About: Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism

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About: Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 1998 (uk) im August 1998 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q58862086-AB1BC96B-C55E-4A99-8248-F42A17D02126
publication date	1998-08-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58862086-5B104D1F-18AE-4688-B924-D013FBF47618
language of work or name	English
author name string	wds:Q58862086-053E6CF1-9AFB-495A-B34F-7657C878982F wds:Q58862086-0E9B558B-E8E8-4652-9EC2-C9807F334B4B wds:Q58862086-15AF79A5-AA60-43FD-BAA8-73A7A1783DAF wds:Q58862086-173FD848-2CAB-4AFB-BC2C-F8A0BB0167B5 wds:Q58862086-20E03523-5841-429A-A3A9-7F2832E40966 wds:Q58862086-27B02F7F-B4AE-4B39-9B11-654CF3350197 wds:Q58862086-2900FABA-C0F6-49E3-872A-4BB6D5924807 wds:Q58862086-2EE01D20-29B3-4FBA-A05F-F10491873410 wds:Q58862086-2FA750CC-33DE-4886-B96B-B1C5DA1F1919 wds:Q58862086-5075EFCD-E547-437B-9B1A-DDE9DFDCCF5D wds:Q58862086-54C361B6-91E2-494A-B113-00346E6FA176 wds:Q58862086-55FFD933-B462-4204-9614-6BDE8161A03B wds:Q58862086-76CFF34D-00F6-45FA-873A-43BEBD77F9B0 wds:Q58862086-79751EAB-CF2A-49D3-AD6F-9CCD67583345 wds:Q58862086-7F736A28-FC84-4E04-9B2A-A005C8535B1D wds:Q58862086-86A5A371-F0A2-4C82-9969-76F7EF639308 wds:Q58862086-8A1F518E-EC0F-4D3F-8848-8A0476F56596 wds:Q58862086-9D4ECD97-C3DF-421F-8339-F7A67AEC3A51 wds:Q58862086-A951238C-BD36-411F-9055-240291478FFA wds:Q58862086-C257BE86-8860-41D5-B2EB-90F24237D2ED wds:Q58862086-C93EF1F5-C4D3-4AD0-A6B3-6EF5A2566488 wds:Q58862086-D2885B1A-C714-4BF7-B716-AB0FAE7CC2DB
author name string	Stewart C Farnebo F Larsson C Skogseid B Walters M Weber G Epstein M Tranebjaerg L Alford F Parente F Khodaei S Kytölä S Hayward N Silins G Beckers A Jorde R Cardinal J Hurley D Salmela P Wong FK Bergman L Phelan C
rdfs:label	Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism (en) Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism (nl)
skos:prefLabel	Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism (en) Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism (nl)
name	Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism (en) Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism (nl)
author	wds:Q58862086-0AD11F71-0014-426B-B792-04385BCBD880 wds:Q58862086-C1FA1604-FB28-4FB7-85E5-F08AA197732A wds:Q58862086-FF0FAB14-806A-4C3E-9604-20BF7E6DB2F7
author	Bin Tean Teh Sean Grimmond Matthew Edwards
title	wds:Q58862086-889CA933-2C74-474F-8920-3C60496E57E2
title	Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism (en)
page(s)	wds:Q58862086-0F05DD22-546A-4AED-AE7A-51C079DE0DE9
page(s)	2621-2626
instance of	wds:Q58862086-C56F84A7-F3FC-49FE-A035-5B280372A0EE
instance of	scholarly article
main subject	wds:Q58862086-39EA9021-2DE2-4A2F-BBEE-A75FB2C39263 wds:Q58862086-44B107D5-17C3-4730-9DDA-5287B172093B wds:Q58862086-D15D2307-507D-437B-B4DA-7743894F24A5
main subject	multiple endocrine neoplasia type 1 hyperparathyroidism multiple endocrine neoplasia
PubMed ID	wds:Q58862086-674EAA93-5C68-4770-983B-382C147C9476
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9709921
PubMed ID	9709921
published in	wds:Q58862086-E0599B2E-3454-478C-AE90-728053FDA807
published in	The Journal of Clinical Endocrinology and Metabolism
issue	wds:Q58862086-F421A3DA-AC90-451D-9FE1-061A0128D6B0
volume	wds:Q58862086-79BCCDDE-EFC5-45F6-A96B-701F40C2EE1F
issue	8
volume	83
DOI	wds:Q58862086-70C74453-4779-4B9D-8F82-08334E83E902
DOI	http://dx.doi.org/10.1210/JCEM.83.8.5059
DOI	10.1210/JCEM.83.8.5059
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58862086
is cites work of	Acromegaly HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours Identification and characterization of JunD missense mutants that lack menin binding Stable overexpression of MEN1 suppresses tumorigenicity of RAS. Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology Molecular pathogenesis of acromegaly Familial isolated pituitary adenomas (FIPA) and the pituitary adenoma predisposition due to mutations in the aryl hydrocarbon receptor interacting protein (AIP) gene Multiple endocrine neoplasia type 1 Identification of MEN1 gene mutations in families with MEN 1 and related disorders

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