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James S Friedman

Showing results (1-10 of 15) with videos related to

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Human Mutation|March 6, 2007
Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activityAtsuhiro Kanda, James S Friedman, Koji M Nishiguchi, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 16, 2010
Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 geneTherése Hugosson, James S Friedman, Vesna Ponjavic, et al.
Human Genomics|May 17, 2013
Update on the Kelch-like (KLHL) gene familyBajinder S Dhanoa, Tiziana Cogliati, Akhila G Satish, et al.
The Journal of Biological Chemistry|July 21, 2006
Retinoic acid regulates the expression of photoreceptor transcription factor NRLHemant Khanna, Masayuki Akimoto, Sandrine Siffroi-Fernandez, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2004
Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone functionKoji M Nishiguchi, James S Friedman, Michael A Sandberg, et al.
The Journal of Biological Chemistry|August 5, 2004
Altered expression of genes of the Bmp/Smad and Wnt/calcium signaling pathways in the cone-only Nrl-/- mouse retina, revealed by gene profiling using custom cDNA microarraysJindan Yu, Shirley He, James S Friedman, et al.
Human Molecular Genetics|May 23, 2002
Protein localization in the human eye and genetic screen of opticinJames S Friedman, Mathieu Faucher, Paul Hiscott, et al.
The Journal of Biological Chemistry|August 26, 2004
The minimal transactivation domain of the basic motif-leucine zipper transcription factor NRL interacts with TATA-binding proteinJames S Friedman, Hemant Khanna, Prabodh K Swain, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 9, 2009
Canine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3Anna V Kukekova, Orly Goldstein, Jennifer L Johnson, et al.
Human Molecular Genetics|May 28, 2004
Expression profiling of the developing and mature Nrl-/- mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of NrlShigeo Yoshida, Alan J Mears, James S Friedman, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Human Mutation|March 6, 2007
Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activityAtsuhiro Kanda, James S Friedman, Koji M Nishiguchi, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 16, 2010
Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 geneTherése Hugosson, James S Friedman, Vesna Ponjavic, et al.
Human Genomics|May 17, 2013
Update on the Kelch-like (KLHL) gene familyBajinder S Dhanoa, Tiziana Cogliati, Akhila G Satish, et al.
The Journal of Biological Chemistry|July 21, 2006
Retinoic acid regulates the expression of photoreceptor transcription factor NRLHemant Khanna, Masayuki Akimoto, Sandrine Siffroi-Fernandez, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2004
Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone functionKoji M Nishiguchi, James S Friedman, Michael A Sandberg, et al.
The Journal of Biological Chemistry|August 5, 2004
Altered expression of genes of the Bmp/Smad and Wnt/calcium signaling pathways in the cone-only Nrl-/- mouse retina, revealed by gene profiling using custom cDNA microarraysJindan Yu, Shirley He, James S Friedman, et al.
Human Molecular Genetics|May 23, 2002
Protein localization in the human eye and genetic screen of opticinJames S Friedman, Mathieu Faucher, Paul Hiscott, et al.
The Journal of Biological Chemistry|August 26, 2004
The minimal transactivation domain of the basic motif-leucine zipper transcription factor NRL interacts with TATA-binding proteinJames S Friedman, Hemant Khanna, Prabodh K Swain, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 9, 2009
Canine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3Anna V Kukekova, Orly Goldstein, Jennifer L Johnson, et al.
Human Molecular Genetics|May 28, 2004
Expression profiling of the developing and mature Nrl-/- mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of NrlShigeo Yoshida, Alan J Mears, James S Friedman, et al.
Pageof 2