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Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk

Author
YANG, Rongxi3 ; BOWANG CHEN5 ; MEINDL, Alfons13 ; BARTRAM, Claus R2 ; SCHMUTZLER, Rita K7 8 ; BURWINKEL, Barbara1 3 ; HEMMINKI, Kari5 6 ; WAPPENSCHMIDT, Barbara7 8 ; ENGEL, Christoph9 ; SUTTER, Christian2 ; DITSCH, Nina4 ; WEBER, Bernhard H. F10 ; NIEDERACHER, Dieter11 ; ARNOLD, Norbert12
[1] Helmholtz-University Group Molecular Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 581, 69120 Heidelberg, Germany
[2] Institute of Human Genetics, University of Heidelberg, 69120 Heidelberg, Germany
[3] Division Molecular Biology of Breast Cancer, Department of Gynecology and Obstetrics, University of Heidelberg, 69120 Heidelberg, Germany
[4] Department for Obstetrics and Gynaecology, Ludwig Maximilians Universität, Marchionini Str. 15, 81377 Munich, Germany
[5] Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, 69120 Heidelberg, Germany
[6] Department of Biosciences at Novum, Karolinska Institute, 14157 Huddinge, Sweden
[7] Division of Molecular Gynaeco-Oncology, Department of Gynaecology and Obstetrics, Clinical Center University of Cologne, 50931 Köln, Germany
[8] Center of Molecular Medicine Cologne (CMMC), University Hospital of Cologne, 50931 Köln, Germany
[9] Department of Medical Informatics, Statistics and Epidemiology, University of Leipzig, 04107 Leipzig, Germany
[10] Institute of Human Genetics, University of Regensburg, 93053 Regensburg, Germany
[11] Division of Molecular Genetics, Department of Gynaecology and Obstetrics, Clinical Center University of Diisseldorf, 40225 Düsseldorf, Germany
[12] Division of Oncology, Department of Gynaecology and Obstetrics, University Hospital Schleswig-Holstein, 24105 Kiel, Germany
[13] Department of Gynaecology and Obstetrics, Klinikum rechts der Isar, Technical University of Munich, 81675 Munich, Germany
Source

Breast cancer research and treatment. 2009, Vol 118, Num 2, pp 407-413, 7 p ; ref : 50 ref

CODEN
BCTRD6
ISSN
0167-6806
Scientific domain
Medical oncology; Obstetrics, gynecology, andrology; Pharmacology drugs
Publisher
Springer, Dordrecht
Publication country
Netherlands
Document type
Article
Language
English
Author keyword
BRCA1 BRCA2 Breast cancer risk Case―control study Codon-usage
Keyword (fr)
Analyse Cancer du sein Cancer familial Codon Etude cas témoin Facteur risque Gène BRCA1 Gène BRCA2 Gène suppresseur tumeur Génotype Homme Polymorphisme Variabilité génétique Cancer Pathologie de la glande mammaire Pathologie du sein Tumeur maligne
Keyword (en)
Analysis Breast cancer Familial cancer Codon Case control study Risk factor BRCA1 gene BRCA2 gene Tumor suppressor gene Genotype Human Polymorphism Genetic variability Cancer Mammary gland diseases Breast disease Malignant tumor
Keyword (es)
Análisis Cáncer del pecho Cáncer familiar Codón Estudio caso control Factor riesgo Gen BRCA1 Gen BRCA2 Gen supresor tumor Genotipo Hombre Polimorfismo Variabilidad genética Cáncer Glándula mamaria patología Seno patología Tumor maligno
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B20 Gynecology. Andrology. Obstetrics / 002B20E Mammary gland diseases / 002B20E02 Tumors

Discipline
Gynecology. Andrology. Obstetrics
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
22109154

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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