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Ophthalmic Genetics
|
March 1, 1996
Analysis of phosducin as a candidate gene for retinopathies
F Ara-Iwata, S G Jacobson, J D Gass, et al.
The Journal of Pediatrics
|
February 1, 1987
Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome
M Kobayashi, H Morishita, N Sugiyama, et al.
Clinical Nutrition (Edinburgh, Scotland)
|
November 17, 2016
Nutritional assessment using stable isotope ratios of carbon and nitrogen in the scalp hair of geriatric patients who received enteral and parenteral nutrition formulas
M Hayasaka, H Ogasawara, Y Hotta, 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 11,778
M Matsumoto, S Hayasaka, Y Hotta, et al.
Chemical & Pharmaceutical Bulletin
|
August 1, 1991
Studies on cardiac ingredients of plants. VII: Chemical transformation of proscillaridin by means of the Diels-Alder reaction and biological activities of its derivatives
N Murakami, T Tanase, S Nagai, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
March 1, 1994
cDNA cloning and functional characterization of a meiosis-specific protein (MNS1) with apparent nuclear association
K Furukawa, H Inagaki, T Naruge, et al.
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan
|
November 1, 1992
[Studies on cardiac ingredients of plants. X. Preparation of nitrates of tetrahydroproscillaridin and their pharmacological activities]
T Tanase, N Murakami, A Nagatsu, et al.
Diabetes Research and Clinical Practice
|
November 5, 1997
The level of erythrocyte aldose reductase is associated with the severity of diabetic retinopathy
C Nishimura, Y Hotta, T Gui, et al.
Japanese Journal of Ophthalmology
|
January 1, 1995
Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA
Y 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.
Page
of 21
Search research articles
Search
Showing results (171-180 of 209) with videos related to
Sort By:
Page
of 21
Ophthalmic Genetics
|
March 1, 1996
Analysis of phosducin as a candidate gene for retinopathies
F Ara-Iwata, S G Jacobson, J D Gass, et al.
The Journal of Pediatrics
|
February 1, 1987
Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome
M Kobayashi, H Morishita, N Sugiyama, et al.
Clinical Nutrition (Edinburgh, Scotland)
|
November 17, 2016
Nutritional assessment using stable isotope ratios of carbon and nitrogen in the scalp hair of geriatric patients who received enteral and parenteral nutrition formulas
M Hayasaka, H Ogasawara, Y Hotta, 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 11,778
M Matsumoto, S Hayasaka, Y Hotta, et al.
Chemical & Pharmaceutical Bulletin
|
August 1, 1991
Studies on cardiac ingredients of plants. VII: Chemical transformation of proscillaridin by means of the Diels-Alder reaction and biological activities of its derivatives
N Murakami, T Tanase, S Nagai, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
March 1, 1994
cDNA cloning and functional characterization of a meiosis-specific protein (MNS1) with apparent nuclear association
K Furukawa, H Inagaki, T Naruge, et al.
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan
|
November 1, 1992
[Studies on cardiac ingredients of plants. X. Preparation of nitrates of tetrahydroproscillaridin and their pharmacological activities]
T Tanase, N Murakami, A Nagatsu, et al.
Diabetes Research and Clinical Practice
|
November 5, 1997
The level of erythrocyte aldose reductase is associated with the severity of diabetic retinopathy
C Nishimura, Y Hotta, T Gui, et al.
Japanese Journal of Ophthalmology
|
January 1, 1995
Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA
Y 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.
Page
of 21