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Scholar Results 1 - 6 of 6 citing Dietrich: A novel mutation of the RP1 gene (Lys778ter) associated with autosomal dominant.... (0.09 sec) 

RP1 is required for the correct stacking of outer segment discs

- iovs.org
Q Liu, A Lyubarsky, JH Skalet, EN Pugh Jr, EA … - Investigative ophthalmology & visual science, 2003 - ARVO
PURPOSE. Mutations in RP1 are a common cause of dominant retinitis pigmentosa
(RP), but the mechanism by which the identified mutations lead to photoreceptor
cell death and blindness has not been determined. To investigate the ...
Cited by 22 - Related articles - BL Direct - All 5 versions

The clinical applications of multifocal electroretinography: a systematic review


TYY Lai, WM Chan, RYK Lai, JWS Ngai, H Li … - Survey of ophthalmology, 2007 - Elsevier
Multifocal electroretinography (mfERG) is an investigation that can
simultaneously measure multiple electroretinographic responses at different
retinal locations by cross-correlation techniques. mfERG therefore allows ...
Cited by 15 - Related articles - All 12 versions

Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa

- bmj.com [PDF] 
S Khaliq, A Abid, M Ismail, A Hameed, A … - British Medical Journal, 2005 - jmg.bmj.com
Novel association of RP1 gene mutations with autosomal ... S Khaliq, A Abid, M
Ismail, A Hameed, A Mohyuddin, P Lall, A Aziz, K Anwar, SQ Mehdi ...............
............................................................................ ...
Cited by 10 - Related articles - All 6 versions

Molecular consequences of dominant Bethlem myopathy collagen VI mutations


NL Baker, M Morgelin, RA Pace, RA Peat, NE … - Annals of Neurology, 2007 - interscience.wiley.com
It is also possible that your web browser is not configured or not able to
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Cited by 9 - Related articles - BL Direct - All 3 versions

RP1 Consortium. Identification of the RP1 and RP10 (IMPDH1) genes causing autosomal …

- tcd.ie [PDF] 
P HUMPHRIES, 2003 - tara.tcd.ie
1 Human Genetics Center and Dept. of Ophthalmology, The Univ. of Texas, Houston;
TX, USA ... Genetics Unit, Trinity College, Dublin, Ireland 3 Retina Foundation
of the Southwest, Dallas, TX, USA ... Stein Eye Inst., The Univ. of ...
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IDENTIFICATION OF THE RP1 AND RP10 (IMPDH1) GENES CAUSING AUTOSOMAL …


SP Daiger, LS Sullivan, SJ Bowne, A Kennan, … - Advances in experimental medicine and biology, 2003 - pubmedcentral.nih.gov
In a project begun more than 15 years ago we used linkage mapping and positional
candidate gene cloning to identify two genes causing autosomal dominant
retinitis pigmentosa (adRP). The genes are RP1, which maps to chromosome ...
Related articles - BL Direct - All 2 versions


 


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