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K Fujiki

Showing results (41-50 of 89) with videos related to

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American Journal of Ophthalmology|February 15, 1993
Clinical features of autosomal dominant retinitis pigmentosa with rhodopsin gene codon 17 mutation and retinal neovascularization in a Japanese patientM Hayakawa, Y Hotta, Y Imai, et al.
Human Genetics|November 3, 1998
A new L527R mutation of the betaIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacitiesK Fujiki, Y Hotta, K Nakayasu, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|August 18, 2009
The sex determining loci and sex chromosomes in the family salmonidaeW S Davidson, T-K Huang, K Fujiki, et al.
Biomechanics and Modeling in Mechanobiology|May 16, 2012
The influence of mechanical stimulation on osteoclast localization in the mouse maxilla: bone histomorphometry and finite element analysisK Fujiki, K Aoki, P Marcián, et al.
Japanese Journal of Ophthalmology|August 5, 1998
Analysis of peripherin/RDS gene for Japanese retinal dystrophiesK Fujiki, Y Hotta, M Hayakawa, et al.
Annals of Internal Medicine|March 10, 2001
Improvement in atrophic gastritis and intestinal metaplasia in patients in whom Helicobacter pylori was eradicatedT Ohkusa, K Fujiki, I Takashimizu, et al.
Journal of Medical Virology|July 1, 1995
Prediction of relapses after interferon-alpha therapy by hepatitis C virus RNA in peripheral blood mononuclear cellsS Kusaka, T Okusa, A Araki, et al.
Nippon Ganka Gakkai Zasshi|June 1, 1989
[Statistical analysis of Marfan's syndrome]M Wakita, E Ryu, K Nakayasu, et al.
American Journal of Ophthalmology|September 11, 1999
Leu518Pro mutation of the beta ig-h3 gene causes lattice corneal dystrophy type IS Endo, T H Nguyen, K Fujiki, et al.
Ophthalmic Genetics|March 1, 1996
Analysis of phosducin as a candidate gene for retinopathiesF Ara-Iwata, S G Jacobson, J D Gass, et al.
Pageof 9

Showing results (41-50 of 89) with videos related to

Sort By:
Pageof 9
American Journal of Ophthalmology|February 15, 1993
Clinical features of autosomal dominant retinitis pigmentosa with rhodopsin gene codon 17 mutation and retinal neovascularization in a Japanese patientM Hayakawa, Y Hotta, Y Imai, et al.
Human Genetics|November 3, 1998
A new L527R mutation of the betaIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacitiesK Fujiki, Y Hotta, K Nakayasu, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|August 18, 2009
The sex determining loci and sex chromosomes in the family salmonidaeW S Davidson, T-K Huang, K Fujiki, et al.
Biomechanics and Modeling in Mechanobiology|May 16, 2012
The influence of mechanical stimulation on osteoclast localization in the mouse maxilla: bone histomorphometry and finite element analysisK Fujiki, K Aoki, P Marcián, et al.
Japanese Journal of Ophthalmology|August 5, 1998
Analysis of peripherin/RDS gene for Japanese retinal dystrophiesK Fujiki, Y Hotta, M Hayakawa, et al.
Annals of Internal Medicine|March 10, 2001
Improvement in atrophic gastritis and intestinal metaplasia in patients in whom Helicobacter pylori was eradicatedT Ohkusa, K Fujiki, I Takashimizu, et al.
Journal of Medical Virology|July 1, 1995
Prediction of relapses after interferon-alpha therapy by hepatitis C virus RNA in peripheral blood mononuclear cellsS Kusaka, T Okusa, A Araki, et al.
Nippon Ganka Gakkai Zasshi|June 1, 1989
[Statistical analysis of Marfan's syndrome]M Wakita, E Ryu, K Nakayasu, et al.
American Journal of Ophthalmology|September 11, 1999
Leu518Pro mutation of the beta ig-h3 gene causes lattice corneal dystrophy type IS Endo, T H Nguyen, K Fujiki, et al.
Ophthalmic Genetics|March 1, 1996
Analysis of phosducin as a candidate gene for retinopathiesF Ara-Iwata, S G Jacobson, J D Gass, et al.
Pageof 9