The human HNP36 gene is localized to chromosome 11q13 and produces alternative transcripts that are not mutated in multiple endocrine neoplasia, type 1 (MEN I) syndrome
- Author
- WILLIAMS, J. B1 ; REXER, B1 ; GERHARD, D. S4 ; SIRRIPURAPU, S1 ; JOHN, S1 ; GOLDSTEIN, R1 2 ; PHILLIPS, J. A1 ; HALEY, L. L3 ; SAIT, S. N. J3 ; SHOWS, T. B3 ; SMITH, C. M4
[1] Department of Medicine, Department of Biochemistry, and the Vanderbilt Cancer Center, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, United States
[2] Department of Veteran Affairs Medical Center, Nashville, Tennessee 37212, United States
[3] Department of Human Genetics, Roswell Park Cancer Center, Buffalo, New York 14263, United States
[4] Department of Genetics, Washington University School of Medicine, St. Louis, Missouri 63110, United States - Source
Genomics (San Diego, Calif.). 1997, Vol 42, Num 2, pp 325-330 ; ref : 1 p.1/4
- ISSN
- 0888-7543
- Scientific domain
- Cell biology, histology; Genetics
- Publisher
- Elsevier, San Diego, CA
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Carte génétique Chromosome C11 Expression génique Homme Homologie Hypophyse Mutation Organisation gène Parathyroïde Polyadénomatose endocrinienne I Région critique Séquence nucléotide Tumeur Gène HNP36 Biologie moléculaire Endocrinopathie Maladie héréditaire Tumeur bénigne
- Keyword (en)
- Genetic mapping Chromosome C11 Gene expression Human Homology Pituitary gland Mutation Gene organization Parathyroid glands Multiple endocrine neoplasia type I Critical region Nucleotide sequence Tumor Molecular biology Endocrinopathy Genetic disease Benign neoplasm
- Keyword (es)
- Mapa genético Cromosoma C11 Expresión genética Hombre Homología Hipófisis Mutación Organización gene Paratiroides Neoplasia endocrina múltiple tipo I Región crítica Secuencia nucleótido Tumor Biología molecular Endocrinopatía Enfermedad hereditaria Tumor benigno
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B21 Endocrinopathies / 002B21C Thyroid. Thyroid axis (diseases) / 002B21C02 Malignant tumors
- Discipline
- Endocrinopathies
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 2719013
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
10.1006/geno.1997.4751 
https://dx.doi.org/10.1006/geno.1997.4751
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