About: Identification of MEN1 gene mutations in families with MEN 1 and related disorders

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About: Identification of MEN1 gene mutations in families with MEN 1 and related disorders Goto Sponge Distinct Permalink

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scientific article published on October 2000

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description	videnskabelig artikel (da) article científic (ca) article scientific (oc) articol științific (ro) articolo scientifico (it) artigo científico (gl) artigo científico (pt) artigo científico (pt-br) artikull shkencor (sq) artikulong pang-agham (tl) artykuł naukowy (pl) bilimsel makale (tr) scienca artikolo (eo) teaduslik artikkel (et) tieteellinen artikkeli (fi) tudományos cikk (hu) vedecký článok (sk) vetenskaplig artikel (sv) vitenskapelig artikkel (nb) vitskapeleg artikkel (nn) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) επιστημονικό άρθρο (el) научна статия (bg) научная статья (ru) научни чланак (sr) מאמר מדעי (he) სამეცნიერო სტატია (ka) บทความทางวิทยาศาสตร์ (th) artikel ilmiah (id) bài báo khoa học (vi) naučni članak (sr-el) мақолаи илмӣ (tg-cyrl) научни чланак (sr-ec) article scientifique (fr) 2000 nî lūn-bûn (nan) 2000年の論文 (ja) 2000年論文 (zh-hk) 2000年論文 (zh-tw) 2000年論文 (zh-hant) 2000年論文 (yue) 2000年論文 (zh-mo) 2000年论文 (zh) 2000年论文 (zh-cn) 2000年论文 (zh-sg) 2000年论文 (zh-hans) 2000年论文 (wuu) 2000年论文 (zh-my) 2000년 논문 (ko) artículo científico publicado en 2000 (es) artículu científicu espublizáu en 2000 (ast) наукова стаття, опублікована в жовтні 2000 (uk) অক্টোবর ২০০০-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ (bn) scientific article published on October 2000 (en) scientific article published on October 2000 (en-ca) scientific article published on October 2000 (en-gb) مقالة علمية نشرت في أكتوبر 2000 (ar)
publication date	wds:Q36622013-79F1A667-D16E-4E5F-A983-5A035CC58FE9
publication date	2000-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q36622013-0A75F54E-1128-45B8-984C-438B3C096463
language of work or name	English
exact match	wds:Q36622013-09284449-1F96-4363-9B32-592892951723
exact match	https://scigraph.springernature.com/pub.10.1054/bjoc.2000.1380
cites work	wds:Q36622013-06BD6875-EEA4-4E47-913C-8B82196775F6 wds:Q36622013-1B989444-FC9A-4A1C-9649-89804610C946 wds:Q36622013-1EDA9FED-9655-4056-ADD5-EA48F2788568 wds:Q36622013-279F7893-3B33-45DB-BE5D-752EC5897E7C wds:Q36622013-3AE860A1-8E65-436F-84D0-387D162D8574 wds:Q36622013-3DDD5787-530C-4061-9934-82B268122094 wds:Q36622013-46822EE5-853A-4C8F-A318-570CD3B72745 wds:Q36622013-52CD42F3-41DC-46A5-A283-8F7DF53AFDEA wds:Q36622013-5E21BF44-AFD3-431A-AC4B-0B037E96C6B9 wds:Q36622013-6AFD93C1-3716-477C-B64E-E1359D8DC471 wds:Q36622013-847D7FCA-9602-4709-86D9-69F636A34A3A wds:Q36622013-851BFAFB-075C-4D28-AAA9-C45FB8B25332 wds:Q36622013-8DEA3EB3-66CD-4769-857A-368EC418E812 wds:Q36622013-A6B7F027-6AC8-46AB-A0BA-D5A358854E85 wds:Q36622013-A8A49C2E-6F2E-4C4A-ACF2-FE85EAE93D96 wds:Q36622013-D417A86E-57FC-4C25-A03C-919483E74CBB wds:Q36622013-E42E5A15-0C51-4F88-9F00-A08F304EF68D wds:Q36622013-EAA7F086-F905-476A-8800-68CE848E6522 wds:Q36622013-FF427658-0E35-431C-9752-2664EF58F535
cites work	Positional cloning of the gene for multiple endocrine neoplasia-type 1 Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1 A simple salting out procedure for extracting DNA from human nucleated cells Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states Characterization of mutations in patients with multiple endocrine neoplasia type 1. Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders Multiple facial angiofibromas and collagenomas in patients with multiple endocrine neoplasia type 1 A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors Germline mutations of the MEN1 gene in Japanese kindred with multiple endocrine neoplasia type 1. Novel V184E MEN1 germline mutation in a Japanese kindred with familial hyperparathyroidism Germline mutation of the multiple endocrine neoplasia type 1 (MEN1) gene in a family with primary hyperparathyroidism A large germline deletion of the MEN1 gene in a family with multiple endocrine neoplasia type 1.

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