Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency-Reference-Cited by-同舟云学术

Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency

Published:2018-09-27 Issue:2 Volume:27 Page:216-225
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Jullien Nicolas,Romanet Pauline,Philippon Mélanie,Quentien Marie-Hélène,Beck-Peccoz Paolo,Bergada Ignacio,Odent Sylvie,Reynaud Rachel,Barlier Anne,Saveanu Alexandru,Brue Thierry,Castinetti Frederic^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/s41431-018-0264-6.pdf

Reference35 articles.

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2. Sheng HZ, Zhadanov AB, Mosinger B Jr., et al. Specification of pituitary cell lineages by the LIM homeobox gene Lhx3. Science. 1996;272:1004–7.

3. Sloop KW, Parker GE, Hanna KR, Wright HA, Rhodes SJ. LHX3 transcription factor mutations associated with combined pituitary hormone deficiency impair the activation of pituitary target genes. Gene. 2001;265:61–9.

4. Yaden BC, Savage JJ, Hunter CS, Rhodes SJ. DNA recognition properties of the LHX3b LIM homeodomain transcription factor. Mol Biol Rep. 2005;32:1–6.

5. Tian G, Singh U, Yu Y, et al. Expression and function of the LIM homeobox containing genes Lhx3 and Lhx4 in the mouse placenta. Dev Dyn. 2008;237:1517–25.

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