Copy number variants of Ras/MAPK pathway genes in patients with isolated cryptorchidism-Reference-Cited by-同舟云学术

Copy number variants of Ras/MAPK pathway genes in patients with isolated cryptorchidism

Published:2017-07-10 Issue:5 Volume:5 Page:923-930
ISSN:2047-2919
Container-title:Andrology
language:en
Short-container-title:

Author:

Rodríguez F.¹^ORCID,Vallejos C.¹,Giraudo F.¹,Unanue N.¹,Hernández M. I.¹,Godoy P.²,Célis S.³,Martín-Arenas R.⁴,Palomares-Bralo M.⁴,Heath K. E.⁴,López M. T.³,Cassorla F.¹

Affiliation:

1. Institute of Maternal and Child Research; School of Medicine; University of Chile; Santiago Chile

2. Pediatric Service; Hospital Base San José; Osorno Chile

3. Pediatric Urology Department; Hospital Clínico San Borja - Arriarán; Santiago Chile

4. Institute of Medical and Molecular Genetics (INGEMM); Hospital Universitario La Paz, IdiPAZ, UAM and CIBERER, ISCIII; Madrid Spain

Funder

Fondo Nacional de Desarrollo Científico y Tecnológico

Publisher

Wiley

Subject

Urology,Endocrinology,Reproductive Medicine,Endocrinology, Diabetes and Metabolism

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/andr.12390/fullpdf

Reference54 articles.

1. Gain-off-unction mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome;Aoki;Am J Hum Genet,2013

2. Recent advances in RASopathies;Aoki;J Hum Genet,2016

3. Linkage between cryptorchidism, hypospadias, and GGN repeat length in the androgen receptor gene;Aschim;J Clin Endocrinol Metab,2004

4. Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functions;Barthold;Hum Reprod,2015

5. Polygenic inheritance of cryptorchidism susceptibility in the LE/orl rat;Barthold;Mol Hum Reprod,2016

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