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Results: 1 to 20 of 245

Similar articles for PubMed (Select 23922489)

1.

Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish population.

Millá E, Mañé B, Duch S, Hernan I, Borràs E, Planas E, Dias Mde S, Carballo M, Gamundi MJ; Spanish Multicenter Glaucoma Group-Estudio Multicéntrico Español de Investigación Genética del Glaucoma, EMEIGG.

Mol Vis. 2013 Aug 4;19:1707-22. Print 2013.

2.

Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1.

Hilal L, Boutayeb S, Serrou A, Refass-Buret L, Shisseh H, Bencherifa F, El Mzibri M, Benazzouz B, Berraho A.

Mol Vis. 2010 Jul 2;16:1215-26.

3.

Mutation spectrum of CYP1B1 and MYOC genes in Korean patients with primary congenital glaucoma.

Kim HJ, Suh W, Park SC, Kim CY, Park KH, Kook MS, Kim YY, Kim CS, Park CK, Ki CS, Kee C.

Mol Vis. 2011;17:2093-101. Epub 2011 Aug 9.

4.

Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene.

Vincent AL, Billingsley G, Buys Y, Levin AV, Priston M, Trope G, Williams-Lyn D, Héon E.

Am J Hum Genet. 2002 Feb;70(2):448-60. Epub 2002 Jan 3.

5.

MYOC gene mutations in Spanish patients with autosomal dominant primary open-angle glaucoma: a founder effect in southeast Spain.

Campos-Mollo E, Sánchez-Sánchez F, López-Garrido MP, López-Sánchez E, López-Martínez F, Escribano J.

Mol Vis. 2007 Sep 13;13:1666-73.

6.

The novel heterozygous Thr377Arg MYOC mutation causes severe Juvenile Open Angle Glaucoma in a large Pakistani family.

Waryah AM, Narsani AK, Sheikh SA, Shaikh H, Shahani MY.

Gene. 2013 Oct 10;528(2):356-9. doi: 10.1016/j.gene.2013.07.016. Epub 2013 Jul 23.

PMID:
23886590
7.

CYP1B1 mutations in French patients with early-onset primary open-angle glaucoma.

Melki R, Colomb E, Lefort N, Brézin AP, Garchon HJ.

J Med Genet. 2004 Sep;41(9):647-51.

8.

Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation.

Abu-Amero KK, Osman EA, Mousa A, Wheeler J, Whigham B, Allingham RR, Hauser MA, Al-Obeidan SA.

Mol Vis. 2011;17:2911-9. Epub 2011 Nov 12.

9.

Mutational screening of CYP1B1 in Turkish PCG families and functional analyses of newly detected mutations.

Bagiyeva S, Marfany G, Gonzalez-Angulo O, Gonzalez-Duarte R.

Mol Vis. 2007 Aug 27;13:1458-68.

10.

A clinical and molecular genetics study of primary congenital glaucoma in South Korea.

Suh W, Kee C.

Br J Ophthalmol. 2012 Nov;96(11):1372-7. doi: 10.1136/bjophthalmol-2012-301517. Epub 2012 Sep 1.

PMID:
22942166
11.

A novel MYOC heterozygous mutation identified in a Chinese Uygur pedigree with primary open-angle glaucoma.

Cai SP, Muhemaiti P, Yin Y, Cheng H, Di Ya A, Keyimu M, Cao X, Fan N, Jiang L, Yan N, Zhou X, Wang Y, Liu X.

Mol Vis. 2012;18:1944-51. Epub 2012 Jul 18.

12.

Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol.

Suri F, Kalhor R, Zargar SJ, Nilforooshan N, Yazdani S, Nezari H, Paylakhi SH, Narooie-Nejhad M, Bayat B, Sedaghati T, Ahmadian A, Elahi E.

Mol Vis. 2008;14:2349-56. Epub 2008 Dec 18.

13.

A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG).

El-Ashry MF, Abd El-Aziz MM, Bhattacharya SS.

J Glaucoma. 2007 Jan;16(1):104-11.

PMID:
17224759
14.

CYP1B1 and MYOC mutations in 116 Chinese patients with primary congenital glaucoma.

Chen Y, Jiang D, Yu L, Katz B, Zhang K, Wan B, Sun X.

Arch Ophthalmol. 2008 Oct;126(10):1443-7. doi: 10.1001/archopht.126.10.1443.

PMID:
18852424
15.

Genetics of primary glaucoma.

Khan AO.

Curr Opin Ophthalmol. 2011 Sep;22(5):347-55. doi: 10.1097/ICU.0b013e32834922d2. Review.

PMID:
21730848
16.

Role of CYP1B1, MYOC, OPTN, and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients.

Kumar A, Basavaraj MG, Gupta SK, Qamar I, Ali AM, Bajaj V, Ramesh TK, Prakash DR, Shetty JS, Dorairaj SK.

Mol Vis. 2007 Apr 30;13:667-76.

17.

Primary role of CYP1B1 in Indian juvenile-onset POAG patients.

Acharya M, Mookherjee S, Bhattacharjee A, Bandyopadhyay AK, Daulat Thakur SK, Bhaduri G, Sen A, Ray K.

Mol Vis. 2006 Apr 20;12:399-404.

18.

CYP1B1, MYOC, and LTBP2 mutations in primary congenital glaucoma patients in the United States.

Lim SH, Tran-Viet KN, Yanovitch TL, Freedman SF, Klemm T, Call W, Powell C, Ravichandran A, Metlapally R, Nading EB, Rozen S, Young TL.

Am J Ophthalmol. 2013 Mar;155(3):508-517.e5. doi: 10.1016/j.ajo.2012.09.012. Epub 2012 Dec 4.

19.

Contributions of MYOC and CYP1B1 mutations to JOAG.

Bayat B, Yazdani S, Alavi A, Chiani M, Chitsazian F, Tusi BK, Suri F, Narooie-Nejhad M, Sanati MH, Elahi E.

Mol Vis. 2008 Mar 13;14:508-17.

20.

Novel and known MYOC exon 3 mutations in an admixed Peruvian primary open-angle glaucoma population.

Mendoza-Reinoso V, Patil TS, Guevara-Fujita ML, Fernández S, Vargas E, Castillo-Herrera W, Perez-Grossmann R, Lizaraso-Caparó F, Richards JE, Fujita R.

Mol Vis. 2012;18:2067-75. Epub 2012 Aug 8.

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