About: A mouse model demonstrates a multigenic origin of congenital hypothyroidism

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scientific journal article

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rdf:type	Item
description	article scientifique publié en 2005 (fr) artículu científicu espublizáu en 2005 (ast) vědecký článek publikovaný v roce 2005 (cs) مقالة علمية (نشرت في ديسمبر 2005) (ar) 2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված (hy) 2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в грудні 2005 (uk) wetenschappelijk artikel (gepubliceerd op 2005/12/01) (nl) vedecký článok (publikovaný 2005/12/01) (sk) scientific journal article (en) im Dezember 2005 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28592837-362C8D1D-8E08-4DEE-89AA-61FACFC24A8E
publication date	2005-09-08 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28592837-28C83043-ABEA-4A0C-821E-D062F5825423
language of work or name	English
author name string	wds:Q28592837-0083C606-91E4-4D1A-B809-0DBE784AF3F3 wds:Q28592837-0C8A46F2-CFEF-43C9-A5E6-3C17EDFEA4C9 wds:Q28592837-31FF25ED-2C6C-4E14-BF01-4F34F1C325C5 wds:Q28592837-64D4C30E-BBF1-485D-A092-2444C7279A99 wds:Q28592837-67584A92-0441-4E8E-9017-4C49C79D578D wds:Q28592837-8102FB39-A729-478B-99E4-A96C6581705D wds:Q28592837-8F834E2E-C8A5-4E8C-A8B5-76E80FF8C86C wds:Q28592837-B27B0C14-1F0D-40DE-AD54-0CF0B0F591DC wds:Q28592837-B73C1ED7-2140-4E75-9BEE-81E2EE7C0086 wds:Q28592837-BA48E999-D445-453B-82D9-86D7BC28EE92 wds:Q28592837-BB024D3A-2584-4987-B7EE-D698E95E7E41
OpenCitations bibliographic resource ID	wds:Q28592837-56C48330-0777-45C8-83AC-6D49AC1ED8D1
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/2256355
author name string	Shioko Kimura Mario De Felice Ahmed Mansouri Gennaro Chiappetta Andrea Affuso Annamaria Rosica Roberto Di Lauro Elena Amendola Daniela Terracciano Vincenzo Macchia Paolo Emidio Macchia
OpenCitations bibliographic resource ID	2256355
rdfs:label	A mouse model demonstrates a multigenic origin of congenital hypothyroidism (en) A mouse model demonstrates a multigenic origin of congenital hypothyroidism (nl) A mouse model demonstrates a multigenic origin of congenital hypothyroidism (ast)
skos:prefLabel	A mouse model demonstrates a multigenic origin of congenital hypothyroidism (en) A mouse model demonstrates a multigenic origin of congenital hypothyroidism (nl) A mouse model demonstrates a multigenic origin of congenital hypothyroidism (ast)
name	A mouse model demonstrates a multigenic origin of congenital hypothyroidism (en) A mouse model demonstrates a multigenic origin of congenital hypothyroidism (nl) A mouse model demonstrates a multigenic origin of congenital hypothyroidism (ast)
author	wds:Q28592837-78DEDDAF-CF48-4E2D-8AA1-8E65875D9424 wds:Q28592837-B9367422-F9A0-46AF-8B50-1E7D38062F24
author	Claudio Arra Pasquale De Luca
title	wds:Q28592837-B6E35CD6-1D4B-4283-A45E-22EC6DD7B0AF
title	A mouse model demonstrates a multigenic origin of congenital hypothyroidism (en)
page(s)	wds:Q28592837-B4574D14-5D71-4464-835D-7B7D830BED45
page(s)	5038-5047
instance of	wds:Q28592837-EFAA2F63-5E47-480D-8C17-EE506E589AC4
instance of	scholarly article
main subject	wds:Q28592837-1BD3E587-F973-4A4F-9C06-A297FAA2764B wds:Q28592837-F59B8A06-98D0-4D3C-81EF-348D18AF6CE0
main subject	congenital hypothyroidism NK2 homeobox 1
PubMed ID	wds:Q28592837-9377A957-C744-4C8C-869E-D2E1D7657E33
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16150900
PubMed ID	16150900
published in	wds:Q28592837-0BEFF694-047F-4958-A762-78025C56526F
published in	Endocrinology
issue	wds:Q28592837-477FC902-D0A5-4380-B8B5-31020104EF86
volume	wds:Q28592837-07F922A0-ED06-4F47-B3EE-96136E6170D5
issue	12
volume	146
DOI	wds:Q28592837-8FDA6C9D-251A-4E10-A2DA-6434B70C7F06
DOI	http://dx.doi.org/10.1210/EN.2005-0882
DOI	10.1210/EN.2005-0882
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28592837
is cites work of	Deletion of the RNaseIII enzyme dicer in thyroid follicular cells causes hypothyroidism with signs of neoplastic alterations Thyroid transcription factors in development, differentiation and disease The microRNA-processing enzyme Dicer is essential for thyroid function The molecular causes of thyroid dysgenesis: a systematic review Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ. Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis Variation by ethnicity in the prevalence of congenital hypothyroidism due to thyroid dysgenesis Abnormal motor phenotype at adult stages in mice lacking type 2 deiodinase In vivo role of different domains and of phosphorylation in the transcription factor Nkx2-1. Microarray technology--advances, applications, future prospects Next generation sequencing in endocrine practice Genetic analysis of the PAX8 gene in children with congenital hypothyroidism and dysgenetic or eutopic thyroid glands: identification of a novel sequence variant A frequent oligogenic involvement in congenital hypothyroidism. Fate map of serotonin transporter-expressing cells in developing mouse thyroid. Hypothalamus-Pituitary-Thyroid Axis. OligoPVP: Phenotype-driven analysis of individual genomic information to prioritize oligogenic disease variants WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion. Loss of HCN2 leads to delayed gastrointestinal motility and reduced energy intake in mice. Genetic background and window of exposure contribute to thyroid dysfunction promoted by low-dose exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin in mice Double knock-out of Hmga1 and Hipk2 genes causes perinatal death associated to respiratory distress and thyroid abnormalities in mice New insight into ectopic thyroid glands between the neck and maxillofacial region from a 42-case study Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure

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