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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 :
Identification of a de novo microdeletion 1q44 in a patient with hypogenesis of the corpus callosum, seizures and microcephaly - A case report.
Autorzy :
Westphal DS; Institute of Human Genetics, Technical University Munich, Munich, Germany; Institute of Human Genetics, Helmholtz Zentrum Munich, Neuherberg, Germany. Electronic address: .
Andres S; Institute of Human Genetics, Technical University Munich, Munich, Germany.
Beitzel KI; Department of Diagnostic and Pediatric Radiology, Schwabing Hospital, Munich, Germany.
Makowski C; Department for Pediatrics, Technical University Munich, Munich, Germany.
Meitinger T; Institute of Human Genetics, Technical University Munich, Munich, Germany; Institute of Human Genetics, Helmholtz Zentrum Munich, Neuherberg, Germany.
Hoefele J; Institute of Human Genetics, Technical University Munich, Munich, Germany.
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Źródło :
Gene [Gene] 2017 Jun 15; Vol. 616, pp. 41-44. Date of Electronic Publication: 2017 Mar 21.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Sequence Deletion*
Agenesis of Corpus Callosum/*genetics
Chromosomes, Human, Pair 1/*genetics
Microcephaly/*genetics
Seizures/*genetics
Female ; Humans ; Infant ; Oligonucleotide Array Sequence Analysis ; Polymorphism, Single Nucleotide ; Repressor Proteins/genetics
Czasopismo naukowe
Tytuł :
Characterization of a novel acquired der(1)del(1)(p13p31)t(1;15)(q42;q15) in a high risk t(12;21)-positive acute lymphoblastic leukemia.
Autorzy :
Kjeldsen E; Hemodiagnostic Laboratory, Cancer Cytogenetics Section, Department of Hematology, Aarhus University Hospital, Tage-Hansens Gade 2, DK-8000 Aarhus C, Denmark. Electronic address: .
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Źródło :
Gene [Gene] 2016 Dec 20; Vol. 595 (1), pp. 39-48. Date of Electronic Publication: 2016 Sep 21.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Base Sequence*
Sequence Deletion*
Translocation, Genetic*
Chromosomes, Human, Pair 1/*genetics
Chromosomes, Human, Pair 15/*genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Adolescent ; Adult ; Humans ; Male
Czasopismo naukowe
Tytuł :
A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33.
Autorzy :
Wang J; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Fu C; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Zhang S; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Luo J; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Ouyang L; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Xie B; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Sun W; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
He S; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Su J; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Hu X; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Fei D; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Chen R; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Fan X; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Ou S; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China.
Chen S; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China. Electronic address: .
Shen Y; Laboratory of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region; Guangxi Birth Defects Prevention and Control Institute, Nanning 530003, Guangxi, People's Republic of China; Department of Laboratory Medicine, Department of Pathology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, United States; Claritas Genomics, Cambridge, MA 02139, United States. Electronic address: .
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Źródło :
Gene [Gene] 2016 Dec 05; Vol. 594 (1), pp. 59-65. Date of Electronic Publication: 2016 Aug 31.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Abnormalities, Multiple/*genetics
Chromosomes, Human, Pair 1/*genetics
Failure to Thrive/*genetics
Trisomy/*genetics
Chromosomes, Human, Pair 9/genetics ; Female ; Humans ; Infant, Low Birth Weight ; Infant, Newborn
SCR Disease Name :
Chromosome 9, trisomy 9q
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 :
Therapy-related, mixed phenotype acute leukemia with t(1;21)(p36;q22) and RUNX1 rearrangement.
Autorzy :
Yamamoto K; Department of Medicine, Kobe University Graduate School of Medicine, Chuo-ku, Japan. />Sada A
Kawano Y
Katayama Y
Shimoyama M
Matsui T
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Źródło :
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2010 Sep; Vol. 201 (2), pp. 122-7.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 21*
Gene Rearrangement*
Core Binding Factor Alpha 2 Subunit/*genetics
Leukemia, Myeloid, Acute/*genetics
Neoplasms, Second Primary/*genetics
Adult ; Antineoplastic Agents/therapeutic use ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Fatal Outcome ; Flow Cytometry ; Humans ; Immunophenotyping ; In Situ Hybridization, Fluorescence ; Karyotyping ; Leukemia, Myeloid, Acute/chemically induced ; Leukemia, Myeloid, Acute/diagnosis ; Male ; Neoplasms, Second Primary/chemically induced ; Neoplasms, Second Primary/diagnosis
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 :
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 :
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 :
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
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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 :
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
Pokaż więcej
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 :
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 :
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
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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

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