Literature DB >> 14619973

Recent advances in molecular genetics of glaucoma.

Kunal Ray1, Arijit Mukhopadhyay, Moulinath Acharya.   

Abstract

Glaucoma represents a heterogeneous group of optic neuropathies, with different genetic bases. It can affect all ages generally with a rise in intra-ocular pressure. Three major types of glaucoma have been reported: primary open angle glaucoma (POAG), primary acute closed angle glaucoma (PACG) and primary congenital glaucoma (PCG), as well as a few others associated with developmental abnormalities. In recent years impressive progress has been made in the molecular genetic studies of POAG and PCG. These include the discovery of three genes--Myocilin, Optineurin and CYP1B1--defects in which results in Mendelian transmission of glaucoma. Identification of single nucleotide polymorphisms in multiple other genes that are associated with glaucoma and alteration of drug sensitivity are enriching our knowledge regarding the complex nature of the disease. This review attempts to present the recent progress made in the molecular genetics of glaucoma.

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Year:  2003        PMID: 14619973     DOI: 10.1023/a:1026059800470

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  84 in total

1.  Myocilin mutation 1109 C>T (Pro 370 Leu) is the most common gene defect causing early onset primary open angle glaucoma.

Authors:  Arijit Mukhopadhyay; Moulinath Acharya; Jharna Ray; Mita Khan; Krishnendu Sarkar; Asit Ranjan Banerjee; Kunal Ray
Journal:  Indian J Ophthalmol       Date:  2003-09       Impact factor: 1.848

2.  GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36.

Authors:  M K Wirtz; J R Samples; K Rust; J Lie; L Nordling; K Schilling; T S Acott; P L Kramer
Journal:  Arch Ophthalmol       Date:  1999-02

3.  Founder effect in GLC1A-linked familial open-angle glaucoma in Northern France.

Authors:  A P Brézin; M F Adam; A Belmouden; M A Lureau; A Chaventré; B Copin; L Gomez; S D De Dinechin; M Berkani; F Valtot; J F Rouland; J C Dascotte; J F Bach; H J Garchon
Journal:  Am J Med Genet       Date:  1998-04-13

Review 4.  Recent advances in molecular genetics of glaucomas.

Authors:  M Sarfarazi
Journal:  Hum Mol Genet       Date:  1997       Impact factor: 6.150

5.  Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome.

Authors:  S D Dreyer; G Zhou; A Baldini; A Winterpacht; B Zabel; W Cole; R L Johnson; B Lee
Journal:  Nat Genet       Date:  1998-05       Impact factor: 38.330

6.  Association of a single nucleotide polymorphism in the TIGR/MYOCILIN gene promoter with the severity of primary open-angle glaucoma.

Authors:  E Colomb; T D Nguyen; A Béchetoille; J C Dascotte; F Valtot; A P Brézin; M Berkani; B Copin; L Gomez; J R Polansky; H J Garchon
Journal:  Clin Genet       Date:  2001-09       Impact factor: 4.438

7.  A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.

Authors:  L Morlé; M Bozon; J C Zech; N Alloisio; A Raas-Rothschild; C Philippe; J C Lambert; J Godet; H Plauchu; P Edery
Journal:  Am J Hum Genet       Date:  2000-10-13       Impact factor: 11.025

8.  Promoter mutations of myocilin gene in Japanese patients with open angle glaucoma including normal tension glaucoma.

Authors:  R Suzuki; Y Hattori; K Okano
Journal:  Br J Ophthalmol       Date:  2000-09       Impact factor: 4.638

9.  Mutations in MYOC gene of Indian primary open angle glaucoma patients.

Authors:  Arijit Mukhopadhyay; Moulinath Acharya; Saibal Mukherjee; Jharna Ray; Sumit Choudhury; Mita Khan; Kunal Ray
Journal:  Mol Vis       Date:  2002-11-15       Impact factor: 2.367

Review 10.  Primary infantile glaucoma (congenital glaucoma).

Authors:  V P deLuise; D R Anderson
Journal:  Surv Ophthalmol       Date:  1983 Jul-Aug       Impact factor: 6.048

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  16 in total

1.  Expression, purification, crystallization and preliminary X-ray analysis of the olfactomedin domain from the sea urchin cell-adhesion protein amassin.

Authors:  Brian J Hillier; Vidyasankar Sundaresan; C David Stout; Victor D Vacquier
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2005-12-16

2.  CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.

Authors:  Fereshteh Chitsazian; Betsabeh Khoramian Tusi; Elahe Elahi; Heidar Amini Saroei; Mohammad H Sanati; Shahin Yazdani; Mohammad Pakravan; Navid Nilforooshan; Yadollah Eslami; Mohammad Ali Zare Mehrjerdi; Reza Zareei; Mahmood Jabbarvand; Ali Abdolahi; Ali R Lasheyee; Arash Etemadi; Behnaz Bayat; Mehdi Sadeghi; Mohammad M Banoei; Behnam Ghafarzadeh; Mohammad R Rohani; Akram Rismanchian; Yvonne Thorstenson; Mansoor Sarfarazi
Journal:  J Mol Diagn       Date:  2007-07       Impact factor: 5.568

3.  Molecular cloning of the m-Golsyn gene and its expression in the mouse brain.

Authors:  Eishi Funakoshi; Ayako Hamano; Masaki Fukui; Norito Nishiyama; Kiyokazu Ogita; Nobuyoshi Shimizu; Fumiaki Ito
Journal:  Gene Expr       Date:  2006

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

Authors:  Latifa Hilal; Soraya Boutayeb; Aziza Serrou; Loubna Refass-Buret; Hafsa Shisseh; Fatiha Bencherifa; Mohammed El Mzibri; Bouchra Benazzouz; Amina Berraho
Journal:  Mol Vis       Date:  2010-07-02       Impact factor: 2.367

Review 5.  Molecular complexity of primary open angle glaucoma: current concepts.

Authors:  Kunal Ray; Suddhasil Mookherjee
Journal:  J Genet       Date:  2009-12       Impact factor: 1.166

Review 6.  Glaucoma in iran and contributions of studies in iran to the understanding of the etiology of glaucoma.

Authors:  Fatemeh Suri; Shahin Yazdani; Elahe Elahi
Journal:  J Ophthalmic Vis Res       Date:  2015 Jan-Mar

7.  Screening of the LTBP2 gene in a north Indian population with primary congenital glaucoma.

Authors:  Kuldeep Mohanty; Mukesh Tanwar; Rima Dada; Tanuj Dada
Journal:  Mol Vis       Date:  2013-01-17       Impact factor: 2.367

8.  Contribution of the latent transforming growth factor-β binding protein 2 gene to etiology of primary open angle glaucoma and pseudoexfoliation syndrome.

Authors:  Sahar Jelodari-Mamaghani; Ramona Haji-Seyed-Javadi; Fatemeh Suri; Naveed Nilforushan; Shahin Yazdani; Kambiz Kamyab; Elahe Elahi
Journal:  Mol Vis       Date:  2013-02-07       Impact factor: 2.367

9.  Contributions of MYOC and CYP1B1 mutations to JOAG.

Authors:  Behnaz Bayat; Shahin Yazdani; Afagh Alavi; Mohsen Chiani; Fereshteh Chitsazian; Betsabeh Khoramian Tusi; Fatemeh Suri; Mehrnaz Narooie-Nejhad; Mohammad H Sanati; Elahe Elahi
Journal:  Mol Vis       Date:  2008-03-13       Impact factor: 2.367

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

Authors:  Fatemeh Suri; Reza Kalhor; Seyed Jalal Zargar; Navid Nilforooshan; Shahin Yazdani; Hossein Nezari; Seyed Hassan Paylakhi; Mehrnaz Narooie-Nejhad; Behnaz Bayat; Tina Sedaghati; Afshin Ahmadian; Elahe Elahi
Journal:  Mol Vis       Date:  2008-12-18       Impact factor: 2.367

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