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Darryl Y Nishimura

Showing results (1-10 of 26) with videos related to

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American Journal of Physiology. Renal Physiology|November 26, 2010
Inactivation of Bardet-Biedl syndrome genes causes kidney defectsDeng-Fu Guo, Andreas M Beyer, Baoli Yang, et al.
Investigative Ophthalmology & Visual Science|March 16, 2021
Mitophagy: An Emerging Target in Ocular PathologyJessica M Skeie, Darryl Y Nishimura, Cheryl L Wang, et al.
The Journal of Clinical Investigation|March 5, 2008
Leptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndromeKamal Rahmouni, Melissa A Fath, Seongjin Seo, et al.
Human Mutation|February 2, 2010
Bardet-Biedl syndrome in Denmark--report of 13 novel sequence variations in six genesTina Duelund Hjortshøj, Karen Grønskov, Alisdair R Philp, et al.
Investigative Ophthalmology & Visual Science|June 27, 2007
Gene expression analysis of photoreceptor cell loss in bbs4-knockout mice reveals an early stress gene response and photoreceptor cell damageRuth E Swiderski, Darryl Y Nishimura, Robert F Mullins, et al.
Journal of Glaucoma|February 1, 2002
Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from BrazilAdriana Silva Borges, Remo Susanna, José Carlos Eudes Carani, et al.
Plos Genetics|October 20, 2017
BBSome function is required for both the morphogenesis and maintenance of the photoreceptor outer segmentYing Hsu, Janelle E Garrison, Gunhee Kim, et al.
American Journal of Ophthalmology|March 5, 2003
A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 geneRobert A Honkanen, Darryl Y Nishimura, Ruth E Swiderski, et al.
Journal of Cell Science|January 23, 2019
BBS4 is required for intraflagellar transport coordination and basal body number in mammalian olfactory ciliaCedric R Uytingco, Corey L Williams, Chao Xie, et al.
Cornea|June 20, 2020
Ubiquinol Supplementation of Donor Tissue Enhances Corneal Endothelial Cell Mitochondrial RespirationJessica M Skeie, Benjamin T Aldrich, Darryl Y Nishimura, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
American Journal of Physiology. Renal Physiology|November 26, 2010
Inactivation of Bardet-Biedl syndrome genes causes kidney defectsDeng-Fu Guo, Andreas M Beyer, Baoli Yang, et al.
Investigative Ophthalmology & Visual Science|March 16, 2021
Mitophagy: An Emerging Target in Ocular PathologyJessica M Skeie, Darryl Y Nishimura, Cheryl L Wang, et al.
The Journal of Clinical Investigation|March 5, 2008
Leptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndromeKamal Rahmouni, Melissa A Fath, Seongjin Seo, et al.
Human Mutation|February 2, 2010
Bardet-Biedl syndrome in Denmark--report of 13 novel sequence variations in six genesTina Duelund Hjortshøj, Karen Grønskov, Alisdair R Philp, et al.
Investigative Ophthalmology & Visual Science|June 27, 2007
Gene expression analysis of photoreceptor cell loss in bbs4-knockout mice reveals an early stress gene response and photoreceptor cell damageRuth E Swiderski, Darryl Y Nishimura, Robert F Mullins, et al.
Journal of Glaucoma|February 1, 2002
Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from BrazilAdriana Silva Borges, Remo Susanna, José Carlos Eudes Carani, et al.
Plos Genetics|October 20, 2017
BBSome function is required for both the morphogenesis and maintenance of the photoreceptor outer segmentYing Hsu, Janelle E Garrison, Gunhee Kim, et al.
American Journal of Ophthalmology|March 5, 2003
A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 geneRobert A Honkanen, Darryl Y Nishimura, Ruth E Swiderski, et al.
Journal of Cell Science|January 23, 2019
BBS4 is required for intraflagellar transport coordination and basal body number in mammalian olfactory ciliaCedric R Uytingco, Corey L Williams, Chao Xie, et al.
Cornea|June 20, 2020
Ubiquinol Supplementation of Donor Tissue Enhances Corneal Endothelial Cell Mitochondrial RespirationJessica M Skeie, Benjamin T Aldrich, Darryl Y Nishimura, et al.
Pageof 3