Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

K Fujiki

Showing results (61-70 of 89) with videos related to

Pageof 9
Sort By:
Nippon Ganka Gakkai Zasshi|February 1, 1992
[Molecular biological study of the rhodopsin gene in Japanese patients with autosomal dominant retinitis pigmentosa]Y Hotta, T Shiono, M Hayakawa, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|June 1, 1991
A mutation of mitochondrial DNA in Japanese families with Leber's hereditary optic neuropathyK Fujiki, Y Hotta, M Hayakawa, et al.
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 Kurume Medical Journal|July 20, 1999
Endocrine tumor of the pancreas--an evaluation of eighteen patients who underwent resection followed by long-term survivalN Eriguchi, S Aoyagi, H Imayama, et al.
Ophthalmic Genetics|October 16, 1999
Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathyM Matsumoto, S Hayasaka, C Kadoi, et al.
The Japanese Journal of Human Genetics|September 1, 1995
Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosaK Fujiki, Y Hotta, A Murakami, et al.
Nippon Ganka Gakkai Zasshi|February 1, 1992
[An epidemiogenetic study of typical retinitis pigmentosa in Japan--a preliminary report of nationwide, multicenter study]K Fujiki, M Hayakawa, A Kanai, et al.
Journal of Clinical Gastroenterology|December 1, 1991
A high frequency of detection of Helicobacter pylori in whitish exudate of gastric ulcerT Ohkusa, I Okayasu, 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.
International Journal of Clinical Pharmacology Research|December 22, 2005
Methotrexate-induced acute lung injury in a patient with rheumatoid arthritisK Taniguchi, Y Usui, T Matsuda, et al.
Pageof 9

Showing results (61-70 of 89) with videos related to

Sort By:
Pageof 9
Nippon Ganka Gakkai Zasshi|February 1, 1992
[Molecular biological study of the rhodopsin gene in Japanese patients with autosomal dominant retinitis pigmentosa]Y Hotta, T Shiono, M Hayakawa, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|June 1, 1991
A mutation of mitochondrial DNA in Japanese families with Leber's hereditary optic neuropathyK Fujiki, Y Hotta, M Hayakawa, et al.
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 Kurume Medical Journal|July 20, 1999
Endocrine tumor of the pancreas--an evaluation of eighteen patients who underwent resection followed by long-term survivalN Eriguchi, S Aoyagi, H Imayama, et al.
Ophthalmic Genetics|October 16, 1999
Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathyM Matsumoto, S Hayasaka, C Kadoi, et al.
The Japanese Journal of Human Genetics|September 1, 1995
Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosaK Fujiki, Y Hotta, A Murakami, et al.
Nippon Ganka Gakkai Zasshi|February 1, 1992
[An epidemiogenetic study of typical retinitis pigmentosa in Japan--a preliminary report of nationwide, multicenter study]K Fujiki, M Hayakawa, A Kanai, et al.
Journal of Clinical Gastroenterology|December 1, 1991
A high frequency of detection of Helicobacter pylori in whitish exudate of gastric ulcerT Ohkusa, I Okayasu, 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.
International Journal of Clinical Pharmacology Research|December 22, 2005
Methotrexate-induced acute lung injury in a patient with rheumatoid arthritisK Taniguchi, Y Usui, T Matsuda, et al.
Pageof 9