D M Hunt|A E Port - JoVE Visualize

Showing results (111-120 of 145) with videos related to

Pageof 15

Sort By:

The American Journal of Physiology|May 1, 1991

Abnormal epithelial transport in cystic fibrosis jejunumE V O'Loughlin, D M Hunt, K J Gaskin, et al.

Genomics|June 13, 2001

Characterization of a novel human opsin gene with wide tissue expression and identification of embedded and flanking genes on chromosome 1q43S Halford, M S Freedman, J Bellingham, et al.

Science (New York, N.Y.)|September 1, 1995

Adaptive evolution of color vision genes in higher primatesS K Shyue, D Hewett-Emmett, H G Sperling, et al.

The British Journal of Ophthalmology|November 12, 2003

Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2)M Michaelides, I A Aligianis, G E Holder, et al.

Human Molecular Genetics|May 1, 1996

Gene transfer into the mouse retina mediated by an adeno-associated viral vectorR R Ali, M B Reichel, A J Thrasher, et al.

The British Journal of Ophthalmology|February 22, 2005

A detailed phenotypic study of "cone dystrophy with supernormal rod ERG"M Michaelides, G E Holder, A R Webster, et al.

Vision Research|January 20, 1999

Molecular evolution of trichromacy in primatesD M Hunt, K S Dulai, J A Cowing, et al.

The British Journal of Ophthalmology|June 19, 2003

Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing lossP J Francis, S Johnson, B Edmunds, et al.

Human Molecular Genetics|January 4, 2001

The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophyR J Newbold, E C Deery, C E Walker, et al.

Cytogenetics and Cell Genetics|January 1, 1994

Localization of the gene encoding human phosphatidylinositol transfer protein (PITPN) to 17p13.3: a gene showing homology to the Drosophila retinal degeneration B gene (rdgB)J Fitzgibbon, A Pilz, S Gayther, et al.

Pageof 15

Showing results (111-120 of 145) with videos related to

Sort By:

Pageof 15

The American Journal of Physiology|May 1, 1991

Abnormal epithelial transport in cystic fibrosis jejunumE V O'Loughlin, D M Hunt, K J Gaskin, et al.

Genomics|June 13, 2001

Characterization of a novel human opsin gene with wide tissue expression and identification of embedded and flanking genes on chromosome 1q43S Halford, M S Freedman, J Bellingham, et al.

Science (New York, N.Y.)|September 1, 1995

Adaptive evolution of color vision genes in higher primatesS K Shyue, D Hewett-Emmett, H G Sperling, et al.

The British Journal of Ophthalmology|November 12, 2003

Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2)M Michaelides, I A Aligianis, G E Holder, et al.

Human Molecular Genetics|May 1, 1996

Gene transfer into the mouse retina mediated by an adeno-associated viral vectorR R Ali, M B Reichel, A J Thrasher, et al.

The British Journal of Ophthalmology|February 22, 2005

A detailed phenotypic study of "cone dystrophy with supernormal rod ERG"M Michaelides, G E Holder, A R Webster, et al.

Vision Research|January 20, 1999

Molecular evolution of trichromacy in primatesD M Hunt, K S Dulai, J A Cowing, et al.

The British Journal of Ophthalmology|June 19, 2003

Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing lossP J Francis, S Johnson, B Edmunds, et al.

Human Molecular Genetics|January 4, 2001

The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophyR J Newbold, E C Deery, C E Walker, et al.

Cytogenetics and Cell Genetics|January 1, 1994

Localization of the gene encoding human phosphatidylinositol transfer protein (PITPN) to 17p13.3: a gene showing homology to the Drosophila retinal degeneration B gene (rdgB)J Fitzgibbon, A Pilz, S Gayther, et al.

Pageof 15