Maya-Nuñez G - Search Results

1

A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome.

Maya-Nuñez G, Zenteno JC, Ulloa-Aguirre A, Kofman-Alfaro S, Mendez JP. Maya-Nuñez G, et al. J Clin Endocrinol Metab. 1998 May;83(5):1650-3. doi: 10.1210/jcem.83.5.4817. J Clin Endocrinol Metab. 1998. PMID: 9589672

2

Molecular basis of hypogonadotropic hypogonadism: restoration of mutant (E(90)K) GnRH receptor function by a deletion at a distant site.

Maya-Núñez G, Janovick JA, Ulloa-Aguirre A, Söderlund D, Conn PM, Méndez JP. Maya-Núñez G, et al. J Clin Endocrinol Metab. 2002 May;87(5):2144-9. doi: 10.1210/jcem.87.5.8386. J Clin Endocrinol Metab. 2002. PMID: 11994356

3

Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene.

Maya-Núñez G, Cuevas-Covarrubias S, Zenteno JC, Ulloa-Aguirre A, Kofman-Alfaro S, Méndez JP. Maya-Núñez G, et al. Clin Endocrinol (Oxf). 1998 Jun;48(6):713-8. doi: 10.1046/j.1365-2265.1998.00406.x. Clin Endocrinol (Oxf). 1998. PMID: 9713559

4

An atypical contiguous gene syndrome: molecular studies in a family with X-linked Kallmann's syndrome and X-linked ichthyosis.

Maya-Nuñez G, Torres L, Ulloa-Aguirre A, Zenteno JC, Cuevas-Covarrubias S, Saavedra-Ontiveros D, Kofman-Alfaro S, Méndez JP. Maya-Nuñez G, et al. Clin Endocrinol (Oxf). 1999 Feb;50(2):157-62. doi: 10.1046/j.1365-2265.1999.00588.x. Clin Endocrinol (Oxf). 1999. PMID: 10396356

5

Renal abnormalities in patients with Kallmann syndrome.

Zenteno JC, Méndez JP, Maya-Núñez G, Ulloa-Aguirre A, Kofman-Alfaro S. Zenteno JC, et al. BJU Int. 1999 Mar;83(4):383-6. doi: 10.1046/j.1464-410x.1999.00027.x. BJU Int. 1999. PMID: 10210557

6

CRH-stimulation of cyclic adenosine 5'-monophosphate pathway is partially inhibited by the coexpression of CRH-R1 and CRH-R2alpha.

Maya-Núñez G, Castro-Fernández C, Méndez JP. Maya-Núñez G, et al. Endocrine. 2005 Jun;27(1):67-73. doi: 10.1385/endo:27:1:067. Endocrine. 2005. PMID: 16077174

7

Regulation of follicle-stimulating and luteinizing hormone receptor signaling by.

Castro-Fernández C, Maya-Núñez G, Méndez JP. Castro-Fernández C, et al. Endocrine. 2004 Oct;25(1):49-54. doi: 10.1385/endo:25:1:49. Endocrine. 2004. PMID: 15545706

8

Conformational effects of Lys191 in the human GnRH receptor: mutagenesis and molecular dynamics simulations studies.

Jardón-Valadez E, Aguilar-Rojas A, Maya-Núñez G, Leaños-Miranda A, Piñeiro A, Conn PM, Ulloa-Aguirre A. Jardón-Valadez E, et al. J Endocrinol. 2009 May;201(2):297-307. doi: 10.1677/JOE-08-0527. Epub 2009 Feb 26. J Endocrinol. 2009. PMID: 19246515 Free PMC article.

9

Biochemical mechanism of pathogenesis of human gonadotropin-releasing hormone receptor mutants Thr104Ile and Tyr108Cys associated with familial hypogonadotropic hypogonadism.

Maya-Núñez G, Janovick JA, Aguilar-Rojas A, Jardón-Valadez E, Leaños-Miranda A, Zariñan T, Ulloa-Aguirre A, Conn PM. Maya-Núñez G, et al. Mol Cell Endocrinol. 2011 Apr 30;337(1-2):16-23. doi: 10.1016/j.mce.2011.01.016. Epub 2011 Jan 26. Mol Cell Endocrinol. 2011. PMID: 21277937 Free PMC article.

10

Dominant negative effects of human follicle-stimulating hormone receptor expression-deficient mutants on wild-type receptor cell surface expression. Rescue of oligomerization-dependent defective receptor expression by using cognate decoys.

Zariñán T, Perez-Solís MA, Maya-Núñez G, Casas-González P, Conn PM, Dias JA, Ulloa-Aguirre A. Zariñán T, et al. Among authors: maya nunez g. Mol Cell Endocrinol. 2010 Jun 10;321(2):112-22. doi: 10.1016/j.mce.2010.02.027. Epub 2010 Mar 4. Mol Cell Endocrinol. 2010. PMID: 20206665 Free PMC article.

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