Zenteno JC - Search Results

1

Mutations in a novel serine protease PRSS56 in families with nanophthalmos.

Orr A, Dubé MP, Zenteno JC, Jiang H, Asselin G, Evans SC, Caqueret A, Lakosha H, Letourneau L, Marcadier J, Matsuoka M, Macgillivray C, Nightingale M, Papillon-Cavanagh S, Perry S, Provost S, Ludman M, Guernsey DL, Samuels ME. Orr A, et al. Among authors: zenteno jc. Mol Vis. 2011;17:1850-61. Epub 2011 Jul 12. Mol Vis. 2011. PMID: 21850159 Free PMC article.

2

A new autosomal recessive syndrome consisting of posterior microphthalmos, retinitis pigmentosa, foveoschisis, and optic disc drusen is caused by a MFRP gene mutation.

Ayala-Ramirez R, Graue-Wiechers F, Robredo V, Amato-Almanza M, Horta-Diez I, Zenteno JC. Ayala-Ramirez R, et al. Among authors: zenteno jc. Mol Vis. 2006 Dec 4;12:1483-9. Mol Vis. 2006. PMID: 17167404 Free article.

3

The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.

Correa-Gomez V, Villalvazo-Cordero L, Zenteno JC. Correa-Gomez V, et al. Among authors: zenteno jc. Mol Vis. 2007 Sep 17;13:1695-700. Mol Vis. 2007. PMID: 17893671

4

Familial Wolfram syndrome due to compound heterozygosity for two novel WFS1 mutations.

Zenteno JC, Ruiz G, Pérez-Cano HJ, Camargo M. Zenteno JC, et al. Mol Vis. 2008 Jul 25;14:1353-7. Mol Vis. 2008. PMID: 18660851 Free PMC article.

5

Compound heterozygosity for a novel and a recurrent MFRP gene mutation in a family with the nanophthalmos-retinitis pigmentosa complex.

Zenteno JC, Buentello-Volante B, Quiroz-González MA, Quiroz-Reyes MA. Zenteno JC, et al. Mol Vis. 2009 Sep 5;15:1794-8. Mol Vis. 2009. PMID: 19753314 Free PMC article.

6

Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.

Ali M, Buentello-Volante B, McKibbin M, Rocha-Medina JA, Fernandez-Fuentes N, Koga-Nakamura W, Ashiq A, Khan K, Booth AP, Williams G, Raashid Y, Jafri H, Rice A, Inglehearn CF, Zenteno JC. Ali M, et al. Among authors: zenteno jc. Mol Vis. 2010 Jun 23;16:1162-8. Mol Vis. 2010. PMID: 20664696 Free PMC article.

7

Membrane frizzled-related protein gene-related ophthalmological syndrome: 30-month follow-up of a sporadic case and review of genotype-phenotype correlation in the literature.

Neri A, Leaci R, Zenteno JC, Casubolo C, Delfini E, Macaluso C. Neri A, et al. Among authors: zenteno jc. Mol Vis. 2012;18:2623-32. Epub 2012 Oct 26. Mol Vis. 2012. PMID: 23112574 Free PMC article.

8

An epidemiological investigation of a Forkhead box protein E3 founder mutation underlying the high frequency of sclerocornea, aphakia, and microphthalmia in a Mexican village.

Pantoja-Melendez C, Ali M, Zenteno JC. Pantoja-Melendez C, et al. Among authors: zenteno jc. Mol Vis. 2013 Aug 27;19:1866-70. eCollection 2013. Mol Vis. 2013. PMID: 24019743 Free PMC article.

9

CRYGD gene analysis in a family with autosomal dominant congenital cataract: evidence for molecular homogeneity and intrafamilial clinical heterogeneity in aculeiform cataract.

Zenteno JC, Morales ME, Moran-Barroso V, Sanchez-Navarro A. Zenteno JC, et al. Mol Vis. 2005 Jun 30;11:438-42. Mol Vis. 2005. PMID: 16030500 Free article.

10

PAX6 gene intragenic deletions in Mexican patients with congenital aniridia.

Ramirez-Miranda A, Zenteno JC. Ramirez-Miranda A, et al. Among authors: zenteno jc. Mol Vis. 2006 Apr 7;12:318-23. Mol Vis. 2006. PMID: 16617299 Free article.

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