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C M Davenport

Showing results (1-10 of 9) with videos related to

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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
Science (New York, N.Y.)|December 22, 1999
Mediation by a CREB family transcription factor of NGF-dependent survival of sympathetic neuronsA Riccio, S Ahn, C M Davenport, et al.
American Journal of Physiology. Cell Physiology|February 15, 2001
Progesterone treatment abolishes exogenously expressed ionic currents in Xenopus oocytesA D Shcherbatko, C M Davenport, J C Speh, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 17, 2020
Loss of Phosphatidylinositol 3-Kinase Activity in Regulatory T Cells Leads to Neuronal InflammationAnne-Katrien Stark, Elizabeth C M Davenport, Daniel T Patton, et al.
Science (New York, N.Y.)|August 25, 1989
Molecular genetics of human blue cone monochromacyJ Nathans, C M Davenport, I H Maumenee, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Rhodopsin mutations in autosomal dominant retinitis pigmentosaC H Sung, C M Davenport, J C Hennessey, et al.
American Journal of Human Genetics|July 1, 1993
Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsinJ P Macke, C M Davenport, S G Jacobson, et al.
Frontiers in Immunology|December 12, 2024
Lack of phosphatidylinositol 3-kinase VPS34 in regulatory T cells leads to a fatal lymphoproliferative disorder without affecting their developmentChristina J F Courreges, Elizabeth C M Davenport, Benoit Bilanges, et al.
Molecular Pharmacology|February 17, 2001
Cloning, expression, and pharmacological characterization of a novel human histamine receptorY Zhu, D Michalovich, H Wu, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
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
Science (New York, N.Y.)|December 22, 1999
Mediation by a CREB family transcription factor of NGF-dependent survival of sympathetic neuronsA Riccio, S Ahn, C M Davenport, et al.
American Journal of Physiology. Cell Physiology|February 15, 2001
Progesterone treatment abolishes exogenously expressed ionic currents in Xenopus oocytesA D Shcherbatko, C M Davenport, J C Speh, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 17, 2020
Loss of Phosphatidylinositol 3-Kinase Activity in Regulatory T Cells Leads to Neuronal InflammationAnne-Katrien Stark, Elizabeth C M Davenport, Daniel T Patton, et al.
Science (New York, N.Y.)|August 25, 1989
Molecular genetics of human blue cone monochromacyJ Nathans, C M Davenport, I H Maumenee, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Rhodopsin mutations in autosomal dominant retinitis pigmentosaC H Sung, C M Davenport, J C Hennessey, et al.
American Journal of Human Genetics|July 1, 1993
Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsinJ P Macke, C M Davenport, S G Jacobson, et al.
Frontiers in Immunology|December 12, 2024
Lack of phosphatidylinositol 3-kinase VPS34 in regulatory T cells leads to a fatal lymphoproliferative disorder without affecting their developmentChristina J F Courreges, Elizabeth C M Davenport, Benoit Bilanges, et al.
Molecular Pharmacology|February 17, 2001
Cloning, expression, and pharmacological characterization of a novel human histamine receptorY Zhu, D Michalovich, H Wu, et al.
Pageof 1