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Y Isashiki

Showing results (21-30 of 40) with videos related to

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American Journal of Ophthalmology|December 22, 2000
Genetic association of manganese superoxide dismutase with exudative age-related macular degenerationK Kimura, Y Isashiki, S Sonoda, et al.
Japanese Journal of Ophthalmology|January 1, 1989
Pigmentary retinal degeneration in patients with HTLV-I-associated myelopathyK Nakao, N Ohba, M Isashiki, et al.
American Journal of Ophthalmology|October 8, 1999
A novel truncating mutation of cytochrome P4501B1 (CYP1B1) gene in primary infantile glaucomaT Kakiuchi, Y Isashiki, K Nakao, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 24, 2000
A novel PAX6 gene mutation (P118R) in a family with congenital nystagmus associated with a variant form of aniridiaS Sonoda, Y Isashiki, Y Tabata, et al.
Protein Sequences & Data Analysis|July 1, 1989
Identification of essential arginine residue(s) for Mg-ATP binding of human argininosuccinate synthetaseY Isashiki, T Noda, K Kobayashi, et al.
American Journal of Ophthalmology|March 10, 2001
Cytochrome P450 1B1 gene mutations in Japanese patients with primary congenital glaucoma(1)T Kakiuchi-Matsumoto, Y Isashiki, N Ohba, et al.
Acta Neurologica Scandinavica|July 1, 1995
Familial mitochondrial encephalomyopathy with deaf-mutism, ophthalmoplegia and leukodystrophyM Nakagawa, Y Kaminishi, Y Isashiki, et al.
Japanese Journal of Ophthalmology|January 1, 1994
Clinical features of HTLV-I associated uveitis determined in multicenter collaborative study. Study Group for HTLV-I Associated Ocular DiseasesN Ohba, K Nakao, Y Isashiki, et al.
Japanese Journal of Ophthalmology|January 1, 1996
Assessment of mitochondrial gene in proliferative vitreoretinal tissues from patients with familial diabetes mellitusY Isashiki, N Ohba, N Hokita, et al.
Human Genetics|January 1, 1995
Novel mutation at the initiation codon in the Norrie disease gene in two Japanese familiesY Isashiki, N Ohba, T Yanagita, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
American Journal of Ophthalmology|December 22, 2000
Genetic association of manganese superoxide dismutase with exudative age-related macular degenerationK Kimura, Y Isashiki, S Sonoda, et al.
Japanese Journal of Ophthalmology|January 1, 1989
Pigmentary retinal degeneration in patients with HTLV-I-associated myelopathyK Nakao, N Ohba, M Isashiki, et al.
American Journal of Ophthalmology|October 8, 1999
A novel truncating mutation of cytochrome P4501B1 (CYP1B1) gene in primary infantile glaucomaT Kakiuchi, Y Isashiki, K Nakao, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 24, 2000
A novel PAX6 gene mutation (P118R) in a family with congenital nystagmus associated with a variant form of aniridiaS Sonoda, Y Isashiki, Y Tabata, et al.
Protein Sequences & Data Analysis|July 1, 1989
Identification of essential arginine residue(s) for Mg-ATP binding of human argininosuccinate synthetaseY Isashiki, T Noda, K Kobayashi, et al.
American Journal of Ophthalmology|March 10, 2001
Cytochrome P450 1B1 gene mutations in Japanese patients with primary congenital glaucoma(1)T Kakiuchi-Matsumoto, Y Isashiki, N Ohba, et al.
Acta Neurologica Scandinavica|July 1, 1995
Familial mitochondrial encephalomyopathy with deaf-mutism, ophthalmoplegia and leukodystrophyM Nakagawa, Y Kaminishi, Y Isashiki, et al.
Japanese Journal of Ophthalmology|January 1, 1994
Clinical features of HTLV-I associated uveitis determined in multicenter collaborative study. Study Group for HTLV-I Associated Ocular DiseasesN Ohba, K Nakao, Y Isashiki, et al.
Japanese Journal of Ophthalmology|January 1, 1996
Assessment of mitochondrial gene in proliferative vitreoretinal tissues from patients with familial diabetes mellitusY Isashiki, N Ohba, N Hokita, et al.
Human Genetics|January 1, 1995
Novel mutation at the initiation codon in the Norrie disease gene in two Japanese familiesY Isashiki, N Ohba, T Yanagita, et al.
Pageof 4