The ambiguous role of NKX2-5 mutations in thyroid dysgenesis.

van Engelen, Klaartje; Mommersteeg, Mathilda T M; Baars, Marieke J H; Lam, Jan; Ilgun, Aho; van Trotsenburg, A S Paul; Smets, Anne M J B; Christoffels, Vincent M; Mulder, Barbara J M; Postma, Alex V

van Engelen, Klaartje; Mommersteeg, Mathilda T M; Baars, Marieke J H; Lam, Jan; Ilgun, Aho; van Trotsenburg, A S Paul; Smets, Anne M J B; Christoffels, Vincent M; Mulder, Barbara J M; Postma, Alex V.

Affiliation

van Engelen K; Department of Cardiology, Academic Medical Center, Amsterdam, The Netherlands. k.vanengelen@amc.uva.nl

PLoS One ; 7(12): e52685, 2012.

Article in En | MEDLINE | ID: mdl-23285148

Subject(s)

Homeodomain Proteins/genetics; Mutation; Thyroid Dysgenesis/genetics; Transcription Factors/genetics; Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Sequence; Animals; Cell Nucleus/metabolism; Child; DNA-Binding Proteins/genetics; DNA-Binding Proteins/metabolism; Female; Homeobox Protein Nkx-2.5; Homeodomain Proteins/metabolism; Humans; Male; Middle Aged; Pedigree; Phenotype; Promoter Regions, Genetic; Protein Transport; Sequence Alignment; Transcription Factors/metabolism; Transcriptional Activation; Young Adult

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Homeodomain Proteins / Thyroid Dysgenesis / Mutation Type of study: Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Animals / Child / Female / Humans / Male / Middle aged Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2012 Type: Article Affiliation country: Netherlands

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