The gene for multiple endocrine neoplasia type 1: recent findings-Reference-Cited by-同舟云学术

The gene for multiple endocrine neoplasia type 1: recent findings

Published:1999-07 Issue:1 Volume:25 Page:119-122
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Marx S.J,Agarwal S.K,Heppner C,Kim Y.S,Kester M.B,Goldsmith P.K,Skarulis M.C,Spiegel A.M,Burns A.L,Debelenko L.V,Zhuang Z,Lubensky I.A,Liotta L.A,Emmert-Buck M.R,Guru S.C,Manickam P,Crabtree J.S,Collins F.S,Chandrasekharappa S.C

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference40 articles.

1. a. Agarwal, S. K., Debelenko, L. V., Kester, M. B., et al. Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families. Hum Mut 12:75–82; 1998. b. Agarwal, S. K., Guru, J. C., Heppner, C., et al. Menin interacts with the API transcription factor junD and represses junD-activated transcription. Cell 96:143–152; 1999.

2. Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states;Agarwal;Hum Mol Genet,1997

3. Comparative genome hybridization analysis of human parathyroid tumors;Agarwal;Cancer Genet Cytogen,1998

4. Somatic mutations of the MEN1 tumor suppressor gene detected in sporadic angiofibromas;Boni;J Invest Dermatol,1998

5. Aggressive forms of gastric neuroendocrine tumors in multiple endocrine neoplasia type 1;Bordi;Am J Surg Pathol,1997

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