Absence of germline mutations in exons 5-9 of the p53 gene in patients with Li-Fraumeni-like (SBLA) and familial adenomatous polyposis heritable cancer syndromes
- Author
- MOORE, S. K1 ; ZAMBRANO, N2 ; LYNCH, H. T3 4 ; LIPKIN, M5 ; KOPELOVICH, L6 7
[1] Food and Drug Administration, Center for Drug Evaluation and Research, Division of Metabolism and Endocrine Drug Products, Rockville, Maryland, United States
[2] National Institutes of Health, National Cancer Institute, Laboratory of Cell Biology, Bethesda, Maryland, United States
[3] M. Department of Preventative Medicine, Omaha, Nebraska, United States
[4] The Creighton Cancer Center, Omaha, Nebraska, United States
[5] Gastrointestinal Research, Memorial Sloan Kettering Cancer Center, New York, New York, United States
[6] Department of Pathology and Department of Molecular Biology, University of South Florida College of Medicine, Tampa, United States
[7] Veterans Administration Medical Center, Bay Pines, Florida, United States - Source
Cancer genetics and cytogenetics. 1996, Vol 90, Num 2, pp 125-129 ; ref : 44 ref
- CODEN
- CGCYDF
- ISSN
- 0165-4608
- Scientific domain
- Medical oncology; Genetics
- Publisher
- Elsevier Science, New York, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Culture cellulaire DNA Déterminisme génétique Exploration Fibroblaste Gène suppresseur tumeur Homme Lignée germinale Mutation Polymorphisme conformation simple brin Polypose rectocolique familiale Séquence nucléotide Gène p53 Li Fraumeni like syndrome Appareil digestif pathologie Génétique Intestin pathologie Maladie héréditaire Tumeur maligne
- Keyword (en)
- Cell culture DNA Genetic inheritance Exploration Fibroblast Tumor suppressor gene Human Germ line Mutation Single strand conformation polymorphism Familial adenomatous polyposis coli Nucleotide sequence p53 gene Li Fraumeni like syndrome Digestive diseases Genetics Intestinal disease Genetic disease Malignant tumor
- Keyword (es)
- Cultivo celular DNA Determinismo genético Exploración Fibroblasto Gen supresor tumor Hombre Línea germinal Mutación Polimorfismo conformación cadena única Poliadenoma del intestino grueso Secuencia nucleótido Aparato digestivo patología Genética Intestino patología Enfermedad hereditaria Tumor maligno
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B04 Tumors / 002B04C Multiple tumors. Solid tumors. Tumors in childhood (general aspects)
- Discipline
- Tumours
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3234589
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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DOI
10.1016/S0165-4608(96)00072-6 
https://dx.doi.org/10.1016/S0165-4608(96)00072-6
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