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Gene Therapy|February 4, 1999
Co-injection of adenovirus expressing CTLA4-Ig prolongs adenovirally mediated lacZ reporter gene expression in the mouse retinaR R Ali, M B Reichel, A P Byrnes, et al.The British Journal of Ophthalmology|August 1, 1992
Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutationA T Moore, F W Fitzke, C M Kemp, et al.Journal of Medical Genetics|November 1, 1994
Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 lociM A Aldred, P W Teague, M Jay, et al.American Journal of Human Genetics|January 22, 2003
The genetic heritage of the earliest settlers persists both in Indian tribal and caste populationsT Kivisild, S Rootsi, M Metspalu, et al.American Journal of Human Genetics|April 1, 1994
Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9)C F Inglehearn, T J Keen, M al-Maghtheh, et al.The British Journal of Ophthalmology|January 25, 2003
A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphylomaM A Reddy, P J Francis, V Berry, et al.Journal of Neurology|February 1, 1993
The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalitiesK M Bushby, D Gardner-Medwin, L V Nicholson, et al.Human Genetics|March 10, 1999
Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD)S Kermani, K Gregory-Evans, E E Tarttelin, et al.Investigative Ophthalmology & Visual Science|October 23, 1997
Single exposures to antiproliferatives: long-term effects on ocular fibroblast wound-healing behaviorN L Occleston, J T Daniels, R W Tarnuzzer, et al.Human Gene Therapy|February 11, 1998
Adeno-associated virus gene transfer to mouse retinaR R Ali, M B Reichel, M De Alwis, et al.Pageof 37