About: Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis

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About: Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis Goto Sponge NotDistinct Permalink

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scientific journal article

Attributes	Values
rdf:type	Item
description	artículu científicu espublizáu en 2010 (ast) vědecký článek publikovaný v roce 2010 (cs) article scientifique publié en 2010 (fr) наукова стаття, опублікована в лютому 2010 (uk) 2010 թվականի փետրվարին հրատարակված գիտական հոդված (hy) 2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած (hyw) مقالة علمية (نشرت في فبراير 2010) (ar) vedecký článok (publikovaný 2010/02/01) (sk) wetenschappelijk artikel (gepubliceerd op 2010/02/01) (nl) im Februar 2010 veröffentlichter wissenschaftlicher Artikel (de) scientific journal article (en)
publication date	wds:Q28116269-A0B7B053-04A4-44AB-81B9-0D78D72BD36C
publication date	2010-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28116269-97EC4B3D-39EF-489D-80E5-5EE22ED99A95
language of work or name	English
exact match	wds:Q28116269-173A715C-2C3F-4943-B994-86C34E55EB88
exact match	https://scigraph.springernature.com/pub.10.1007/s10528-009-9306-7
cites work	wds:Q28116269-8D61081B-E6E6-4ABC-A0E8-849AA406351D wds:Q28116269-FDF4AD6F-7855-4305-840A-59170A1AF22E
cites work	Thyroid-specific gene expression Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency
author name string	wds:Q28116269-12AB08CD-F66C-4574-BF84-2493E60D4CF8 wds:Q28116269-7D5FC497-8D19-46DA-961E-619480A2BA4A wds:Q28116269-B1209EF3-DBA2-4978-97C1-78A85C92A9D7 wds:Q28116269-E138EA42-74C3-4ECE-A9B7-C97FB0C8EDDD
author name string	Fatimah Harun In-Nee Kang Maslinda Musa Sarni Mat Junit
rdfs:label	Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis (en) Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis (nl) Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis (ast)
skos:prefLabel	Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis (en) Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis (nl) Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis (ast)
name	Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis (en) Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis (nl) Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis (ast)
title	wds:Q28116269-56C15E27-1AEF-4C2A-9B21-EF4F738BB1E9
title	Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis (en)
page(s)	wds:Q28116269-91ED22F3-C00C-48A6-B0F4-3EE1BFD20B13
page(s)	141–151
instance of	wds:Q28116269-EF0426B6-A558-4A6E-AB95-9FAE99C17B82
instance of	scholarly article
main subject	wds:Q28116269-032BF24B-1773-44B0-A9B6-7525B4CE096D wds:Q28116269-1A72B90E-399F-4A6E-B56D-955223B0E793 wds:Q28116269-4744D99E-8EE4-4F38-B94B-7E212DD4D087 wds:Q28116269-7CFA0534-ADEA-445C-A001-C97B0334C1B3 wds:Q28116269-DEAED329-B82C-4DB1-9B59-BFF0ACC4E2EF
main subject	Malaysia thyroid dysgenesis congenital hypothyroidism Forkhead box E1 sequence-specific DNA binding
PubMed ID	wds:Q28116269-C0ABF83D-16DA-4F6D-8F24-EF1D6CB7EAEA
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/20094846
PubMed ID	20094846
published in	wds:Q28116269-999AF5D6-1C32-43F7-869B-027BD00ADF51
published in	Biochemical Genetics
issue	wds:Q28116269-3CA73214-A126-46FC-AB18-92E9E6D449A6
volume	wds:Q28116269-D114D0DC-34C4-407A-82D7-37B1DCAAE99F
issue	1-2
volume	48
DOI	wds:Q28116269-D0AEBFA8-0794-49C6-83C0-92DF89B4A035
DOI	http://dx.doi.org/10.1007/S10528-009-9306-7
DOI	10.1007/S10528-009-9306-7
ResearchGate publication ID	wds:Q28116269-A961331F-C0E1-4670-9FDC-A0AB1427A23D
ResearchGate publication ID	41112919
Dimensions Publication ID	wds:Q28116269-FDFD9E5B-7CF3-4278-978D-E2A359768B3A
Dimensions Publication ID	1019417301
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28116269
is cites work of	A novel FOXE1 mutation (R73S) in Bamforth-Lazarus syndrome causing increased thyroidal gene expression The molecular causes of thyroid dysgenesis: a systematic review Functional analyses of C.2268dup in thyroid peroxidase gene associated with goitrous congenital hypothyroidism Neurocristopathies: New insights 150 years after the neural crest discovery
is cites work of	wds:Q37686783-D8598E81-7EC4-4CD8-AFCE-F45AF81723DA wds:Q38108710-379B0DB5-6ED0-4189-82CF-DB8D9061CFAD wds:Q28115316-80834532-3BED-46B2-820F-E228426ED1C5 wds:Q88869535-574BB313-6320-4E26-8250-33F602809A75
is pr:P248 of	wdref:52990bd02cf62ebd3a1c89c3415cfae2d99c8e34 wdref:8d153f44fadae01f8d7c8e6426e8b5aa6c11c1b9

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