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


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:
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
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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
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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:
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
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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:
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
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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:
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:
Karyotypic characteristics of borderline malignant tumors of the ovary: trisomy 12, trisomy 7, and r(1) as nonrandom features.
Autorzy:
Pejovic T; Department of Gynecologic Oncology, University Hospital, Lund, Sweden.
Iosif CS
Mitelman F
Heim S
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1996 Dec; Vol. 92 (2), pp. 95-8.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 12*
Chromosomes, Human, Pair 7*
Trisomy*
Ovarian Neoplasms/*genetics
Adenocarcinoma, Mucinous/genetics ; Adenocarcinoma, Mucinous/pathology ; Carcinoma, Papillary/genetics ; Carcinoma, Papillary/pathology ; Chromosome Mapping ; Cystadenoma, Serous/genetics ; Cystadenoma, Serous/pathology ; Female ; Humans ; Karyotyping ; Neoplasm Staging ; Ovarian Neoplasms/pathology
Czasopismo naukowe
Tytuł:
An unusual cytogenetic abnormality involving chromosomes 1 and 7 in a case of chronic myelomonocytic leukemia.
Autorzy:
Papadhimitriou SI; Department of Clinical Hematology, Greek Cancer Institute, Athens, Greece.
Abazis D
Repa C
Papaconstantinou C
Papanastasiou C
Pangalos C
Stamatelou M
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1995 Nov; Vol. 85 (1), pp. 75-7.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Leukemia, Myelomonocytic, Chronic/*genetics
Aged ; Chromosome Inversion ; Gene Deletion ; Humans ; Karyotyping ; Male ; Trisomy
Czasopismo naukowe
Tytuł:
t(1;7)(p36;q32): a new recurring abnormality in primary myelodysplastic syndrome.
Autorzy:
Stefănescu DT; Department of Medical Genetics, Victor Babeş Institute, Bucharest, Romania.
Colită D
Nicoară S
Călin G
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1994 Jul 15; Vol. 75 (2), pp. 103-5.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Translocation, Genetic*
Anemia, Refractory, with Excess of Blasts/*genetics
Aged ; Humans ; Male
Czasopismo naukowe
Tytuł:
Unbalanced 1;7 translocation in myelodysplastic syndrome following treatment of acute myeloblastic leukemia with an 8;21 translocation.
Autorzy:
Hamamoto K; First Department of Internal Medicine, Kansai Medical University, Osaka, Japan.
Hashimoto-Ninomiya A
Kishimoto Y
Kimura T
Fujitake H
Yasunaga K
Horiike S
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1994 May; Vol. 74 (1), pp. 35-9.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 21*
Chromosomes, Human, Pair 7*
Chromosomes, Human, Pair 8*
Translocation, Genetic*
Anemia, Refractory, with Excess of Blasts/*genetics
Leukemia, Myeloid, Acute/*genetics
Adult ; Anemia, Refractory, with Excess of Blasts/chemically induced ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Humans ; Karyotyping ; Leukemia, Myeloid, Acute/drug therapy ; Male
Czasopismo naukowe
Tytuł:
Therapy-related myelodysplastic syndrome. Two cytogenetically unrelated abnormal clones in a patient with multiple myeloma.
Autorzy:
Abeliovich D; Department of Human Genetics, Mount Scopus, Hadassah University Hospital, Jerusalem, Israel.
Yehuda O
Ben-Neriah S
Matzner Y
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1993 Oct 15; Vol. 70 (2), pp. 117-9.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 5*
Chromosomes, Human, Pair 7*
Multiple Myeloma/*genetics
Myelodysplastic Syndromes/*genetics
Chromosome Deletion ; Chromosomes, Human, Pair 12 ; Chromosomes, Human, Pair 13 ; Humans ; Karyotyping ; Male ; Melphalan/adverse effects ; Melphalan/therapeutic use ; Middle Aged ; Multiple Myeloma/drug therapy ; Myelodysplastic Syndromes/chemically induced ; Translocation, Genetic
Czasopismo naukowe
Tytuł:
Cell lineage involvement in four patients with myelodysplastic syndrome and t(1;7) or trisomy 8 studied by simultaneous immunophenotyping and fluorescence in situ hybridization.
Autorzy:
Nylund SJ; Department of Medical Genetics, University of Helsinki, Finland.
Verbeek W
Larramendy ML
Ruutu T
Heinonen K
Hallman H
Knuutila S
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1993 Oct 15; Vol. 70 (2), pp. 120-4.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Chromosomes, Human, Pair 8*
Translocation, Genetic*
Trisomy*
Myelodysplastic Syndromes/*genetics
Aged ; Antigens, CD/biosynthesis ; DNA Probes ; Erythroid Precursor Cells/chemistry ; Erythroid Precursor Cells/ultrastructure ; Female ; Gene Library ; Glycophorins/analysis ; Granulocytes/immunology ; Granulocytes/ultrastructure ; Humans ; Immunophenotyping ; In Situ Hybridization, Fluorescence ; Male ; Megakaryocytes/ultrastructure ; Middle Aged ; Monocytes/immunology ; Monocytes/ultrastructure ; Myelodysplastic Syndromes/immunology ; Stem Cells/immunology ; Stem Cells/ultrastructure
Czasopismo naukowe
Tytuł:
Double t(1;7)(p36;p11) in a megakaryocytic crisis of chronic myelogenous leukemia with variant t(5;9;22).
Autorzy:
Hirata J; Department of Clinical Laboratory, Kyushu University Hospital, Fukuoka, Japan.
Umemura T
Nishimura J
Sadamura S
Sato H
Nawata H
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1993 Feb; Vol. 65 (2), pp. 107-10.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 22*
Chromosomes, Human, Pair 5*
Chromosomes, Human, Pair 7*
Chromosomes, Human, Pair 9*
Translocation, Genetic*
Leukemia, Myelogenous, Chronic, BCR-ABL Positive/*genetics
Chromosome Banding ; Genes, abl ; Humans ; Karyotyping ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/pathology ; Male ; Middle Aged ; Proto-Oncogenes
Czasopismo naukowe
Tytuł:
Confirmation of centromeric fusion in 7p/1q translocation associated with myelodysplastic syndrome.
Autorzy:
Hoo JJ; Office of Consolidated Laboratory Services, Rush-Presbyterian-St. Luke's Medical Center, Chicago, IL 60612.
Szego K
Jones B
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1992 Dec; Vol. 64 (2), pp. 186-8.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Centromere*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Translocation, Genetic*
Myelodysplastic Syndromes/*genetics
Adult ; Bone Marrow/pathology ; DNA Probes ; DNA, Satellite ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Lymphoma/complications ; Lymphoma/therapy ; Male ; Myelodysplastic Syndromes/complications
Czasopismo naukowe
Tytuł:
Interphase cytogenetics on paraffin sections of malignant pleural mesothelioma. A comparison to conventional karyotyping and flow cytometric studies.
Autorzy:
Tiainen M; Department of Medical Genetics, University of Helsinki, Finland.
Hopman A
Moesker O
Ramaekers F
Wessman M
Laasonen A
Pyrhönen S
Tammilehto L
Mattson K
Knuutila S
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1992 Sep; Vol. 62 (2), pp. 171-9.
Typ publikacji:
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Mesothelioma/*genetics
Pleural Neoplasms/*genetics
Flow Cytometry ; Humans ; In Situ Hybridization ; Interphase ; Karyotyping ; Paraffin Embedding
Czasopismo naukowe
Tytuł:
Survival of patients with t(1;7)(p11;p11). Report of two cases and review of the literature.
Autorzy:
Pedersen B; Danish Cancer Society, Department of Cytogenetics, Aarhus Amtssygehus.
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1992 May; Vol. 60 (1), pp. 53-9.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Translocation, Genetic*
Antineoplastic Agents/adverse effects ; Female ; Humans ; Leukemia, Myeloid, Acute/chemically induced ; Leukemia, Myeloid, Acute/genetics ; Male ; Middle Aged ; Myelodysplastic Syndromes/chemically induced ; Myelodysplastic Syndromes/genetics ; Prognosis
Czasopismo naukowe
Tytuł:
Translocation 1;7 in hematologic disorders--a report of three further cases. Absence of amplification of the gene for the epidermal growth factor receptor.
Autorzy:
Abrahamson GM; Leukaemia Research Fund Molecular and Cytogenetic Haematology Unit, John Radcliffe Hospital, Headington, Oxford, U.K.
Rack K
Buckle VJ
Oscier DG
Kelly S
Wainscoat JS
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1991 May; Vol. 53 (1), pp. 91-5.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Gene Amplification*
Translocation, Genetic*
ErbB Receptors/*genetics
Hematologic Diseases/*genetics
Aged ; Female ; Humans ; Male ; Middle Aged ; Multiple Myeloma/genetics ; Polycythemia Vera/genetics ; Primary Myelofibrosis/genetics
Czasopismo naukowe
Tytuł:
Array comparative genomic hybridization, expression array, and protein analysis of critical regions on chromosome arms 1q, 7q, and 8p in adenocarcinomas of the gastroesophageal junction.
Autorzy:
van Dekken H; Department of Pathology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands. />Tilanus HW
Hop WC
Dinjens WN
Wink JC
Vissers KJ
van Marion R
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Feb; Vol. 189 (1), pp. 37-42.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Adenocarcinoma/*genetics
Chromosomes, Human, Pair 1/*genetics
Chromosomes, Human, Pair 7/*genetics
Chromosomes, Human, Pair 8/*genetics
Esophageal Neoplasms/*genetics
Esophagogastric Junction/*metabolism
Stomach Neoplasms/*genetics
Adenocarcinoma/metabolism ; Adenocarcinoma/pathology ; Comparative Genomic Hybridization ; Esophageal Neoplasms/metabolism ; Esophageal Neoplasms/pathology ; Esophagogastric Junction/pathology ; Female ; Gene Expression Profiling ; Genome, Human ; Humans ; Male ; Middle Aged ; Neoplasm Proteins/analysis ; Neoplasm Proteins/genetics ; Oligonucleotide Array Sequence Analysis ; RNA, Messenger/metabolism ; Stomach Neoplasms/metabolism ; Stomach Neoplasms/pathology
Czasopismo naukowe
Tytuł:
Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy 7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia.
Autorzy:
Ganly P; Cancer Genetics Research Group, Christchurch School of Medicine, PO Box 4345, Christchurch, New Zealand.
McDonald M
Spearing R
Morris CM
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2004 Mar; Vol. 149 (2), pp. 125-30.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 5*
Chromosomes, Human, Pair 7*
Translocation, Genetic*
Leukemia, Myeloid, Acute/*genetics
Myelodysplastic Syndromes/*genetics
Bone Marrow Cells ; Cell Transformation, Neoplastic/genetics ; Chromosome Deletion ; Chromosome Painting ; Chromosomes, Human, Pair 1 ; Female ; Humans ; Middle Aged ; Trisomy
Czasopismo naukowe

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