Literature DB >> 10966852

Multiple endocrine neoplasia type 1.

F Ki Wong1, J Burgess, M Nordenskjöld, C Larsson, B Tean Teh.   

Abstract

The recent cloning of the gene responsible for multiple endocrine neoplasia type 1 (MEN 1) has opened new avenues for both clinical and basic science research in the field of endocrine oncology. A large amount of genetic information, particularly those in relation to germline and somatic mutations, has since been published during the last 2 years. This new knowledge has provided important insights into its gene function. The significance of these advances in relation to clinical management and future directions for research is discussed. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10966852     DOI: 10.1006/scbi.2000.0150

Source DB:  PubMed          Journal:  Semin Cancer Biol        ISSN: 1044-579X            Impact factor:   15.707


  2 in total

1.  Management of pancreatic endocrine tumors in multiple endocrine neoplasia type 1.

Authors:  Maria A Kouvaraki; Suzanne E Shapiro; Gilbert J Cote; Jeffrey E Lee; James C Yao; Steven G Waguespack; Robert F Gagel; Douglas B Evans; Nancy D Perrier
Journal:  World J Surg       Date:  2006-05       Impact factor: 3.352

2.  Conditional inactivation of the MEN1 gene leads to pancreatic and pituitary tumorigenesis but does not affect normal development of these tissues.

Authors:  Christine A Biondi; Michael G Gartside; Paul Waring; Kelly A Loffler; Mitchell S Stark; Mark A Magnuson; Graham F Kay; Nicholas K Hayward
Journal:  Mol Cell Biol       Date:  2004-04       Impact factor: 4.272

  2 in total

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