INHERITED RETINAL DISEASE LABORATORY STUDIES: MOLECULAR GENETIC RESEARCH PROJECTS

Code

Project Title

Researcher

Funder

Start Date

End Date

ALIR1001

Gene therapy for retinal degeneration

Mr R Ali

Wellcome Trust

01/04/1999

31/03/2001

BHAS1001

Autosomal dominant retinitis pigmentosa:positional cloning of novel ADRP genes on chromosome 7P and 19q and further genetic linkage studies to identify new loci

Professor S S Bhattacharya

Foundation Fighting Blindness

01/09/1996

31/08/1999

BHAS1002

The identification, cloning and characterisation of a dominant Retinitis Pigmentosa gene on chromosome 19q

Professor S S Bhattacharya

Wellcome Trust

01/02/1995

31/08/1999

BHAS1004

Positional cloning of the X-linked retinitis pigmentosa 2 (RP2) gene

Professor S S Bhattacharya

Wellcome Trust

01/10/1997

30/09/2000

BHAS1005

Autosomal dominant retinitis pigmentosa: Identification of new loci by genetic lingage studies and positional cloning of RP genes from chromosomes 19q (RP11), 7q (RP13) and 1q (RP18)

Professor S S Bhattacharya

Foundation Fighting Blindness

01/09/1999

31/08/2001

BIRA1002

Characterisation of functional loss in outer retinal dystrophies with known genetic mutations

Professor A C Bird

Medical Research Council

01/10/1993

30/09/2000

BIRA1003

Characterization of phenotype in age related macular disease in patients with unilateral visual loss [Detail]

Professor A C Bird

01/04/1998

31/03/2001

DACL1001

The phenotype-genotype relationship of inherited macular dystrophies in families from Moorfields genetic register

L Da Cruz

Royal Society

01/03/2000

28/02/2002

GILC1004

Congenital anomalies of the eye in children: a pilot study to explore the association between mutations in genes controlling retinoic acid signalling and ocular malformations

Mr C Gilbert

Task Force

01/12/1999

31/12/2000

HUND1001

Cone and cone-rod dystrophies in man: screening of candidate genes and functional analysis of mutant proteins

D M Hunt

Wellcome Trust

01/09/1998

30/06/2000

HUND1002

A study of the role of homologues of visual transduction and eye development genes

D M Hunt

Wellcome Trust

01/03/1996

31/07/1999

HUND1004

The regulation of opsin gene expressionin retinal rods

D M Hunt

BBSRC

01/11/1999

31/10/2002

MEHS1001

Molecular genetic studies of families with retinal degeneration

S Q Mehdi

Wellcome Trust

01/11/1996

31/10/1999

MOOA1001

Cone rod dystrophies in man; linkage and candidate genes [Detail]

Mr AT Moore

Wellcome Trust

01/11/1994

31/10/1999

VOTM1001

A clinical and molecular genetic analysis of dominant optic atrophy [Detail]

Miss M Votruba

Guide Dogs for the Blind Association

01/04/1996

01/04/2000

VOTM1002

Cloning and characterisation of the chromosome 3q28 dominant optic atrophy gene (OPA1)

Miss M Votruba

Wellcome Trust

01/01/1999

31/12/2000

VOTM1003

Identification and characterisation of the gene for autosomal dominant optic atrophy (OPA 1) mapping to chromosome 3q28-qter

Miss M Votruba

British Council

01/07/1999

31/03/2001

VOTM1004

Autosomal dominant optic atrophy: positional cloning of OPA1 gene on chromosome 3q

Miss M Votruba

Wellcome Trust

01/12/1996

30/11/1999

WEBA1001

A study of phenotype-genotype corelation in ophthalmic genetic disease

Mr A Webster

TFC Frost

01/11/1997

31/10/1999