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Y Hotta

Showing results (191-200 of 209) with videos related to

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Japanese Journal of Ophthalmology|January 1, 1992
High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathyM Nakamura, F Ara, M Yamada, et al.
The Japanese Journal of Human Genetics|June 1, 1992
Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP)K Fujiki, Y Hotta, M Hayakawa, et al.
Japanese Journal of Ophthalmology|March 24, 1998
Plus/minus screening of rabbit corneal endothelial cDNA libraryY Hotta, H Kitagawa, K Fujiki, et al.
European Journal of Pharmacology|October 8, 1999
Protective role of nitric oxide synthase against ischemia-reperfusion injury in guinea pig myocardial mitochondriaY Hotta, H Otsuka-Murakami, M Fujita, et al.
Journal of Cell Science|February 1, 2000
4-hydroxynonenal induces a cellular redox status-related activation of the caspase cascade for apoptotic cell deathW Liu, M Kato, A A Akhand, et al.
Gene Therapy|August 9, 2003
Coxsackievirus and adenovirus receptor (CAR)-positive immature osteoblasts as targets of adenovirus-mediated gene transfer for fracture healingT Ito, K Tokunaga, H Maruyama, et al.
Ocular Immunology and Inflammation|July 26, 2012
Analysis of herpes virus group (DNA) from cerebrospinal fluid in vogt-koyanagi-harada diseaseY Hotta, M Hayakawa, H Kawano, et al.
Human Genetics|October 6, 1998
Japanese juvenile retinoschisis is caused by mutations of the XLRS1 geneY Hotta, K Fujiki, M Hayakawa, et al.
Ophthalmic Research|March 4, 1998
Visual function in retinitis pigmentosa related to a codon 15 rhodopsin gene mutationM Yoshii, A Murakami, K Akeo, et al.
Experimental Eye Research|April 1, 1996
Studies on the mechanism of early onset macular degeneration in cynomolgus monkeys. II. Suppression of metallothionein synthesis in the retina in oxidative stressM G Nicolas, K Fujiki, K Murayama, et al.
Pageof 21

Showing results (191-200 of 209) with videos related to

Sort By:
Pageof 21
Japanese Journal of Ophthalmology|January 1, 1992
High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathyM Nakamura, F Ara, M Yamada, et al.
The Japanese Journal of Human Genetics|June 1, 1992
Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP)K Fujiki, Y Hotta, M Hayakawa, et al.
Japanese Journal of Ophthalmology|March 24, 1998
Plus/minus screening of rabbit corneal endothelial cDNA libraryY Hotta, H Kitagawa, K Fujiki, et al.
European Journal of Pharmacology|October 8, 1999
Protective role of nitric oxide synthase against ischemia-reperfusion injury in guinea pig myocardial mitochondriaY Hotta, H Otsuka-Murakami, M Fujita, et al.
Journal of Cell Science|February 1, 2000
4-hydroxynonenal induces a cellular redox status-related activation of the caspase cascade for apoptotic cell deathW Liu, M Kato, A A Akhand, et al.
Gene Therapy|August 9, 2003
Coxsackievirus and adenovirus receptor (CAR)-positive immature osteoblasts as targets of adenovirus-mediated gene transfer for fracture healingT Ito, K Tokunaga, H Maruyama, et al.
Ocular Immunology and Inflammation|July 26, 2012
Analysis of herpes virus group (DNA) from cerebrospinal fluid in vogt-koyanagi-harada diseaseY Hotta, M Hayakawa, H Kawano, et al.
Human Genetics|October 6, 1998
Japanese juvenile retinoschisis is caused by mutations of the XLRS1 geneY Hotta, K Fujiki, M Hayakawa, et al.
Ophthalmic Research|March 4, 1998
Visual function in retinitis pigmentosa related to a codon 15 rhodopsin gene mutationM Yoshii, A Murakami, K Akeo, et al.
Experimental Eye Research|April 1, 1996
Studies on the mechanism of early onset macular degeneration in cynomolgus monkeys. II. Suppression of metallothionein synthesis in the retina in oxidative stressM G Nicolas, K Fujiki, K Murayama, et al.
Pageof 21