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Experimental Lung Research
|
May 17, 2000
Presence and quantification of neuropeptide Y in pulmonary edema fluids in rats
O Hamdy, K Nishiwaki, M Yajima, et al.
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan
|
August 1, 1991
[Studies on cardiac ingredients of plants. VIII. Preparation of nitrates of proscillaridin and their pharmacological activities]
N Murakami, Y Sato, T Tanase, 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 gene
T Shiono, Y Hotta, M Noro, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 1988
Expression defect of ornithine aminotransferase gene in gyrate atrophy
G Inana, Y Hotta, C Zintz, et al.
Ophthalmic Genetics
|
October 16, 1999
Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy
M 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 pigmentosa
K Fujiki, Y Hotta, A Murakami, et al.
Gifu Shika Gakkai Zasshi = the Journal of Gifu Dental Society
|
June 1, 1989
[Clinical evaluation of synthetic hydroxyapatite implants for human periodontal osseous defects. 6 cases studied more than 3 years after the surgery]
Y Hotta, T Kajimoto, Y Murahashi, et al.
The Japanese Journal of Antibiotics
|
March 1, 1987
[Combined clinical effect of amikacin and cefoxitin in patients with severe infections complicated by hematological diseases]
N Uno, T Nosaka, S Uchiyama, et al.
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 neuropathy
K Fujiki, Y Hotta, M Hayakawa, et al.
Page
of 21
Search research articles
Search
Showing results (181-190 of 209) with videos related to
Sort By:
Page
of 21
Experimental Lung Research
|
May 17, 2000
Presence and quantification of neuropeptide Y in pulmonary edema fluids in rats
O Hamdy, K Nishiwaki, M Yajima, et al.
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan
|
August 1, 1991
[Studies on cardiac ingredients of plants. VIII. Preparation of nitrates of proscillaridin and their pharmacological activities]
N Murakami, Y Sato, T Tanase, 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 gene
T Shiono, Y Hotta, M Noro, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 1988
Expression defect of ornithine aminotransferase gene in gyrate atrophy
G Inana, Y Hotta, C Zintz, et al.
Ophthalmic Genetics
|
October 16, 1999
Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy
M 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 pigmentosa
K Fujiki, Y Hotta, A Murakami, et al.
Gifu Shika Gakkai Zasshi = the Journal of Gifu Dental Society
|
June 1, 1989
[Clinical evaluation of synthetic hydroxyapatite implants for human periodontal osseous defects. 6 cases studied more than 3 years after the surgery]
Y Hotta, T Kajimoto, Y Murahashi, et al.
The Japanese Journal of Antibiotics
|
March 1, 1987
[Combined clinical effect of amikacin and cefoxitin in patients with severe infections complicated by hematological diseases]
N Uno, T Nosaka, S Uchiyama, et al.
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 neuropathy
K Fujiki, Y Hotta, M Hayakawa, et al.
Page
of 21