A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
- Author
- HEMMINKI, A1 ; MARKIE, D2 ; JÄRVINEN, H6 ; KRISTO, P1 ; PELIN, K1 5 ; RIDANPÄÄ, M1 5 ; SALOVAARA, R1 7 ; TORO, T2 ; BODMER, W8 ; OLSCHWANG, S9 ; OLSEN, A. S10 ; STRATTON, M. R3 ; TOMLINSON, I3 4 ; DE LA CHAPELLE, A1 11 ; AALTONEN, L. A1 ; AVIZIENYTE, E1 ; ROTH, S1 ; LOUKOLA, A1 ; BIGNELL, G3 ; WARREN, W3 ; AMINOFF, M1 5 ; HÖGLUND, P1
[1] Department of Medical Genetics, Haartman Institute, PO Box 21 (Haartmaninkatu 3), University of Helsinki, 00014, Finland
[2] Department of Pathology, Dunedin School of Medicine, PO Box 913, Dunedin, New Zealand
[3] Section of Cancer Genetics, Haddow Laboratories, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, United Kingdom
[4] Nuffield Department of Clinical Medicine, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom
[5] Folkhälsan Institute of Genetics, Mannerheimintie 97, 00280 Helsinki, Finland
[6] Second Department of Surgery, Helskinki University Central Hospital, Haartmaninkatu 4, 00290 Helsinki, Finland
[7] Department of Pathology, Haartman Institute, PO Box 21 (Haartmaninkatu 3), University of Helsinki, 00014, Finland
[8] ICRF Cancer and Immunogenetics Laboratory, Institute of Molecular Medicine, John Radcliffe Hospital, Oxford OX3 9DS, United Kingdom
[9] Inserm U434, Fondation Jean Dausset-CEPH, 75010 Paris, France
[10] Human Genome Center, L-452, Lawrence Livermore National Laboratory, Livermore, California 94550, United States
[11] Comprehensive Cancer Center, Ohio State University, 420 W 12th Avenue, Columbus, Ohio 43210, United States - Source
Nature (London). 1998, Vol 391, Num 6663, pp 184-187 ; ref : 15 ref
- CODEN
- NATUAS
- ISSN
- 0028-0836
- Scientific domain
- Multidisciplinary
- Publisher
- Nature Publishing, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aberration chromosomique Analyse structurale Chromosome F19 Homme Maladie héréditaire Marqueur génétique Mutation Peutz Jeghers syndrome Protein kinase Séquence aminoacide Séquence nucléotide Appareil digestif pathologie Enzyme Lentiginose Peau pathologie Polypose Transferases Tumeur bénigne
- Keyword (en)
- Chromosomal aberration Structural analysis Chromosome F19 Human Genetic disease Genetic marker Mutation Peutz Jeghers syndrome Protein kinase Aminoacid sequence Nucleotide sequence Digestive diseases Enzyme Lentiginosis Skin disease Polyposis Transferases Benign neoplasm
- Keyword (es)
- Aberración cromosómica Análisis estructural Cromosoma F19 Hombre Enfermedad hereditaria Marcador genético Mutación Peutz Jeghers síndrome Protein kinase Secuencia aminoácido Secuencia nucleótido Aparato digestivo patología Enzima Lentiginosis Piel patología Poliposis Transferases Tumor benigno
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B13 Gastroenterology. Liver. Pancreas. Abdomen / 002B13B Stomach. Duodenum. Small intestine. Colon. Rectum. Anus / 002B13B01 Tumors
- Discipline
- Gastroenterology. Liver. Pancreas. Abdomen
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 2103287
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
10.1038/34432 
https://dx.doi.org/10.1038/34432
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