Literature DB >> 13810029

The syndrome of congenital hypothyroidism with defective dehalogenation of iodotyrosines. Further observations and a discussion of the pathophysiology.

J C CHOUFOER, A A KASSENAAR, A QUERIDO.   

Abstract

Entities:  

Keywords:  HYPOTHYROIDISM/metabolism; TYROSINE/metabolism

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Year:  1960        PMID： 13810029     DOI： 10.1210/jcem-20-7-983

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN： 0021-972X            Impact factor:   5.958


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  2 in total

1.  Studies of the congenitally goitrous sheep. The iodinated compounds of serum, and circulating thyroid-stimulating hormone.

Authors:  I R Falconer
Journal:  Biochem J       Date:  1966-07       Impact factor: 3.857

2.  The Caenorhabditis elegans iodotyrosine deiodinase ortholog SUP-18 functions through a conserved channel SC-box to regulate the muscle two-pore domain potassium channel SUP-9.

Authors:  Ignacio Perez de la Cruz; Long Ma; H Robert Horvitz
Journal:  PLoS Genet       Date:  2014-02-20       Impact factor: 5.917
  2 in total

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