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Biological & Pharmaceutical Bulletin
|
January 5, 2002
Antiproliferative constituents in the plant 8. Seeds of Rhynchosia volubilis
J Kinjo, S Nagao, T Tanaka, et al.
Muscle & Nerve
|
November 1, 1992
An experimental model of mitochondrial myopathy: germanium-induced myopathy and coenzyme Q10 administration
C M Wu, T Matsuoka, M Takemitsu, et al.
Muscle & Nerve
|
November 1, 1991
Muscle histology in Becker muscular dystrophy
M Kaido, K Arahata, E P Hoffman, et al.
Molecular Biology and Evolution
|
May 27, 2011
Retained orthologous relationships of the MHC Class I genes during euteleost evolution
Mayumi I Nonaka, Kouichi Aizawa, Hiroshi Mitani, et al.
No to Hattatsu = Brain and Development
|
March 21, 2000
[A case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)]
M Tojo, T Gunji, S Yamaguchi, et al.
Journal of Biochemistry
|
July 1, 1983
Immunocytochemical localization of cathepsin B in degenerating rat skeletal muscle induced by a local anesthetic, bupivacaine
S Ishiura, I Nonaka, H Nakase, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes
S Mita, M Tokunaga, T Kumamoto, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 30, 1995
Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation
H Sugie, Y Sugie, M Ito, et al.
Brain & Development
|
January 1, 1996
Long-term therapy with cytochrome c, flavin mononucleotide and thiamine diphosphate for a patient with Kearns-Sayre syndrome
E Nakagawa, S Osari, H Yamanouchi, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
February 1, 1994
[Dystrophin-related protein in diaphragm, limb and myoblast transferred muscles of mdx mouse]
M Takemitsu, R Koga, S Ishiura, et al.
Page
of 51
Search research articles
Search
Showing results (251-260 of 503) with videos related to
Sort By:
Page
of 51
Biological & Pharmaceutical Bulletin
|
January 5, 2002
Antiproliferative constituents in the plant 8. Seeds of Rhynchosia volubilis
J Kinjo, S Nagao, T Tanaka, et al.
Muscle & Nerve
|
November 1, 1992
An experimental model of mitochondrial myopathy: germanium-induced myopathy and coenzyme Q10 administration
C M Wu, T Matsuoka, M Takemitsu, et al.
Muscle & Nerve
|
November 1, 1991
Muscle histology in Becker muscular dystrophy
M Kaido, K Arahata, E P Hoffman, et al.
Molecular Biology and Evolution
|
May 27, 2011
Retained orthologous relationships of the MHC Class I genes during euteleost evolution
Mayumi I Nonaka, Kouichi Aizawa, Hiroshi Mitani, et al.
No to Hattatsu = Brain and Development
|
March 21, 2000
[A case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)]
M Tojo, T Gunji, S Yamaguchi, et al.
Journal of Biochemistry
|
July 1, 1983
Immunocytochemical localization of cathepsin B in degenerating rat skeletal muscle induced by a local anesthetic, bupivacaine
S Ishiura, I Nonaka, H Nakase, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes
S Mita, M Tokunaga, T Kumamoto, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 30, 1995
Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation
H Sugie, Y Sugie, M Ito, et al.
Brain & Development
|
January 1, 1996
Long-term therapy with cytochrome c, flavin mononucleotide and thiamine diphosphate for a patient with Kearns-Sayre syndrome
E Nakagawa, S Osari, H Yamanouchi, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
February 1, 1994
[Dystrophin-related protein in diaphragm, limb and myoblast transferred muscles of mdx mouse]
M Takemitsu, R Koga, S Ishiura, et al.
Page
of 51