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E M Stone

Showing results (151-160 of 174) with videos related to

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Investigative Ophthalmology & Visual Science|May 8, 2000
Allelic variation in the VMD2 gene in best disease and age-related macular degenerationA J Lotery, F L Munier, G A Fishman, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Ophthalmology|September 6, 2001
Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifierJ E Craig, P N Baird, D L Healey, et al.
The New England Journal of Medicine|April 16, 1998
Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)W L Alward, J H Fingert, M A Coote, et al.
Investigative Ophthalmology & Visual Science|June 14, 2000
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosaS G Jacobson, A V Cideciyan, A Iannaccone, et al.
Science (New York, N.Y.)|June 6, 1998
Mutations in the SMAD4/DPC4 gene in juvenile polyposisJ R Howe, S Roth, J C Ringold, et al.
Gene Therapy|May 9, 2014
CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotypeE R Burnight, L A Wiley, A V Drack, et al.
Human Molecular Genetics|January 12, 2001
Non-secretion of mutant proteins of the glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humorN Jacobson, M Andrews, A R Shepard, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001
Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.
Pageof 18

Showing results (151-160 of 174) with videos related to

Sort By:
Pageof 18
Investigative Ophthalmology & Visual Science|May 8, 2000
Allelic variation in the VMD2 gene in best disease and age-related macular degenerationA J Lotery, F L Munier, G A Fishman, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Ophthalmology|September 6, 2001
Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifierJ E Craig, P N Baird, D L Healey, et al.
The New England Journal of Medicine|April 16, 1998
Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)W L Alward, J H Fingert, M A Coote, et al.
Investigative Ophthalmology & Visual Science|June 14, 2000
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosaS G Jacobson, A V Cideciyan, A Iannaccone, et al.
Science (New York, N.Y.)|June 6, 1998
Mutations in the SMAD4/DPC4 gene in juvenile polyposisJ R Howe, S Roth, J C Ringold, et al.
Gene Therapy|May 9, 2014
CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotypeE R Burnight, L A Wiley, A V Drack, et al.
Human Molecular Genetics|January 12, 2001
Non-secretion of mutant proteins of the glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humorN Jacobson, M Andrews, A R Shepard, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001
Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.
Pageof 18