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J Nathans

Showing results (41-50 of 100) with videos related to

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Human Molecular Genetics|April 1, 1995
Rhodopsin mutation proline347-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347J P Macke, J C Hennessey, J Nathans
The Journal of Biological Chemistry|December 15, 1993
Rhodopsin mutations responsible for autosomal dominant retinitis pigmentosa. Clustering of functional classes along the polypeptide chainC H Sung, C M Davenport, J Nathans
Mechanisms of Development|July 25, 2000
Expression and regulation of chicken fibroblast growth factor homologous factor (FHF)-4 at the base of the developing limbsI Muñoz-Sanjuán, J F Fallon, J Nathans
American Journal of Human Genetics|August 1, 1992
Human tritanopia associated with a third amino acid substitution in the blue-sensitive visual pigmentC J Weitz, L N Went, J Nathans
Methods in Enzymology|May 9, 2000
Spectral sensitivities of human cone visual pigments determined in vivo and in vitroA Stockman, L T Sharpe, S Merbs, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 1, 1994
A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segmentC H Sung, C Makino, D Baylor, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999
Biochemical characterization of Wnt-frizzled interactions using a soluble, biologically active vertebrate Wnt proteinJ C Hsieh, A Rattner, P M Smallwood, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 27, 2001
Progressive cerebellar, auditory, and esophageal dysfunction caused by targeted disruption of the frizzled-4 geneY Wang, D Huso, H Cahill, et al.
Genomics|May 15, 1994
Murine and bovine blue cone pigment genes: cloning and characterization of two new members of the S family of visual pigmentsM I Chiu, D J Zack, Y Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1994
Apoptotic photoreceptor cell death in mouse models of retinitis pigmentosaC Portera-Cailliau, C H Sung, J Nathans, et al.
Pageof 10

Showing results (41-50 of 100) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|April 1, 1995
Rhodopsin mutation proline347-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347J P Macke, J C Hennessey, J Nathans
The Journal of Biological Chemistry|December 15, 1993
Rhodopsin mutations responsible for autosomal dominant retinitis pigmentosa. Clustering of functional classes along the polypeptide chainC H Sung, C M Davenport, J Nathans
Mechanisms of Development|July 25, 2000
Expression and regulation of chicken fibroblast growth factor homologous factor (FHF)-4 at the base of the developing limbsI Muñoz-Sanjuán, J F Fallon, J Nathans
American Journal of Human Genetics|August 1, 1992
Human tritanopia associated with a third amino acid substitution in the blue-sensitive visual pigmentC J Weitz, L N Went, J Nathans
Methods in Enzymology|May 9, 2000
Spectral sensitivities of human cone visual pigments determined in vivo and in vitroA Stockman, L T Sharpe, S Merbs, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 1, 1994
A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segmentC H Sung, C Makino, D Baylor, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999
Biochemical characterization of Wnt-frizzled interactions using a soluble, biologically active vertebrate Wnt proteinJ C Hsieh, A Rattner, P M Smallwood, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 27, 2001
Progressive cerebellar, auditory, and esophageal dysfunction caused by targeted disruption of the frizzled-4 geneY Wang, D Huso, H Cahill, et al.
Genomics|May 15, 1994
Murine and bovine blue cone pigment genes: cloning and characterization of two new members of the S family of visual pigmentsM I Chiu, D J Zack, Y Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1994
Apoptotic photoreceptor cell death in mouse models of retinitis pigmentosaC Portera-Cailliau, C H Sung, J Nathans, et al.
Pageof 10