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


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:
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
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
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:
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
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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:
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
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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:
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:
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:
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:
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:
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:
Complex rearrangement of chromosomes 1, 7, and 16 in chronic myelomonocytic leukemia.
Autorzy:
Fan YS
Rizkalla K
Barr RM
Pokaż więcej
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:
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:
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
Tytuł:
Chromosomal aberrations during progression of chronic myeloid leukemia identified by cytogenetic and molecular cytogenetic tools: implication of 1q12-21.
Autorzy:
Su XY; Shanghai Institute of Hematology, Rui-Jin Hospital, Shanghai Second Medical University, China.
Wong N
Cao Q
Yu LZ
Niu C
Wickham N
Johnson PJ
Chen Z
Chen SJ
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1999 Jan 01; Vol. 108 (1), pp. 6-12.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Philadelphia Chromosome*
Leukemia, Myelogenous, Chronic, BCR-ABL Positive/*genetics
Adult ; Blast Crisis ; Bone Marrow/pathology ; Child ; Chromosome Mapping ; Disease Progression ; Female ; Gene Amplification ; Humans ; Karyotyping ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/pathology ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/physiopathology ; Loss of Heterozygosity ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Addition (1)(q32) as the sole clonal chromosomal abnormality in a case of cardiac myxoma.
Autorzy:
Dobin S
Speights VO Jr
Donner LR
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1997 Jul 15; Vol. 96 (2), pp. 181-2.
Typ publikacji:
Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosome Aberrations/*genetics
Heart Neoplasms/*genetics
Myxoma/*genetics
Chromosome Banding ; Chromosome Disorders ; DNA, Neoplasm/analysis ; Female ; Humans
Opinia redakcyjna

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