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K Fujiki

Showing results (51-60 of 89) with videos related to

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Journal of Hepato-Biliary-Pancreatic Surgery|September 12, 2000
Adeno-endocrine cell carcinoma of the gallbladderN Eriguchi, S Aoyagi, T Noritomi, et al.
The British Journal of Ophthalmology|May 29, 2003
H626R and R124C mutations of the TGFBI (BIGH3) gene caused lattice corneal dystrophy in Vietnamese peopleH M Chau, N T Ha, L X Cung, et al.
The Kurume Medical Journal|February 5, 2000
A case of Turner's syndrome complicated with desmoid tumor of the transverse colonN Eriguchi, S Aoyagi, K Okuda, et al.
Journal of Human Genetics|December 16, 1998
Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778M Matsumoto, S Hayasaka, Y Hotta, et al.
Fish & Shellfish Immunology|June 23, 2009
Rainbow trout interleukin-2: cloning, expression and bioactivity analysisP Díaz-Rosales, S Bird, T H Wang, et al.
Japanese Journal of Ophthalmology|January 1, 1995
Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNAY Hotta, K Fujiki, M Hayakawa, et al.
Nippon Ganka Gakkai Zasshi|October 1, 1995
[A study on the rhodopsin gene in Japanese retinitis pigmentosa--screening of mutation by restriction endonucreases and frequencies of DNA polymorphisms]H Kawano, Y Hotta, K Fujiki, et al.
Japanese Journal of Ophthalmology|January 1, 1992
Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin geneT Shiono, Y Hotta, M Noro, et al.
Experimental Eye Research|March 1, 1996
Studies on the mechanism of early onset macular degeneration in cynomolgus (Macaca fascicularis) monkeys. I. Abnormal concentrations of two proteins in the retinaM G Nicolas, K Fujiki, K Murayama, et al.
Japanese Journal of Ophthalmology|January 1, 1993
A multicenter study of typical retinitis pigmentosa in JapanM Hayakawa, M Matsumura, N Ohba, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
Journal of Hepato-Biliary-Pancreatic Surgery|September 12, 2000
Adeno-endocrine cell carcinoma of the gallbladderN Eriguchi, S Aoyagi, T Noritomi, et al.
The British Journal of Ophthalmology|May 29, 2003
H626R and R124C mutations of the TGFBI (BIGH3) gene caused lattice corneal dystrophy in Vietnamese peopleH M Chau, N T Ha, L X Cung, et al.
The Kurume Medical Journal|February 5, 2000
A case of Turner's syndrome complicated with desmoid tumor of the transverse colonN Eriguchi, S Aoyagi, K Okuda, et al.
Journal of Human Genetics|December 16, 1998
Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778M Matsumoto, S Hayasaka, Y Hotta, et al.
Fish & Shellfish Immunology|June 23, 2009
Rainbow trout interleukin-2: cloning, expression and bioactivity analysisP Díaz-Rosales, S Bird, T H Wang, et al.
Japanese Journal of Ophthalmology|January 1, 1995
Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNAY Hotta, K Fujiki, M Hayakawa, et al.
Nippon Ganka Gakkai Zasshi|October 1, 1995
[A study on the rhodopsin gene in Japanese retinitis pigmentosa--screening of mutation by restriction endonucreases and frequencies of DNA polymorphisms]H Kawano, Y Hotta, K Fujiki, et al.
Japanese Journal of Ophthalmology|January 1, 1992
Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin geneT Shiono, Y Hotta, M Noro, et al.
Experimental Eye Research|March 1, 1996
Studies on the mechanism of early onset macular degeneration in cynomolgus (Macaca fascicularis) monkeys. I. Abnormal concentrations of two proteins in the retinaM G Nicolas, K Fujiki, K Murayama, et al.
Japanese Journal of Ophthalmology|January 1, 1993
A multicenter study of typical retinitis pigmentosa in JapanM Hayakawa, M Matsumura, N Ohba, et al.
Pageof 9