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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
Pokaż więcej
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

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