Inactivating NHLH2 variants cause idiopathic hypogonadotropic hypogonadism and obesity in humans-Reference-Cited by-同舟云学术

Inactivating NHLH2 variants cause idiopathic hypogonadotropic hypogonadism and obesity in humans

Published:2022-01-23 Issue:2 Volume:141 Page:295-304
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Topaloglu A. Kemal,Simsek Enver,Kocher Matthew A.,Mammadova Jamala,Bober Ece,Kotan Leman Damla,Turan Ihsan,Celiloglu Can,Gurbuz Fatih,Yuksel Bilgin,Good Deborah J.

Funder

COBRE

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://link.springer.com/content/pdf/10.1007/s00439-021-02422-9.pdf

Reference43 articles.

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3. Al Rayyan N, Wankhade UD, Bush K, Good DJ (2013) Two single nucleotide polymorphisms in the human nescient helix-loop-helix 2 (NHLH2) gene reduce mRNA stability and DNA binding. Gene 512:134–142. https://doi.org/10.1016/j.gene.2012.09.068

4. Al Rayyan N, Zhang J, Burnside AS, Good DJ (2014) Leptin signaling regulates hypothalamic expression of nescient helix-loop-helix 2 (Nhlh2) through signal transducer and activator 3 (Stat3). Mol Cell Endocrinol 384:134–142. https://doi.org/10.1016/j.mce.2014.01.017

5. Bianco SD, Kaiser UB (2009) The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism. Nat Rev Endocrinol 5:569–576. https://doi.org/10.1038/nrendo.2009.177

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