe University Medical School, 34755 Istanbul, Turkey.
Tuysuz EC; Department of Medical Genetics, Yeditepe University Medical School, 34755 Istanbul, Turkey; Department of Biotechnology, Institute of Science, Yeditepe University, 34755 Istanbul, Turkey.
Gurkan S; Department of Medical Genetics, Yeditepe University Medical School, 34755 Istanbul, Turkey.
Demir Z; Department of Medical Genetics, Yeditepe University Medical School, 34755 Istanbul, Turkey.
Yaltirik CK; Department of Neurosurgery, Yeditepe University Medical School, Yeditepe University, 34755 Istanbul, Turkey.
Ozkan F; Department of Medical Pathology, Yeditepe University Medical School, Yeditepe University, 34755 Istanbul, Turkey.
Ekici ID; Department of Medical Pathology, Yeditepe University Medical School, Yeditepe University, 34755 Istanbul, Turkey.
Bayrak OF; Department of Medical Genetics, Yeditepe University Medical School, 34755 Istanbul, Turkey. Electronic address: .
Ture U; Department of Neurosurgery, Yeditepe University Medical School, Yeditepe University, 34755 Istanbul, Turkey. Electronic address: .
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Źródło:
Gene [Gene] 2019 Jun 15; Vol. 701, pp. 161-168. Date of Electronic Publication: 2019 Mar 05.
Typ publikacji:
Clinical Trial; Journal Article
MeSH Terms:
Biomarkers, Tumor*/biosynthesis
Biomarkers, Tumor*/genetics
Brain Neoplasms*/genetics
Brain Neoplasms*/metabolism
Brain Neoplasms*/mortality
Brain Neoplasms*/pathology
Chromosome Aberrations*
Chromosomes, Human, Pair 1*/genetics
Chromosomes, Human, Pair 1*/metabolism
Gene Expression Regulation, Neoplastic*
Neoplasm Proteins*/biosynthesis
Neoplasm Proteins*/genetics
Oligodendroglioma*/genetics
Oligodendroglioma*/metabolism
Oligodendroglioma*/mortality
Oligodendroglioma*/pathology
Adult ; Disease-Free Survival ; Female ; Follow-Up Studies ; Humans ; Male ; Middle Aged ; Retrospective Studies ; Survival Rate
Czasopismo naukowe
Tytuł:
Acute myeloid leukemia associated with t(1;3)(p36;q21) and extreme thrombocytosis: a clinical study with literature review.
Autorzy:
Lim G; Department of Laboratory Medicine, School of Medicine, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul 130-702, Korea.
Kim MJ
Oh SH
Cho SY
Lee HJ
Suh JT
Lee J
Lee WI
Cho KS
Park TS
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2010 Dec; Vol. 203 (2), pp. 187-92.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 3*
Translocation, Genetic*
Leukemia, Myeloid, Acute/*genetics
Thrombocytosis/*genetics
Adult ; Aged ; Bone Marrow Cells/cytology ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
A case of angioimmunoblastic T-cell non-Hodgkin lymphoma with a neocentric inv dup(1).
Autorzy:
Blom E; Department of Clinical Genetics, Leiden University Medical Center, The Netherlands.
Heyning FH
Kroes WG
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2010 Oct 01; Vol. 202 (1), pp. 38-42.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosome Inversion*
Chromosomes, Human, Pair 1*
Gene Duplication*
Antineoplastic Combined Chemotherapy Protocols/*therapeutic use
Immunoblastic Lymphadenopathy/*genetics
Lymphoma, T-Cell/*genetics
Aged ; Antineoplastic Combined Chemotherapy Protocols/administration & dosage ; Cyclophosphamide/administration & dosage ; Doxorubicin/administration & dosage ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Lymphoma, B-Cell/drug therapy ; Lymphoma, B-Cell/pathology ; Lymphoma, T-Cell/drug therapy ; Male ; Neoplasms, Second Primary ; Prednisone/administration & dosage ; Vincristine/administration & dosage
SCR Protocol:
CHOP protocol
Czasopismo naukowe
Tytuł:
A novel case of t(X;1)(p11.2;p34) in a renal cell carcinoma with TFE3 rearrangement and favorable outcome in a 57-year-old patient.
Autorzy:
Haudebourg J; Department of Pathology, Nice University Hospital, 33 Avenue Valombrose, Nice Cedex 1, France. />Hoch B
Fabas T
Burel-Vandenbos F
Carpentier X
Amiel J
Cardot-Leccia N
Michiels JF
Pedeutour F
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2010 Jul 15; Vol. 200 (2), pp. 75-8.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, X*
Gene Rearrangement*
Translocation, Genetic*
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors/*genetics
Carcinoma, Renal Cell/*genetics
Kidney Neoplasms/*genetics
Carcinoma, Renal Cell/pathology ; Female ; Humans ; Kidney Neoplasms/pathology ; Middle Aged
Czasopismo naukowe
Tytuł:
Heterozygosity status of 1p and 19q and its correlation with p53 protein expression and EGFR amplification in patients with astrocytic tumors: novel series from India.
Autorzy:
Jha P; Department of Pathology, All India Institute of Medical Sciences (AIIMS), New Delhi 110029, India.
Agarwal S
Pathak P
Srivastava A
Suri V
Sharma MC
Chosdol K
Srivastava T
Gupta D
Gupta A
Suri A
Sarkar C
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2010 Apr 15; Vol. 198 (2), pp. 126-34.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Gene Amplification*/physiology
Genes, erbB-1*
Astrocytoma/*genetics
Brain Neoplasms/*genetics
Tumor Suppressor Protein p53/*genetics
Adolescent ; Adult ; Aged ; Astrocytoma/metabolism ; Astrocytoma/pathology ; Brain Neoplasms/metabolism ; Brain Neoplasms/pathology ; Case-Control Studies ; Child ; Female ; Heterozygote ; Humans ; India ; Loss of Heterozygosity ; Male ; Middle Aged ; Tumor Suppressor Protein p53/metabolism ; Young Adult
Czasopismo naukowe
Tytuł:
Genomic deletions at 1p and 14q are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not in schwannomas.
Autorzy:
Martínez-Glez V; Research Unit-Unidad de Investigación, Hospital Universiatrio La Paz, Paseo Castellana 261, 28046 Madrid, Spain.
Alvarez L
Franco-Hernández C
Torres-Martin M
de Campos JM
Isla A
Vaquero J
Lassaletta L
Castresana JS
Casartelli C
Rey JA
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2010 Jan 01; Vol. 196 (1), pp. 1-6.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 14*
Gene Expression Profiling*
Genomics*
Oligonucleotide Array Sequence Analysis*
Meningioma/*genetics
Neurilemmoma/*genetics
DNA, Complementary/genetics ; Humans
Czasopismo naukowe
Tytuł:
Derivative (1)t(1;16)(p11;p11.1) in myelodysplastic syndrome: a case report and review of the literature.
Autorzy:
Lunghi M; Division of Hematology, Amedeo Avogadro University of Eastern Piedmont and Ospedale Maggiore della Carità, Via Solaroli 17, 28100 Novara, Italy. />Casorzo L
De Paoli L
Riccomagno P
Rossi D
Gaidano G
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2010 Jan 01; Vol. 196 (1), pp. 89-92.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 16*
Translocation, Genetic*
Myelodysplastic Syndromes/*genetics
Aged, 80 and over ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male
Czasopismo naukowe
Tytuł:
A novel t(1;2)(p33;q33) in secondary postpolycythemic myelofibrosis.
Autorzy:
Panani AD
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Dec; Vol. 195 (2), pp. 201-2.
Typ publikacji:
Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 2*
Translocation, Genetic*
Polycythemia/*genetics
Primary Myelofibrosis/*genetics
Humans ; Karyotyping ; Polycythemia/complications ; Primary Myelofibrosis/complications
Opinia redakcyjna
Tytuł:
Does MDS with der(1;7)(q10;p10) constitute a distinct risk group? A retrospective single institutional analysis of clinical/pathologic features compared to -7/del(7q) MDS.
Autorzy:
Slovak ML; Cytogenetics Laboratory, City of Hope, 1500 E. Duarte Road, Duarte, CA 91010, USA. />O'Donnell M
Smith DD
Gaal K
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Sep; Vol. 193 (2), pp. 78-85.
Typ publikacji:
Comparative Study; Journal Article
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Genetic Predisposition to Disease*
Myelodysplastic Syndromes/*genetics
Adult ; Aged ; Aged, 80 and over ; Female ; Humans ; Male ; Middle Aged ; Prognosis ; Retrospective Studies
Czasopismo naukowe
Tytuł:
Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant.
Autorzy:
Tirado CA
Chen W
Valdez FJ
Henderson S
Doolittle J
Garcia R
Patel S
Holdridge S
Chastain C
Collins RH
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Aug; Vol. 193 (1), pp. 67-9.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 21*
Chromosomes, Human, Pair 8*
Core Binding Factor Alpha 2 Subunit/*genetics
Leukemia, Myeloid, Acute/*genetics
Humans ; In Situ Hybridization, Fluorescence ; Male ; Middle Aged ; Translocation, Genetic
Raport
Tytuł:
t(1;16)(q10;p10) as the sole karyotypic abnormality in acute myeloid leukemia.
Autorzy:
Takahashi T
Suzuki M
Tsukuda H
Kimura H
Yoshimoto M
Tsujisaki M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Jul; Vol. 192 (1), pp. 52-3.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 16*
Translocation, Genetic*
Leukemia, Myeloid, Acute/*genetics
Aged ; Chromosome Aberrations ; Female ; Humans
Raport
Tytuł:
Derivative (1)t(1;19)(p13;p13) in the setting of myelofibrosis with JAK2 V617F.
Autorzy:
Staropoli JF
Wadleigh M
Dal Cin P
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Jun; Vol. 191 (2), pp. 109-10.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Translocation, Genetic*
Janus Kinase 2/*genetics
Primary Myelofibrosis/*genetics
Thrombocytosis/*genetics
Adult ; Amino Acid Substitution ; Bone Marrow/pathology ; Chromosome Mapping ; Female ; Humans ; Karyotyping ; Metaphase/genetics ; Primary Myelofibrosis/pathology ; Thrombocytosis/pathology ; Trisomy/genetics
Raport
Tytuł:
Two case reports of 1q triplication in myeloproliferative neoplasms.
Autorzy:
Park TS
Lee SG
Cheong JW
Song J
Lee KA
Kim J
Yoon S
Choi JR
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Jun; Vol. 191 (2), pp. 111-2.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Mutagenesis*
Leukemia, Myelogenous, Chronic, BCR-ABL Positive/*genetics
Myeloproliferative Disorders/*genetics
Adult ; Female ; Humans ; Karyotyping ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/pathology ; Male ; Metaphase ; Middle Aged ; Myeloproliferative Disorders/pathology
Raport
Tytuł:
A tandem triplication, trp(1)(q21q32), in a patient with follicular lymphoma: a case study and review of the literature.
Autorzy:
Park TS; Department of Laboratory Medicine, Yonsei University College of Medicine, 250 Seongsanno, Seodaemun-gu, Seoul, 120-752, Korea.
Lee ST
Song J
Lee KA
Kim J
Kim SJ
Lee JH
Song S
Choi JR
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Mar; Vol. 189 (2), pp. 127-31.
Typ publikacji:
Case Reports; Journal Article; Review
MeSH Terms:
Chromosomes, Human, Pair 1*
Tandem Repeat Sequences*
Lymphoma, Follicular/*genetics
Aged ; Cytogenetic Analysis ; Gene Duplication ; Humans ; Male ; Trisomy
Czasopismo naukowe
Tytuł:
Inverted duplication dup(1)(q32q21) as sole aberration in lymphoid and myeloid malignancies.
Autorzy:
Bacher U; Interdisciplinary Clinic for Stem Cell Transplantation, University Cancer Center Hamburg, Germany.
Schnittger S
Grüneisen A
Haferlach T
Kern W
Haferlach C
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Jan 15; Vol. 188 (2), pp. 108-11.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosome Aberrations*
Chromosome Inversion*
Chromosomes, Human, Pair 1*
Myelodysplastic Syndromes/*genetics
Myeloproliferative Disorders/*genetics
Adult ; Aged ; Chromosome Banding ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Middle Aged ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics ; Trisomy
Czasopismo naukowe
Tytuł:
Pattern of trisomy 1q in hematological malignancies: a single institution experience.
Autorzy:
Djordjević V; Institute of Hematology, Clinical Center of Serbia, 2 Koste Todorovicaa, Belgrade, Serbia. />Dencić-Fekete M
Jovanović J
Drakulić D
Stevanović M
Janković G
Gotić M
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2008 Oct; Vol. 186 (1), pp. 12-8.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Trisomy*
Hematologic Neoplasms/*genetics
Adult ; Aged ; Chromosome Painting ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Leukemia, Myeloid, Acute/genetics ; Male ; Middle Aged ; Myelodysplastic Syndromes/genetics ; Myeloproliferative Disorders/genetics ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics ; Translocation, Genetic
Czasopismo naukowe
Tytuł:
Assessment of 1p/19q deletions by fluorescence in situ hybridization in gliomas.
Autorzy:
Reddy KS; Genzyme Genetics, 521 West 57th Street, New York, NY 10025, USA.
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2008 Jul 15; Vol. 184 (2), pp. 77-86.
Typ publikacji:
Evaluation Study; Journal Article
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Brain Neoplasms/*genetics
Glioma/*genetics
In Situ Hybridization, Fluorescence/*methods
Adult ; Aged ; Biomarkers, Tumor/genetics ; Brain Neoplasms/diagnosis ; Cohort Studies ; Female ; Glioma/diagnosis ; Humans ; Male ; Middle Aged ; Prognosis
Czasopismo naukowe
Tytuł:
Imatinib resistance in a novel translocation der(17)t(1;17)(q25;p13) with loss of TP53 but without BCR/ABL kinase domain mutation in chronic myelogenous leukemia.
Autorzy:
Yamamoto K; Hematology/Oncology, Department of Medicine, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan.
Yakushijin K
Nishikawa S
Minagawa K
Katayama Y
Shimoyama M
Matsui T
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2008 May; Vol. 183 (1), pp. 77-81.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 17*
Genes, p53*
Translocation, Genetic*
Leukemia, Myelogenous, Chronic, BCR-ABL Positive/*drug therapy
Leukemia, Myelogenous, Chronic, BCR-ABL Positive/*genetics
Piperazines/*therapeutic use
Protein-Tyrosine Kinases/*genetics
Pyrimidines/*therapeutic use
Adult ; Benzamides ; Disease Progression ; Drug Resistance, Neoplasm/genetics ; Fusion Proteins, bcr-abl ; Gene Deletion ; Genes, abl ; Humans ; Imatinib Mesylate ; Male ; Mutation ; Protein Structure, Tertiary/genetics ; Protein-Tyrosine Kinases/chemistry
Czasopismo naukowe
Tytuł:
Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo.
Autorzy:
Macedo Silva ML; National Center for Bone Marrow Transplant, National Cancer Institute, Rio de Janeiro, Brazil. />Raimondi SC
Abdelhay E
Gross M
Mkrtchyan H
de Figueiredo AF
Ribeiro RC
de Jesus Marques-Salles T
Sobral ES
Gerardin Land MP
Liehr T
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2008 Apr 01; Vol. 182 (1), pp. 56-60.
Typ publikacji:
Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 16*
Oncogene Proteins, Fusion*
Translocation, Genetic*
Leukemia, Myelomonocytic, Acute/*genetics
Chromosome Banding ; Humans ; In Situ Hybridization, Fluorescence ; Infant ; Karyotyping ; Male
Czasopismo naukowe
Tytuł:
Molecular cytogenetic findings in a three-way novel variant of t(1;8;21)(p35;q22;q22): a unique relocation of the AML1/ETO fusion gene 1p35 in AML-M2.
Autorzy:
Ahmad F; Research and Development, SRL Ranbaxy Ltd., MIDC, Andheri (E), Mumbai-400093, India.
Kokate P
Chheda P
Dalvi R
Das BR
Mandava S
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2008 Jan 15; Vol. 180 (2), pp. 153-7.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 21*
Chromosomes, Human, Pair 8*
Translocation, Genetic*
Core Binding Factor Alpha 2 Subunit/*genetics
Leukemia, Myeloid, Acute/*genetics
Oncogene Proteins, Fusion/*genetics
Base Sequence ; Chromosome Mapping ; Cytogenetic Analysis ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Middle Aged ; RUNX1 Translocation Partner 1 Protein
Czasopismo naukowe
Tytuł:
CREB3L4, INTS3, and SNAPAP are targets for the 1q21 amplicon frequently detected in hepatocellular carcinoma.
Autorzy:
Inagaki Y; Molecular Gastroenterology and Hepatology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, 465 Kajii-cho Kamigyo-ku, Kyoto 602-8566, Japan.
Yasui K
Endo M
Nakajima T
Zen K
Tsuji K
Minami M
Tanaka S
Taniwaki M
Itoh Y
Arii S
Okanoue T
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2008 Jan 01; Vol. 180 (1), pp. 30-6.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Gene Amplification*
Proto-Oncogenes*
Basic-Leucine Zipper Transcription Factors/*genetics
Carcinoma, Hepatocellular/*genetics
Liver Neoplasms/*genetics
Nuclear Proteins/*genetics
Vesicular Transport Proteins/*genetics
Chromosome Mapping ; Cyclic AMP Response Element-Binding Protein ; Gene Dosage ; Humans ; In Situ Hybridization, Fluorescence ; Oligonucleotide Array Sequence Analysis ; Polymerase Chain Reaction ; Polymorphism, Single Nucleotide ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł:
A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia.
Autorzy:
Park TS; Department of Laboratory Medicine, Yonsei University College of Medicine, 250 Seongsanno, Seodaemun-gu, Seoul 120-752, Korea.
Song J
Lee KA
Lee SG
Yoon S
Kim JS
Lyu CJ
Choi JR
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Dec; Vol. 179 (2), pp. 132-5.
Typ publikacji:
Case Reports; Journal Article; Review
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 15*
Translocation, Genetic*
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Child ; Humans ; Karyotyping ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Rare t(1;11)(q23;p15) in therapy-related myelodysplastic syndrome evolving into acute myelomonocytic leukemia: a case report and review of the literature.
Autorzy:
Zhang L; Department of Pathology and Laboratory, Cedars Sinai Medical Center, 8700 Beverly Boulevard, Room 4711, Los Angeles, CA 90048, USA. />Alsabeh R
Mecucci C
La Starza R
Gorello P
Lee S
Lill M
Schreck R
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Oct 01; Vol. 178 (1), pp. 42-8.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 11*
Translocation, Genetic*
Leukemia, Myelomonocytic, Acute/*genetics
Myelodysplastic Syndromes/*genetics
Myelodysplastic Syndromes/*pathology
Myelodysplastic Syndromes/*therapy
Adult ; Aged ; Disease Progression ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Middle Aged ; Neutrophils/metabolism
Czasopismo naukowe
Tytuł:
Molecular cytogenetic analysis of complex karyotypes with derivative chromosome der(1)t(1;5) found in two patients with myeloid leukemia.
Autorzy:
Melichercíková J; Institute of Hematology and Blood Transfusion, U Nemocnice 1, 128 20 Prague 2, Czech Republic.
Brezinová J
Zemanová Z
Cermák J
Michalová K
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Jul 15; Vol. 176 (2), pp. 150-5.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 5*
Translocation, Genetic*
Leukemia, Myeloid/*genetics
Adult ; Cytogenetic Analysis ; Humans ; Karyotyping ; Male ; Middle Aged ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł:
Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia.
Autorzy:
Crescenzi B; Department of Hematology, University of Perugia, IBiT Foundation (Fondazione IRCCS Biotecnologie nel Trapianto), via Brunamonti 51, 06122 Perugia, Italy.
La Starza R
Nozzoli C
Ciolli S
Matteucci C
Romoli S
Rigacci L
Gorello P
Bosi A
Martelli MF
Marynen P
Mecucci C
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Jul 01; Vol. 176 (1), pp. 67-71.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 12*
Chromosomes, Human, Pair 5*
Translocation, Genetic*
Leukemia, Myelomonocytic, Chronic/*genetics
Oncogene Proteins, Fusion/*genetics
Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Endometrioid-like yolk sac and Sertoli-Leydig cell tumors in a carrier of a Y heterochromatin insertion into 1qh region: a causal association?
Autorzy:
Sala E; Genetic Laboratory, H.S. Gerardo, Monza, Italy.
Villa N
Crosti F
Miozzo M
Perego P
Cappellini A
Bonazzi C
Barisani D
Dalprà L
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Mar; Vol. 173 (2), pp. 164-9.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Y*
Endodermal Sinus Tumor/*pathology
Ovarian Neoplasms/*pathology
Sertoli-Leydig Cell Tumor/*pathology
Translocation, Genetic/*genetics
Carcinoma, Endometrioid/pathology ; Chromosome Mapping/methods ; Endodermal Sinus Tumor/genetics ; Female ; Heterochromatin/genetics ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Loss of Heterozygosity ; Ovarian Neoplasms/genetics ; Sequence Tagged Sites ; Sertoli-Leydig Cell Tumor/genetics
Czasopismo naukowe
Tytuł:
A rare case of acute myeloid leukemia evolving from a myelodysplastic syndrome with der(19)t(1;19).
Autorzy:
Pinheiro RF
Chauffaille Mde L
Silva MR
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2006 Sep; Vol. 169 (2), pp. 181-3.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Translocation, Genetic*
Leukemia, Myeloid/*genetics
Myelodysplastic Syndromes/*complications
Acute Disease ; Adult ; Aged ; Female ; Humans ; Leukemia, Myeloid/etiology
Raport
Tytuł:
Secondary acute myeloid leukemia with a t(1;11)(q23;p15) in an adolescent treated for testicular sarcoma.
Autorzy:
Soares EM
Santos N
de Araújo Silva Amaral B
Silva ML
Leite EP
Silva MO
Muniz MT
Ribeiro RC
de Morais VL
de Jesus Marques Salles T
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2006 Aug; Vol. 169 (1), pp. 83-5.
Typ publikacji:
Case Reports; Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 11*
Antineoplastic Combined Chemotherapy Protocols/*adverse effects
Leukemia, Myeloid/*genetics
Sarcoma/*genetics
Testicular Neoplasms/*drug therapy
Testicular Neoplasms/*genetics
Acute Disease ; Adolescent ; Humans ; Karyotyping ; Leukemia, Myeloid/chemically induced ; Male
Raport
Tytuł:
Trisomy 1q in a patient with severe aplastic anemia.
Autorzy:
Angelidis P; Department of Medicine, University of Oklahoma Health Sciences Center, 941 Stanton L. Young Blvd, Oklahoma City, OK 73104, USA.
Kojouri K
Lee J
Kern W
Mulvihill JJ
Li S
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2006 Aug; Vol. 169 (1), pp. 73-5.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Trisomy*
Anemia, Aplastic/*genetics
Adult ; Female ; Humans ; Karyotyping
Czasopismo naukowe
Tytuł:
Isochromosome 1q in a myelodysplastic syndrome after treatment for acute promyelocytic leukemia.
Autorzy:
Pawarode A; Leukemia Section, Department of Medicine, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USA.
Finlay E
Sait SN
Barcos M
Baer MR
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2006 Jun; Vol. 167 (2), pp. 155-60.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*/ultrastructure
Isochromosomes*
Antineoplastic Agents/*adverse effects
Cytarabine/*adverse effects
Daunorubicin/*adverse effects
Leukemia, Promyelocytic, Acute/*drug therapy
Myelodysplastic Syndromes/*genetics
Adult ; Female ; Humans ; Leukemia, Promyelocytic, Acute/pathology ; Male ; Middle Aged ; Myelodysplastic Syndromes/chemically induced ; Myelodysplastic Syndromes/diagnosis
Czasopismo naukowe
Tytuł:
Derivative (1;7)(q10;p10) in multiple myeloma. A sign of therapy-related hidden myelodysplastic syndrome.
Autorzy:
Ishii Y; The First Department of Internal Medicine, Tokyo Medical University, 6-7-1 Nishi-shinjuku, Tokyo 160-0023, Japan.
Hsiao HH
Sashida G
Ito Y
Miyazawa K
Kodama A
Ohyashiki JH
Ohyashiki K
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2006 Jun; Vol. 167 (2), pp. 131-7.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Antineoplastic Agents, Alkylating/*adverse effects
Melphalan/*adverse effects
Multiple Myeloma/*drug therapy
Myelodysplastic Syndromes/*genetics
Aged ; Aged, 80 and over ; Female ; Humans ; Male ; Middle Aged ; Multiple Myeloma/complications ; Multiple Myeloma/diagnosis ; Myelodysplastic Syndromes/diagnosis ; Myelodysplastic Syndromes/epidemiology
Czasopismo naukowe
Tytuł:
Additional cytogenetic changes and previous genotoxic exposure predict unfavorable prognosis in myelodysplastic syndromes and acute myeloid leukemia with der(1;7)(q10;p10).
Autorzy:
Hsiao HH; The First Department of Internal Medicine; Department of Internal Medicine, Kaohsiung Medical University Hospital, 100, Tz-You 1st Road, Kaohsiung 807, Taiwan.
Sashida G
Ito Y
Kodama A
Fukutake K
Ohyashiki JH
Ohyashiki K
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2006 Mar; Vol. 165 (2), pp. 161-6.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Leukemia, Myeloid/*genetics
Mutagens/*toxicity
Myelodysplastic Syndromes/*genetics
Acute Disease ; Aged ; Aged, 80 and over ; Female ; Humans ; Leukemia, Myeloid/chemically induced ; Male ; Middle Aged ; Myelodysplastic Syndromes/chemically induced ; Prognosis
Czasopismo naukowe
Tytuł:
Dup(1)(p31.2p36.2) in acute myelomonocytic leukemia.
Autorzy:
Wong KF
Wong ML
Tu SP
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2006 Feb; Vol. 165 (1), pp. 83-4.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Gene Duplication*
Leukemia, Myelomonocytic, Acute/*genetics
Adult ; Chromosome Banding ; Chromosome Mapping ; DNA-Binding Proteins/genetics ; Female ; Humans ; Transcription Factors/genetics
Raport
Tytuł:
Constitutional partial 1q trisomy mosaicism and Wilms tumor.
Autorzy:
Mark HF; Center for Human Genetics, Boston University School of Medicine, MA 02118, USA. />Wyandt H
Pan A
Milunsky JM
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Oct 15; Vol. 162 (2), pp. 166-71.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Mosaicism*
Trisomy*
Abnormalities, Multiple/*genetics
Wilms Tumor/*genetics
Child, Preschool ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Intellectual Disability/genetics ; Karyotyping ; Wilms Tumor/complications
Czasopismo naukowe
Tytuł:
Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9).
Autorzy:
Sambani C; Laboratory of Health Physics & Environmental Hygiene, NCSR Demokritos, 15310 Aghia Paraskevi, Athens, Greece. />La Starza R
Pierini V
Vandenberghe P
Gonzales-Aguilera JJ
Rigana H
Koumbi D
Manola KN
Stavropoulou C
Georgakakos VN
Pagoni M
Wlodarska I
Mecucci C
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Oct 01; Vol. 162 (1), pp. 45-9.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 9*
Translocation, Genetic*
Myeloproliferative Disorders/*genetics
Aged ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Identification of oligodendroglioma specific chromosomal copy number changes in the glioblastoma MI-4 cell line by array-CGH and FISH analyses.
Autorzy:
Magnani I; Department of Biology and Genetics, University of Milan, via Viotti3/5, 20133 Milan, Italy.
Moroni RF
Roversi G
Beghini A
Pfundt R
Schoenmakers EF
Larizza L
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Sep; Vol. 161 (2), pp. 140-5.
Typ publikacji:
Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cell Line, Tumor*
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Brain Neoplasms/*genetics
Glioblastoma/*genetics
Oligodendroglioma/*genetics
Chromosomes, Human, Pair 19 ; Gene Dosage ; Humans ; In Situ Hybridization, Fluorescence ; Microarray Analysis
Czasopismo naukowe
Tytuł:
Jumping translocations in multiple myeloma.
Autorzy:
Jamet D; Laboratoire d'Histologie, Embryologie et Cytogénétique, Faculté de Médecine et des Sciences de la Santé, Université de Bretagne Occidentale, 22 Avenue Camille Desmoulins, Brest cedex F-29285, France.
Marzin Y
Douet-Guilbert N
Morel F
Le Bris MJ
Herry A
Banzakour S
Bourquard P
Morice P
Abgrall JF
Berthou C
De Braekeleer M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Sep; Vol. 161 (2), pp. 159-63.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Translocation, Genetic*
Multiple Myeloma/*genetics
Aged ; Female ; Humans ; In Situ Hybridization, Fluorescence/methods ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
A der(14)t(1;14)(q12;p11) in chronic myelomonocytic leukemia.
Autorzy:
Djordjevic V; Institute of Hematology, Clinical Center of Serbia, Koste Todorovića 2, 11000 Belgrade, Serbia and Montenegro. />Jankovic G
Suvajdzic N
Marisavljevic D
Pantic M
Bogdanovic A
Sefer D
Dencic M
Colovic M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Jul 01; Vol. 160 (1), pp. 89-93.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 14*
Translocation, Genetic*
Leukemia, Myelomonocytic, Chronic/*genetics
Adult ; Humans ; Male ; Trisomy
Czasopismo naukowe
Tytuł:
Molecular cytogenetic analysis of chromosomes 1 and 19 in glioma cell lines.
Autorzy:
Law ME; Department of Laboratory Medicine and Pathology, Division of Laboratory Genetics, Mayo Clinic and Foundation, 200 First Street SW, Rochester, MN 55905, USA.
Templeton KL
Kitange G
Smith J
Misra A
Feuerstein BG
Jenkins RB
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Jul 01; Vol. 160 (1), pp. 1-14.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Loss of Heterozygosity*
Glioma/*genetics
Cell Line, Tumor ; Humans ; In Situ Hybridization, Fluorescence ; PTEN Phosphohydrolase ; Phosphoric Monoester Hydrolases/genetics ; Polymerase Chain Reaction ; Tumor Suppressor Proteins/genetics
Czasopismo naukowe
Tytuł:
Inv(1)(p22q25) in chronic myeloproliferative disease: constitutional or clonal defect?
Autorzy:
Wong KF; Department of Pathology, Queen Elizabeth Hospital, 30 Gascoigne Road, Hong Kong SAR, China. />Wong WC
Cheuk W
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Apr 15; Vol. 158 (2), pp. 188-91.
Typ publikacji:
Case Reports; Journal Article; Review
MeSH Terms:
Chromosome Inversion*
Chromosomes, Human, Pair 1*
Myeloproliferative Disorders/*genetics
Aged ; Chromosome Banding ; Humans ; Karyotyping ; Male ; Middle Aged ; Myeloproliferative Disorders/pathology
Czasopismo naukowe
Tytuł:
Translocation (1;4;12)(q25;q27;q15) in a childhood intramuscular lipoma.
Autorzy:
Bao L
Miles L
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Apr 01; Vol. 158 (1), pp. 95-7.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 12*
Chromosomes, Human, Pair 4*
Translocation, Genetic*
Lipoma/*genetics
Muscle Neoplasms/*genetics
Child ; Female ; Humans ; Karyotyping
Raport
Tytuł:
Jumping translocation of 1q in a BCR/ABL-positive acute lymphoblastic leukemia.
Autorzy:
Pelz AF; Institute of Human Genetics, Otto-von-Guericke University of Magdeburg, Leipziger Strasse 44, H.26, D-39120 Magdeburg, Germany. />Müller G
Wieacker P
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Mar; Vol. 157 (2), pp. 157-9.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Translocation, Genetic*
Fusion Proteins, bcr-abl/*metabolism
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Aged ; Chromosomes, Human, Pair 22 ; Chromosomes, Human, Pair 3 ; Chromosomes, Human, Pair 8 ; Humans ; Karyotyping ; Male
Czasopismo naukowe
Tytuł:
Rearrangement of the MLL gene in acute myeloblastic leukemia: report of two rare translocations.
Autorzy:
Douet-Guilbert N; Laboratoire d'Histologie, Embryologie et Cytogénétique, Faculté de Médecine et des Sciences de la Santé, Université de Bretagne Occidentale 22, avenue Camille Desmoulins CS 93837, F-29238, Brest cedex 3, France.
Morel F
Le Bris MJ
Herry A
Morice P
Bourquard P
Banzakour S
Le Calvez G
Marion V
Berthou C
De Braekeleer M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Mar; Vol. 157 (2), pp. 169-74.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 11*
Chromosomes, Human, Pair 17*
Translocation, Genetic*
DNA-Binding Proteins/*genetics
Leukemia, Myeloid, Acute/*genetics
Proto-Oncogenes/*genetics
Transcription Factors/*genetics
Adult ; Histone-Lysine N-Methyltransferase ; Humans ; Karyotyping ; Male ; Middle Aged ; Myeloid-Lymphoid Leukemia Protein
Czasopismo naukowe
Tytuł:
Molecular cytogenetic study of instability at 1q21 approximately q32 in adult acute lymphoblastic leukemia.
Autorzy:
Specchia G; Hematology, University of Foggia, Foggia, Italy. />Albano F
Anelli L
Zagaria A
Liso A
Pannunzio A
Archidiacono N
Liso V
Rocchi M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Jan 01; Vol. 156 (1), pp. 54-8.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Middle Aged ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology
Czasopismo naukowe
Tytuł:
Cytogenetic abnormalities in hepatoblastoma: report of two new cases and review of the literature suggesting imbalance of chromosomal regions on chromosomes 1, 4, and 12.
Autorzy:
Nagata T; Department of Advanced Medicine, Nihon University, School of Medicine, 30-1 Oyaguchikami-cho, Itabashi-ku, Tokyo 173-8610, Japan. />Nakamura M
Shichino H
Chin M
Sugito K
Ikeda T
Koshinaga T
Fukuzawa M
Inoue M
Mugishima H
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Jan 01; Vol. 156 (1), pp. 8-13.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 12*
Chromosomes, Human, Pair 4*
Hepatoblastoma/*genetics
Liver Neoplasms/*genetics
Aneuploidy ; Child, Preschool ; Female ; Humans ; Infant ; Male ; Translocation, Genetic
Czasopismo naukowe
Tytuł:
Identification of a novel t(1;9)(q11;q34) in acute myelocytic leukemia.
Autorzy:
Piccaluga PP
Luatti S
Ascani S
Bianchini M
Malagola M
Rondoni M
Gaitani S
Testoni N
Pileri SA
Baccarani M
Martinelli G
Visani G
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2004 May; Vol. 151 (1), pp. 85-6.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 9*
Translocation, Genetic*
Leukemia, Myeloid, Acute/*genetics
Female ; Humans ; Immunophenotyping ; Karyotyping ; Leukemia, Myeloid, Acute/immunology ; Middle Aged
Raport
Tytuł:
Genetic and pathologic significance of 1p, 17p, and 18q aneusomy and the ERBB2 gene in colorectal cancer and related normal colonic mucosa.
Autorzy:
Cianciulli A; Department of Clinical Pathology, Regina Elena Cancer Institute, IFO Via Elio Chianesi 53, 00144 Rome, Italy. />Cosimelli M
Marzano R
Merola R
Piperno G
Sperduti I
de la Iglesia F
Leonardo G
Graziano F
Mancini R
Guadagni F
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2004 May; Vol. 151 (1), pp. 52-9.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 17*
Chromosomes, Human, Pair 18*
Genes, erbB-2*
Colon/*metabolism
Colorectal Neoplasms/*genetics
Adult ; Aged ; Aged, 80 and over ; Female ; Gene Amplification ; Humans ; In Situ Hybridization, Fluorescence ; Intestinal Mucosa/metabolism ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Association of loss of 1p and alterations of chromosome 14 in meningioma progression.
Autorzy:
Lopez-Gines C; Department of Pathology, Medical School, University of Valencia, Avda. Blasco Ibáñez 17, 46010 Valencia, Spain. />Cerda-Nicolas M
Gil-Benso R
Callaghan R
Collado M
Roldan P
Llombart-Bosch A
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2004 Jan 15; Vol. 148 (2), pp. 123-8.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 14*
Meningioma/*genetics
Adult ; Aged ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Middle Aged ; Monosomy
Czasopismo naukowe
Tytuł:
Centromeric transverse fission of chromosome 1 in a case of acute myelocytic leukemia.
Autorzy:
Bakshi SR
Roy SK
Patel SJ
Trivedi PJ
Brahmbhatt M
Patel SM
Shah PM
Patel DD
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Oct 15; Vol. 146 (2), pp. 173-5.
Typ publikacji:
Letter
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Leukemia, Myeloid, Acute/*genetics
Humans ; Karyotyping ; Male ; Middle Aged
Opinia redakcyjna
Tytuł:
A novel translocation der(4)t(1;4)(q21;q35) and a marker chromosome in a case of myelodysplastic syndrome.
Autorzy:
Vundinti BR
Madkaikar M
Kerketta L
Jijina F
Ghosh K
Mohanty D
Jijina F
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Jul 15; Vol. 144 (2), pp. 175-6.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 4*
Translocation, Genetic*
Myelodysplastic Syndromes/*genetics
Adult ; Humans ; Male
Raport
Tytuł:
Loss of 1p and 7p in radiation-induced meningiomas identified by comparative genomic hybridization.
Autorzy:
Rajcan-Separovic E; Cytogenetics Laboratory, Department of Pathology, University of British Columbia, BC Children's Hospital, Vancouver, BC, Canada. />Maguire J
Loukianova T
Nisha M
Kalousek D
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Jul 01; Vol. 144 (1), pp. 6-11.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Meningioma/*genetics
Neoplasms, Radiation-Induced/*genetics
Nucleic Acid Hybridization/*methods
Adult ; Aged ; Base Sequence ; DNA Primers ; Female ; Humans ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Interphase cytogenetic characterization of aberrations in the long arm of chromosome 1 in B-cell lymphoid malignancies.
Autorzy:
Weng L
Gesk S
Martín-Subero JI
Harder L
Schlegelberger B
Grote W
Siebert R
Dyer MJ
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Jul 01; Vol. 144 (1), pp. 83-4.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Interphase*
Lymphoma, B-Cell/*genetics
Humans ; In Situ Hybridization, Fluorescence
Raport
Tytuł:
Detection by fluorescence in situ hybridization of microdeletions at 1p36 in lymphomas, unidentified on cytogenetic analysis.
Autorzy:
Rajgopal A; Molecular Medicine Unit, St. James's University Hospital, Leeds LS9 7TF, UK.
Carr IM
Leek JP
Hodge D
Bell SM
Roberts P
Horgan K
Bonthron DT
Selby PJ
Markham AF
MacLennan KA
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Apr 01; Vol. 142 (1), pp. 46-50.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
In Situ Hybridization, Fluorescence/*methods
Lymphoma/*genetics
Adolescent ; Adult ; Aged ; Cytogenetic Analysis ; Female ; Humans ; Male ; Middle Aged ; Sensitivity and Specificity
Czasopismo naukowe
Tytuł:
A consistent region of deletion on 1p36 in meningiomas: identification and relation to malignant progression.
Autorzy:
Murakami M; Department of Neurosurgery, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Hashimoto N
Takahashi Y
Hosokawa Y
Inazawa J
Mineura K
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Jan 15; Vol. 140 (2), pp. 99-106.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1/*ultrastructure
Meningeal Neoplasms/*genetics
Meningioma/*genetics
Adult ; Aged ; Alleles ; Biomarkers, Tumor/analysis ; Chromosomes, Human, Pair 1/genetics ; Disease Progression ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Ki-67 Antigen/analysis ; Ki-67 Antigen/genetics ; Loss of Heterozygosity ; Male ; Meningeal Neoplasms/pathology ; Meningioma/pathology ; Microsatellite Repeats ; Middle Aged ; Neoplasm Proteins/analysis ; Neoplasm Proteins/genetics
Czasopismo naukowe
Tytuł:
Structural chromosomal abnormality of 1q in acute leukemia with Sweet syndrome.
Autorzy:
Colovic M
Jankovic G
Suvajdzic N
Nikolic M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2002 Nov; Vol. 139 (1), pp. 84-5.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Leukemia, Myeloid, Acute/*genetics
Sweet Syndrome/*genetics
Adult ; Chromosome Banding ; Chromosome Mapping ; Female ; Humans ; Karyotyping ; Leukemia, Myeloid, Acute/complications ; Leukemia, Myeloid, Acute/pathology ; Sweet Syndrome/complications ; Sweet Syndrome/pathology
Raport
Tytuł:
Late appearance of t(1;19)(q11;q11) in myelodysplastic syndrome associated with dysplastic eosinophilia and pulmonary alveolar proteinosis.
Autorzy:
Ando J; Department of Hematology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Tamayose K
Sugimoto K
Oshimi K
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2002 Nov; Vol. 139 (1), pp. 14-7.
Typ publikacji:
Case Reports; Journal Article; Review
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Translocation, Genetic*
Eosinophilia/*genetics
Myelodysplastic Syndromes/*genetics
Pulmonary Alveolar Proteinosis/*genetics
Bone Marrow Cells/pathology ; Chromosome Mapping ; DNA/blood ; DNA/genetics ; Eosinophilia/complications ; Eosinophilia/pathology ; Eosinophils/pathology ; Humans ; Karyotyping ; Male ; Metaphase ; Middle Aged ; Myelodysplastic Syndromes/complications ; Myelodysplastic Syndromes/pathology ; Pulmonary Alveolar Proteinosis/complications ; Pulmonary Alveolar Proteinosis/pathology
Czasopismo naukowe
Tytuł:
Partial deletion of chromosome 1 in a case of acute myelocytic leukemia.
Autorzy:
Coupland LA; Department of Clinical Haematology, The Canberra Hospital, Garran, Australia. />Jammu V
Pidcock ME
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2002 Nov; Vol. 139 (1), pp. 60-2.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Leukemia, Myeloid, Acute/*genetics
Adult ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Humans ; Karyotyping ; Leukemia, Myeloid, Acute/drug therapy ; Leukemia, Myeloid, Acute/pathology ; Male ; Time Factors ; Treatment Outcome
Czasopismo naukowe
Tytuł:
Precursor T-lymphoblastic leukemia with a novel t(1;22)(p34;q13).
Autorzy:
Wong KF; Department of Pathology, Queen Elizabeth Hospital, 30 Gascoigne Road, Kowloon, Hong Kong SAR, China. />So CC
Lau G
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2002 Jul 15; Vol. 136 (2), pp. 146-8.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Translocation, Genetic*
Leukemia, Lymphoid/*genetics
Adult ; Chromosomes, Human, Pair 22 ; Female ; Humans ; Karyotyping
Czasopismo naukowe
Tytuł:
A novel dic(1;10) in a patient with myelodysplastic syndrome.
Autorzy:
Sambani C; Laboratory of Health Physics & Environmental Hygiene, NCSR Demokritos, Athens, Greece. />La Starza R
Stavropoulou C
Manola KN
Harhalakis N
Mecucci C
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2002 Feb; Vol. 133 (1), pp. 87-9.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 10*
Monosomy*
Trisomy*
Myelodysplastic Syndromes/*genetics
Adult ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male
Czasopismo naukowe
Tytuł:
Novel der(1)t(1;19) in two patients with myeloid neoplasias.
Autorzy:
Tchinda J; Institut für Humangenetik, Westfälische Wilhelms-Universität, Vesaliusweg 12-14, Münster, Germany. />Volpert S
Neumann T
Kennerknecht I
Ritter J
Büchner T
Berdel WE
Horst J
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2002 Feb; Vol. 133 (1), pp. 61-5.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Translocation, Genetic*
Anemia, Sideroblastic/*genetics
Leukemia, Monocytic, Acute/*genetics
Myelodysplastic Syndromes/*genetics
Adult ; Anemia, Sideroblastic/complications ; Fanconi Anemia/complications ; Fanconi Anemia/genetics ; Female ; Genetic Markers ; Humans ; Infant ; Karyotyping ; Myelodysplastic Syndromes/complications
Czasopismo naukowe
Tytuł:
Predominance of trisomy 1q in myelodysplastic syndromes in Korea: is there an ethnic difference? A 3-year multi-center study.
Autorzy:
Lee DS; Department of Clinical Pathology, Seoul National University College of Medicine, 28 Yongun-dong, Chongro-gu, 110-744, Seoul, South Korea.
Kim SH
Seo EJ
Park CJ
Chi HS
Ko EK
Yoon BH
Kim WH
Cho HI
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2002 Jan 15; Vol. 132 (2), pp. 97-101.
Typ publikacji:
Journal Article; Multicenter Study
MeSH Terms:
Chromosomes, Human, Pair 1*
Trisomy*
Myelodysplastic Syndromes/*ethnology
Myelodysplastic Syndromes/*genetics
Humans ; In Situ Hybridization, Fluorescence ; Korea
Czasopismo naukowe
Tytuł:
Application of molecular cytogenetic techniques in a case study of human cutaneous metastatic melanoma.
Autorzy:
Wiltshire RN; Cancer Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Dennis TR
Sondak VK
Meltzer PS
Trent JM
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2001 Dec; Vol. 131 (2), pp. 97-103.
Typ publikacji:
Case Reports; Comparative Study; Journal Article
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 8*
Melanoma/*genetics
Skin Neoplasms/*genetics
Aged ; Chromosome Banding ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Lymphatic Metastasis ; Melanoma/pathology ; Skin Neoplasms/pathology
Czasopismo naukowe
Tytuł:
Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics.
Autorzy:
Granzow M; Institute of Human Genetics, University of Heidelberg, Im Neuenheimer Feld 328, D-69120, Heidelberg, Germany.
Popp S
Weber S
Schoell B
Holtgreve-Grez H
Senf L
Hager D
Boschert J
Scheurlen W
Jauch A
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2001 Oct 01; Vol. 130 (1), pp. 79-83.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Brain Neoplasms/*genetics
Ependymoma/*genetics
Child, Preschool ; Humans ; In Situ Hybridization, Fluorescence ; Male
Czasopismo naukowe
Tytuł:
Comparative genomic hybridization analysis identifies gains of 1p35 approximately p36 and chromosome 19 in osteosarcoma.
Autorzy:
Zielenska M; Department of Laboratory Medicine and Pathobiology, University of Toronto, Princess Margaret Hospital, Toronto, Ontario, Canada.
Bayani J
Pandita A
Toledo S
Marrano P
Andrade J
Petrilli A
Thorner P
Sorensen P
Squire JA
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2001 Oct 01; Vol. 130 (1), pp. 14-21.
Typ publikacji:
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Nucleic Acid Hybridization*
Bone Neoplasms/*genetics
Osteosarcoma/*genetics
Genome ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping
Czasopismo naukowe
Tytuł:
Analysis of p73 gene in meningiomas with deletion at 1p.
Autorzy:
Lomas J; Laboratorio de Oncogenética Molecular, Unidad de Investigación, Departamento de Cirugía Experimental, Hospital Universitario La Paz, Paseo Castellana 261, 28046 Madrid, Spain.
Bello MJ
Arjona D
Gonzalez-Gomez P
Alonso ME
de Campos JM
Vaquero J
Ruiz-Barnes P
Sarasa JL
Casartelli C
Rey JA
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2001 Aug; Vol. 129 (1), pp. 88-91.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Genes, Tumor Suppressor*
DNA-Binding Proteins/*genetics
Meningeal Neoplasms/*genetics
Meningioma/*genetics
Nuclear Proteins/*genetics
Humans ; Tumor Protein p73 ; Tumor Suppressor Proteins
Czasopismo naukowe
Tytuł:
A highly aggressive primitive mesenchymal tumor with a translocation (1;19)(q12;q13.2).
Autorzy:
Lui W; Department of Molecular Medicine, Endocrine Tumor Unit, Karolinska Hospital, SE-171 76 Stockholm, Sweden.
Wejde J
Tani E
Brosjö O
Kytölä S
Larsson C
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2001 Jun; Vol. 127 (2), pp. 128-33.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Translocation, Genetic*
Mesenchymoma/*genetics
Amputation, Surgical ; Biopsy, Needle ; Chromosome Mapping ; Diagnosis, Differential ; Finland ; Foot ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Mesenchymoma/pathology ; Mesenchymoma/surgery ; Middle Aged ; Neoplasm Metastasis ; Rhabdomyosarcoma/genetics ; Rhabdomyosarcoma/pathology ; Sarcoma/genetics ; Sarcoma/pathology ; Sweden ; White People
Czasopismo naukowe
Tytuł:
Genetic rationale for microheterogeneity of human diphosphoinositol polyphosphate phosphohydrolase type 2.
Autorzy:
Caffrey JJ; InforMax Inc., 7600 Wisconsin Ave., Bethesda, MD 20814, USA.
Shears SB
Pokaż więcej
Źródło:
Gene [Gene] 2001 May 16; Vol. 269 (1-2), pp. 53-60.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 12*
Genetic Heterogeneity*
Acid Anhydride Hydrolases/*genetics
Cell Line ; Chromosome Mapping ; Colon ; Gene Expression ; Humans ; Isoenzymes/genetics ; Pseudogenes ; RNA, Messenger
Czasopismo naukowe
Tytuł:
Functional analysis of the promoter and chromosomal localization for human LEP503, a novel lens epithelium gene.
Autorzy:
Wen Y; The Membrane Biology Laboratory, Department of Physiology, School of Medicine, UCLA, Los Angeles, CA 90073, USA. />Ibaraki N
Reddy VN
Sachs G
Pokaż więcej
Źródło:
Gene [Gene] 2001 May 16; Vol. 269 (1-2), pp. 61-71.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
MeSH Terms:
Chromosomes, Human, Pair 1*
Lens, Crystalline*
Promoter Regions, Genetic*
Crystallins/*genetics
Amino Acid Sequence ; Animals ; Base Sequence ; Binding Sites ; CHO Cells ; Cell Line ; Chromosome Mapping ; Cricetinae ; Crystallins/biosynthesis ; DNA-Binding Proteins ; Humans ; Molecular Sequence Data ; Rats ; Transcription, Genetic
Czasopismo naukowe
Tytuł:
BCL10 is not a major target for frequent loss of 1p in testicular germ cell tumors.
Autorzy:
Kakinuma H; Department of Urology, Akita University School of Medicine, 1-1-1 Hondo, 010-8543, Akita, Japan.
Habuchi T
Ito T
Mishina M
Sato K
Satoh S
Akao T
Ogawa O
Kato T
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2001 Apr 15; Vol. 126 (2), pp. 134-8.
Typ publikacji:
Journal Article
MeSH Terms:
Adaptor Proteins, Signal Transducing*
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Neoplasm Proteins/*genetics
Neoplasms, Germ Cell and Embryonal/*genetics
Testicular Neoplasms/*genetics
B-Cell CLL-Lymphoma 10 Protein ; Base Sequence ; DNA Primers ; Humans ; Loss of Heterozygosity ; Male ; Mutation ; Polymorphism, Single-Stranded Conformational
Czasopismo naukowe
Tytuł:
Cytogenetic instability, predominantly involving chromosome 1, is characteristic of elastofibroma.
Autorzy:
McComb EN; Departments of Pathology and Microbiology, University of Nebraska Medical Center, 68198-3135, Omaha, NE, USA.
Feely MG
Neff JR
Johansson SL
Nelson M
Bridge JA
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2001 Apr 01; Vol. 126 (1), pp. 68-72.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Fibroma/*genetics
Aged ; Female ; Fibroma/pathology ; Humans ; Karyotyping ; Middle Aged
Czasopismo naukowe
Tytuł:
Fifteen cases of t(1;19)(q23;p13.3) identified in an Australian series of 122 children and 80 adults with acute lymphoblastic leukemia.
Autorzy:
Sharma P; Department of Cytogenetics, NCH, Royal Alexandra Hospital for Children, Westmead 2145, Australia.
Watson N
Sartor M
McCowage G
Smith A
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2001 Jan 15; Vol. 124 (2), pp. 132-6.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Translocation, Genetic*
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Adolescent ; Adult ; Australia ; Bone Marrow Cells/physiology ; Child ; Child, Preschool ; Female ; Humans ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Acute megakaryoblastic leukemia in an infant with a novel t(1;9)(p32;q34).
Autorzy:
Hasegawa D; Department of Pediatrics, Kobe University School of Medicine, Japan.
Sano K
Kosaka Y
Hayakawa A
Kawagoe R
Kawasaki K
Nakamura H
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2000 Oct 01; Vol. 122 (1), pp. 59-62.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 9*
Translocation, Genetic*
Blood Platelets/*enzymology
Leukemia, Megakaryoblastic, Acute/*genetics
Bone Marrow/enzymology ; Bone Marrow/ultrastructure ; Female ; Flow Cytometry ; Humans ; Infant ; Karyotyping ; Microscopy, Electron ; Peroxidases/metabolism
Czasopismo naukowe
Tytuł:
High-resolution analysis of chromosome arm 1p alterations in meningioma.
Autorzy:
Bello MJ; Laboratorio de Oncogenética Molecular, Department of Cirugía Experimental, Hospital Universitario La Paz, Madrid, Spain.
de Campos JM
Vaquero J
Kusak ME
Sarasa JL
Rey JA
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2000 Jul 01; Vol. 120 (1), pp. 30-6.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Loss of Heterozygosity*
Brain Neoplasms/*genetics
Meningioma/*genetics
Humans ; Microsatellite Repeats
Czasopismo naukowe
Tytuł:
Duplication of 1q in a child with down syndrome and myelodysplastic syndrome.
Autorzy:
Blann MM; Department of Pathology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Morgan DL
Oblender M
Heinen B
Williams J
Tonk VS
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2000 May; Vol. 119 (1), pp. 74-6.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Anemia, Refractory, with Excess of Blasts/*genetics
Down Syndrome/*genetics
Anemia, Refractory, with Excess of Blasts/complications ; Anemia, Refractory, with Excess of Blasts/drug therapy ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Child, Preschool ; Down Syndrome/complications ; Humans ; Karyotyping ; Lymphocyte Activation ; Male
Czasopismo naukowe
Tytuł:
A case of papillary meningioma with a t(1;4)(q44;q21).
Autorzy:
Go Y; Department of Pathology, Fukuoka University School of Medicine, Fukuoka, Japan.
Ohjimi Y
Iwasaki H
Oka K
Ishiguro M
Kaneko Y
Tsuchimochi H
Tomonaga M
Kikuchi M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2000 May; Vol. 119 (1), pp. 37-41.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 4*
Translocation, Genetic*
Meningioma/*genetics
Adult ; Chromosome Banding ; Female ; Humans ; Karyotyping ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
High frequency of loss of heterozygosity for 1p35-p36 (D1S247) in Wilms tumor.
Autorzy:
Steinberg R; Department of Pediatric Surgery, Tel Aviv, Israel.
Freud E
Zer M
Ziperman I
Goshen Y
Ash S
Stein J
Zaizov R
Avigad S
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2000 Mar; Vol. 117 (2), pp. 136-9.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Loss of Heterozygosity*
Kidney Neoplasms/*genetics
Wilms Tumor/*genetics
Child ; Child, Preschool ; Humans ; Infant ; Kidney Neoplasms/pathology ; Microsatellite Repeats ; Neoplasm Staging ; Wilms Tumor/pathology
Czasopismo naukowe
Tytuł:
Analysis of MLL-derived transcripts in infant acute monocytic leukemia with a complex translocation (1;11;4)(q21;q23;p16).
Autorzy:
So CW; Department of Pathology, University of Hong Kong, People's Republic of China.
Ma SK
Wan TS
Chan GC
Ha SY
Chan LC
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2000 Feb; Vol. 117 (1), pp. 24-7.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 11*
Chromosomes, Human, Pair 4*
Proto-Oncogenes*
Transcription Factors*
Translocation, Genetic*
DNA-Binding Proteins/*genetics
Leukemia, Monocytic, Acute/*genetics
Base Sequence ; Bone Marrow Transplantation ; DNA Primers ; Female ; Histone-Lysine N-Methyltransferase ; Humans ; Infant ; Karyotyping ; Leukemia, Monocytic, Acute/therapy ; Myeloid-Lymphoid Leukemia Protein
Czasopismo naukowe
Tytuł:
Molecular characterization of the human PEA15 gene on 1q21-q22 and association with type 2 diabetes mellitus in Pima Indians.
Autorzy:
Wolford JK; Clinical Diabetes and Nutrition Section, Phoenix Epidemiology and Research Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National institutes of Health, 4212 N. 16th Street, Phoenix, AZ 85016, USA. />Bogardus C
Ossowski V
Prochazka M
Pokaż więcej
Źródło:
Gene [Gene] 2000 Jan 04; Vol. 241 (1), pp. 143-8.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Asian People/*genetics
Diabetes Mellitus, Type 2/*genetics
Indians, North American/*genetics
Protein Kinase C/*genetics
Alleles ; Alu Elements ; Base Sequence ; Chromosomes, Artificial, Yeast ; Exons ; Genetic Linkage ; Genotype ; Humans ; Introns ; Models, Genetic ; Molecular Sequence Data ; Polymorphism, Single Nucleotide ; Promoter Regions, Genetic
Czasopismo naukowe
Tytuł:
Involvement of chromosomes 1 and 18 in renal cell tumors.
Autorzy:
Dal Cin P; Center for Human Genetics, University of Leuven, Belgium.
Roskams T
De Vos R
Van Poppel H
Balzarini P
Van Den Berghe H
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2000 Jan 01; Vol. 116 (1), pp. 54-8.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Carcinoma, Renal Cell/*genetics
Kidney Neoplasms/*genetics
Aged ; Carcinoma, Renal Cell/pathology ; Chromosomes, Human, Pair 18 ; Eosinophils/pathology ; Female ; Gene Deletion ; Humans ; Karyotyping ; Kidney Neoplasms/pathology ; Male ; Middle Aged ; Monosomy
Czasopismo naukowe
Tytuł:
Deletion (1)(q12) and double minutes in a metastatic adenocarcinoma of the prostate.
Autorzy:
Carvalho-Salles AB; Departmento de Biologia, Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Preto, Brazil.
Mesquita JC
Tajara EH
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2000 Jan 01; Vol. 116 (1), pp. 50-3.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Gene Deletion*
Neoplasm Metastasis*
Adenocarcinoma/*genetics
Prostatic Neoplasms/*genetics
Aged ; Humans ; Karyotyping ; Male ; Ploidies ; Ring Chromosomes ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł:
der(11)t(1;11)(q11;p15) as an additional cytogenetic abnormality in Ph+ adult acute lymphoblastic leukemia.
Autorzy:
Ma SK
Wan TS
Chan LC
Yip SF
Yeung YM
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Dec; Vol. 115 (2), pp. 134-5.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 11*
Philadelphia Chromosome*
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Adult ; Antineoplastic Agents/therapeutic use ; Humans ; Karyotyping ; Male ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy ; Translocation, Genetic
Raport
Tytuł:
Trisomy 2 and 19, and tetrasomy 1q and 14 in hepatoblastoma.
Autorzy:
Park JP
Ornvold KT
Brown AM
Mohandas TK
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Nov; Vol. 115 (1), pp. 86-7.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 14*
Chromosomes, Human, Pair 19*
Chromosomes, Human, Pair 2*
Hepatoblastoma/*genetics
Liver Neoplasms/*genetics
Aneuploidy ; Chromosome Banding ; Humans ; Infant ; Karyotyping ; Male ; Trisomy
Raport
Tytuł:
Nasopharyngeal teratoma and mosaic tetrasomy 1q detected at amniocentesis. A case report and review of the literature.
Autorzy:
Beverstock GC; Department of Clinical Cytogenetics, Leiden University Medical Centre, The Netherlands.
Mollevanger P
Baaij M
Lind J
van Ieperen L
Bartelings MM
Teunissen K
Brandenburg H
Van Opstal D
Los F
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Nov; Vol. 115 (1), pp. 11-8.
Typ publikacji:
Case Reports; Journal Article; Review
MeSH Terms:
Amniocentesis*
Aneuploidy*
Chromosomes, Human, Pair 1*
Fetal Diseases/*genetics
Nasopharyngeal Neoplasms/*genetics
Teratoma/*genetics
Adult ; Chromosome Aberrations ; Chromosome Banding ; Female ; Fetal Diseases/diagnostic imaging ; Humans ; In Situ Hybridization, Fluorescence ; Nasopharyngeal Neoplasms/diagnostic imaging ; Polyhydramnios ; Pregnancy ; Pregnancy Trimester, Second ; Teratoma/diagnostic imaging ; Ultrasonography
Czasopismo naukowe
Tytuł:
Derivative (1;7)(q10;p10) in a patient with de novo acute erythroblastic leukemia (AML-M6).
Autorzy:
Obara N; Department of Medicine, Tsukuba Memorial Hospital, Japan.
Shinagawa A
Komatsu T
Abe T
Ninomiya H
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Nov; Vol. 115 (1), pp. 62-4.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Translocation, Genetic*
Leukemia, Erythroblastic, Acute/*genetics
Aged ; Bone Marrow Cells/pathology ; Humans ; Karyotyping ; Leukemia, Erythroblastic, Acute/pathology ; Lymphocyte Subsets ; Male
Czasopismo naukowe
Tytuł:
Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1q.
Autorzy:
Scheres JM; Division of Medical Genetics, University Medical Center Utrecht, The Netherlands.
de Pater JM
Stoutenbeek P
Wijmenga C
Rosenberg C
Pearson PL
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Nov; Vol. 115 (1), pp. 1-10.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Isochromosomes*
Fetal Diseases/*genetics
Mouth Neoplasms/*genetics
Skull Neoplasms/*genetics
Teratoma/*genetics
Alleles ; Female ; Fetal Diseases/pathology ; Gestational Age ; Humans ; In Situ Hybridization, Fluorescence ; Mitosis ; Models, Genetic ; Mouth Neoplasms/diagnostic imaging ; Mouth Neoplasms/pathology ; Polymorphism, Genetic ; Pregnancy ; Sex Factors ; Skull Neoplasms/diagnostic imaging ; Skull Neoplasms/pathology ; Teratoma/diagnostic imaging ; Teratoma/pathology ; Ultrasonography, Prenatal
Czasopismo naukowe
Tytuł:
Translocation (X;1) associated with a nonpapillary carcinoma in a young woman: a new definition for an Xp11.2 RCC subtype.
Autorzy:
Désangles F; Pathology and Cytogenetic Laboratory, Val de Grâce Hospital, Paris, France.
Camparo P
Fouet C
Houlgatte A
Arborio M
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Sep; Vol. 113 (2), pp. 141-4.
Typ publikacji:
Case Reports; Journal Article; Review
MeSH Terms:
Chromosomes, Human, Pair 1*
Translocation, Genetic*
X Chromosome*
Carcinoma, Renal Cell/*genetics
Kidney Neoplasms/*genetics
Adult ; Female ; Humans ; Male
Czasopismo naukowe
Tytuł:
Identification of a novel amplicon at 1q31 in pancreatic cancer cell lines.
Autorzy:
Tirado CA; Department of Zoology, Arizona State University, Tempe, USA.
Sandberg AA
Stone JF
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Sep; Vol. 113 (2), pp. 110-4.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Pancreatic Neoplasms/*genetics
Chromosome Banding/methods ; Chromosome Deletion ; Female ; Gene Amplification ; Humans ; In Situ Hybridization/methods ; Karyotyping ; Tumor Cells, Cultured ; X Chromosome
Czasopismo naukowe
Tytuł:
Complex rearrangement of chromosomes 1, 7, and 16 in chronic myelomonocytic leukemia.
Autorzy:
Fan YS
Rizkalla K
Barr RM
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Jul 15; Vol. 112 (2), pp. 190-2.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 16*
Chromosomes, Human, Pair 7*
Leukemia, Myelomonocytic, Chronic/*genetics
Chromosome Banding ; Humans ; Karyotyping ; Male ; Middle Aged
Raport
Tytuł:
DNA copy number losses at 1p32-pter in monozygotic twins concordant for breast cancer.
Autorzy:
el-Rifai W; Department of Medical Genetics, University of Helsinki, Finland.
Tarmo L
Hemmer S
Försti A
Pedersen N
Lichtenstein P
Ahlbom A
Söderberg M
Knuutila S
Hemminki K
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Jul 15; Vol. 112 (2), pp. 169-72.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Diseases in Twins*
Twins, Monozygotic*
Breast Neoplasms/*genetics
DNA, Neoplasm/*genetics
Base Sequence ; DNA Primers ; Humans ; Polymerase Chain Reaction
Czasopismo naukowe
Tytuł:
Trisomy 1q generating translocations in Wilms tumor.
Autorzy:
Betts DR; Department of Oncology, University Children's Hospital, Zürich, Switzerland.
Ilg EC
Oezahin H
von der Weid N
Niggli FK
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Jul 15; Vol. 112 (2), pp. 138-43.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Translocation, Genetic*
Trisomy*
Wilms Tumor/*genetics
Humans ; In Situ Hybridization, Fluorescence ; Karyotyping
Czasopismo naukowe
Tytuł:
Frequent alterations of evolutionarily conserved regions of chromosome 1 in human malignant melanoma.
Autorzy:
Zhang J; Cancer Genetics Branch, National Institutes of Health, Bethesda, MD 20892-4470, USA.
Glatfelter AA
Taetle R
Trent JM
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Jun; Vol. 111 (2), pp. 119-23.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosome Aberrations/*genetics
Melanoma/*genetics
Skin Neoplasms/*genetics
Animals ; Base Sequence ; Chromosome Disorders ; Chromosome Mapping ; Chromosomes, Artificial, Yeast ; Conserved Sequence ; Contig Mapping ; Humans ; In Situ Hybridization, Fluorescence ; Mice ; Sequence Tagged Sites ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł:
Acute myeloblastic leukemia (M0) with an unusual chromosomal abnormality: translocation (1;14)(p13;q32).
Autorzy:
Tecimer C; Department of Hematology/Medical Oncology, University of Louisville School of Medicine, Kentucky, USA.
Loy BA
Martin AW
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Jun; Vol. 111 (2), pp. 175-7.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 14*
Translocation, Genetic*
Leukemia, Myeloid, Acute/*genetics
Antigens, CD/metabolism ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Cytarabine/therapeutic use ; Female ; HLA-DR Antigens/metabolism ; Humans ; Idarubicin/therapeutic use ; Leukemia, Myeloid, Acute/drug therapy ; Leukemia, Myeloid, Acute/pathology ; Middle Aged ; Peroxidase/metabolism
Czasopismo naukowe
Tytuł:
A second known case of Down syndrome with t(1;18)(q25;q23) in leukemic cells.
Autorzy:
Brozek I
Babińska M
Limon J
Zaborowska-Sołtys M
Płoszyńska A
Balcerska A
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Apr 15; Vol. 110 (2), pp. 136-7.
Typ publikacji:
Case Reports; Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 18*
Translocation, Genetic*
Down Syndrome/*genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Child, Preschool ; Down Syndrome/complications ; Female ; Gene Frequency ; Humans ; Karyotyping
Raport
Tytuł:
Changes of chromosomes 1, 3, 6, and 11 in metastatic effusions arising from breast and ovarian cancer.
Autorzy:
Ioakim-Liossi A; Department of Pathology, Athens School of Medicine, University of Athens, Greece.
Gagos S
Athanassiades P
Athanassiadou P
Gogas J
Davaris P
Markopoulos C
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Apr; Vol. 110 (1), pp. 34-40.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 11*
Chromosomes, Human, Pair 3*
Chromosomes, Human, Pair 6*
Breast Neoplasms/*genetics
Ovarian Neoplasms/*genetics
Adult ; Aged ; Ascitic Fluid/genetics ; Female ; Humans ; Middle Aged ; Pleural Effusion/genetics
Czasopismo naukowe

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