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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

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