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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 neuropathy
M 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 library
Y 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 mitochondria
Y 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 death
W 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 healing
T 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 disease
Y Hotta, M Hayakawa, H Kawano, et al.
Human Genetics
|
October 6, 1998
Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene
Y Hotta, K Fujiki, M Hayakawa, et al.
Ophthalmic Research
|
March 4, 1998
Visual function in retinitis pigmentosa related to a codon 15 rhodopsin gene mutation
M 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 stress
M G Nicolas, K Fujiki, K Murayama, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 209) with videos related to
Sort By:
Page
of 21
Japanese Journal of Ophthalmology
|
January 1, 1992
High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy
M 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 library
Y 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 mitochondria
Y 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 death
W 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 healing
T 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 disease
Y Hotta, M Hayakawa, H Kawano, et al.
Human Genetics
|
October 6, 1998
Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene
Y Hotta, K Fujiki, M Hayakawa, et al.
Ophthalmic Research
|
March 4, 1998
Visual function in retinitis pigmentosa related to a codon 15 rhodopsin gene mutation
M 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 stress
M G Nicolas, K Fujiki, K Murayama, et al.
Page
of 21