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[Multiple endocrine neoplasia 1 (MEN 1)].
Nihon Rinsho. 2000 Jul; 58(7):1434-6.NR

Abstract

Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominant familial cancer syndrome characterized by tumors in parathyroids, enteropancreatic endocrine tissues, and anterior pituitary. In 1997, the MEN 1 gene was identified and cloned. It is on chromosome 11q13 and has 10 exons. It encodes a 610 amino acid protein called MENIN. However, many different germline mutations in MEN 1 families have reported, there were no hotspot of mutation. The correlation between MEN 1 mutation and clinical datas has not been established yet. Recently, the possible function of MENIN protein has reported. The identification of MEN 1 mutation by employing DNA test, will facilitate early diagnosis and treatment.

Authors+Show Affiliations

Division of Diagnostic Pathology, Keio University Hospital.No affiliation info available

Pub Type(s)

English Abstract
Journal Article
Review

Language

jpn

PubMed ID

10921319

Citation

Kameyama, K, and H Takami. "[Multiple Endocrine Neoplasia 1 (MEN 1)]." Nihon Rinsho. Japanese Journal of Clinical Medicine, vol. 58, no. 7, 2000, pp. 1434-6.
Kameyama K, Takami H. [Multiple endocrine neoplasia 1 (MEN 1)]. Nihon Rinsho. 2000;58(7):1434-6.
Kameyama, K., & Takami, H. (2000). [Multiple endocrine neoplasia 1 (MEN 1)]. Nihon Rinsho. Japanese Journal of Clinical Medicine, 58(7), 1434-6.
Kameyama K, Takami H. [Multiple Endocrine Neoplasia 1 (MEN 1)]. Nihon Rinsho. 2000;58(7):1434-6. PubMed PMID: 10921319.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Multiple endocrine neoplasia 1 (MEN 1)]. AU - Kameyama,K, AU - Takami,H, PY - 2000/8/2/pubmed PY - 2000/10/21/medline PY - 2000/8/2/entrez SP - 1434 EP - 6 JF - Nihon rinsho. Japanese journal of clinical medicine JO - Nihon Rinsho VL - 58 IS - 7 N2 - Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominant familial cancer syndrome characterized by tumors in parathyroids, enteropancreatic endocrine tissues, and anterior pituitary. In 1997, the MEN 1 gene was identified and cloned. It is on chromosome 11q13 and has 10 exons. It encodes a 610 amino acid protein called MENIN. However, many different germline mutations in MEN 1 families have reported, there were no hotspot of mutation. The correlation between MEN 1 mutation and clinical datas has not been established yet. Recently, the possible function of MENIN protein has reported. The identification of MEN 1 mutation by employing DNA test, will facilitate early diagnosis and treatment. SN - 0047-1852 UR - https://www.unboundmedicine.com/medline/citation/10921319/[Multiple_endocrine_neoplasia_1__MEN_1_]_ L2 - http://www.diseaseinfosearch.org/result/4954 DB - PRIME DP - Unbound Medicine ER -