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Showing results (141-150 of 153) with videos related to

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Investigative Ophthalmology & Visual Science|May 1, 2001
An analysis of allelic variation in the ABCA4 geneA R Webster, E Héon, A J Lotery, et al.
Human Molecular Genetics|November 2, 2001
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophyS Biswas, F L Munier, J Yardley, et al.
Science (New York, N.Y.)|January 31, 1997
Identification of a gene that causes primary open angle glaucomaE M Stone, J H Fingert, W L Alward, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 15, 2000
Mutation analysis of 3 genes in patients with Leber congenital amaurosisA J Lotery, P Namperumalsamy, S G Jacobson, et al.
Genome Research|October 6, 1997
Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21J H Greinwald, D A Scott, J R Marietta, et al.
Nature Genetics|February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fateN B Haider, S G Jacobson, A V Cideciyan, et al.
Nature Genetics|May 31, 2001
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4K Mykytyn, T Braun, R Carmi, et al.
Investigative Ophthalmology & Visual Science|June 30, 2001
Glucocorticoid induction of the glaucoma gene MYOC in human and monkey trabecular meshwork cells and tissuesA F Clark, H T Steely, J E Dickerson, et al.
Human Molecular Genetics|April 10, 1999
Analysis of myocilin mutations in 1703 glaucoma patients from five different populationsJ H Fingert, E Héon, J M Liebmann, et al.
Pageof 16

Showing results (141-150 of 153) with videos related to

Sort By:
Pageof 16
Investigative Ophthalmology & Visual Science|May 1, 2001
An analysis of allelic variation in the ABCA4 geneA R Webster, E Héon, A J Lotery, et al.
Human Molecular Genetics|November 2, 2001
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophyS Biswas, F L Munier, J Yardley, et al.
Science (New York, N.Y.)|January 31, 1997
Identification of a gene that causes primary open angle glaucomaE M Stone, J H Fingert, W L Alward, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 15, 2000
Mutation analysis of 3 genes in patients with Leber congenital amaurosisA J Lotery, P Namperumalsamy, S G Jacobson, et al.
Genome Research|October 6, 1997
Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21J H Greinwald, D A Scott, J R Marietta, et al.
Nature Genetics|February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fateN B Haider, S G Jacobson, A V Cideciyan, et al.
Nature Genetics|May 31, 2001
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4K Mykytyn, T Braun, R Carmi, et al.
Investigative Ophthalmology & Visual Science|June 30, 2001
Glucocorticoid induction of the glaucoma gene MYOC in human and monkey trabecular meshwork cells and tissuesA F Clark, H T Steely, J E Dickerson, et al.
Human Molecular Genetics|April 10, 1999
Analysis of myocilin mutations in 1703 glaucoma patients from five different populationsJ H Fingert, E Héon, J M Liebmann, et al.
Pageof 16