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E M Stone

Showing results (111-120 of 174) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|June 17, 1998
Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in manA V Cideciyan, D C Hood, Y Huang, et al.
Pharmacogenetics|July 27, 2001
N-Acetyltransferases, sulfotransferases and heterocyclic amine activation in the breastJ A Williams, E M Stone, G Fakis, et al.
Human Molecular Genetics|April 1, 1997
Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase geneA Nystuen, H Costeff, O N Elpeleg, et al.
Genome Research|June 13, 1998
Characterization and comparison of the human and mouse GLC1A glaucoma genesJ H Fingert, L Ying, R E Swiderski, et al.
Molecular Vision|November 17, 1999
What can we learn about age-related macular degeneration from other retinal diseases?D J Zack, M Dean, R S Molday, et al.
Ophthalmic Genetics|September 18, 2001
CRB1 mutations may result in retinitis pigmentosa without para-arteriolar RPE preservationA J Lotery, A Malik, S A Shami, et al.
Molecular Vision|April 26, 2001
Optimal procedure for extracting RNA from human ocular tissues and expression profiling of the congenital glaucoma gene FOXC1 using quantitative RT-PCRW H Wang, L G McNatt, A R Shepard, et al.
American Journal of Human Genetics|June 1, 1996
A mutation causing Alport syndrome with tardive hearing loss is common in the western United StatesD F Barker, C J Pruchno, X Jiang, et al.
Ophthalmic Genetics|December 1, 1996
Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin geneB Piguet, E Héon, F L Munier, et al.
Ophthalmology|February 1, 1995
A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degenerationM B Gorin, K E Jackson, R E Ferrell, et al.
Pageof 18

Showing results (111-120 of 174) with videos related to

Sort By:
Pageof 18
Proceedings of the National Academy of Sciences of the United States of America|June 17, 1998
Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in manA V Cideciyan, D C Hood, Y Huang, et al.
Pharmacogenetics|July 27, 2001
N-Acetyltransferases, sulfotransferases and heterocyclic amine activation in the breastJ A Williams, E M Stone, G Fakis, et al.
Human Molecular Genetics|April 1, 1997
Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase geneA Nystuen, H Costeff, O N Elpeleg, et al.
Genome Research|June 13, 1998
Characterization and comparison of the human and mouse GLC1A glaucoma genesJ H Fingert, L Ying, R E Swiderski, et al.
Molecular Vision|November 17, 1999
What can we learn about age-related macular degeneration from other retinal diseases?D J Zack, M Dean, R S Molday, et al.
Ophthalmic Genetics|September 18, 2001
CRB1 mutations may result in retinitis pigmentosa without para-arteriolar RPE preservationA J Lotery, A Malik, S A Shami, et al.
Molecular Vision|April 26, 2001
Optimal procedure for extracting RNA from human ocular tissues and expression profiling of the congenital glaucoma gene FOXC1 using quantitative RT-PCRW H Wang, L G McNatt, A R Shepard, et al.
American Journal of Human Genetics|June 1, 1996
A mutation causing Alport syndrome with tardive hearing loss is common in the western United StatesD F Barker, C J Pruchno, X Jiang, et al.
Ophthalmic Genetics|December 1, 1996
Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin geneB Piguet, E Héon, F L Munier, et al.
Ophthalmology|February 1, 1995
A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degenerationM B Gorin, K E Jackson, R E Ferrell, et al.
Pageof 18