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Journal of Dairy Science
|
April 12, 2006
Developmental changes in the kinetics of glucose and urea in Holstein calves
H Hayashi, M Kawai, I Nonaka, et al.
Biochemical and Biophysical Research Communications
|
September 16, 1991
Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patients
Y Tanno, M Yoneda, I Nonaka, et al.
Biochemistry International
|
March 1, 1987
Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies
M Tanaka, M Nishikimi, H Suzuki, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
January 26, 2002
[Adult form of acid maltase deficiency presenting with pattern of muscle weakness resembling facioscapulohumeral dystrophy]
Y Oya, H Morita, M Ogawa, et al.
Journal of the Neurological Sciences
|
December 1, 1987
Muscle fiber growth and necrosis in dystrophic muscles: a comparative study between dy and mdx mice
M Woo, Y Tanabe, H Ishii, et al.
Brain & Development
|
January 1, 1988
Defects in muscle fiber growth in fatal infantile cytochrome c oxidase deficiency
I Nonaka, Y Koga, E Okino, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
September 26, 2000
[Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report]
Y Oya, M Segawa, M Ogawa, et al.
Journal of the Neurological Sciences
|
November 24, 1999
Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan
N Minami, I Nishino, O Kobayashi, et al.
Human Molecular Genetics
|
February 9, 1999
Circular dystrophin RNAs consisting of exons that were skipped by alternative splicing
A Surono, Y Takeshima, T Wibawa, et al.
Journal of Child Neurology
|
April 1, 1993
A T-to-G mutation at nucleotide pair 8993 in mitochondrial DNA in a patient with Leigh's syndrome
H Yoshinaga, T Ogino, S Ohtahara, et al.
Page
of 51
Search research articles
Search
Showing results (261-270 of 503) with videos related to
Sort By:
Page
of 51
Journal of Dairy Science
|
April 12, 2006
Developmental changes in the kinetics of glucose and urea in Holstein calves
H Hayashi, M Kawai, I Nonaka, et al.
Biochemical and Biophysical Research Communications
|
September 16, 1991
Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patients
Y Tanno, M Yoneda, I Nonaka, et al.
Biochemistry International
|
March 1, 1987
Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies
M Tanaka, M Nishikimi, H Suzuki, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
January 26, 2002
[Adult form of acid maltase deficiency presenting with pattern of muscle weakness resembling facioscapulohumeral dystrophy]
Y Oya, H Morita, M Ogawa, et al.
Journal of the Neurological Sciences
|
December 1, 1987
Muscle fiber growth and necrosis in dystrophic muscles: a comparative study between dy and mdx mice
M Woo, Y Tanabe, H Ishii, et al.
Brain & Development
|
January 1, 1988
Defects in muscle fiber growth in fatal infantile cytochrome c oxidase deficiency
I Nonaka, Y Koga, E Okino, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
September 26, 2000
[Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report]
Y Oya, M Segawa, M Ogawa, et al.
Journal of the Neurological Sciences
|
November 24, 1999
Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan
N Minami, I Nishino, O Kobayashi, et al.
Human Molecular Genetics
|
February 9, 1999
Circular dystrophin RNAs consisting of exons that were skipped by alternative splicing
A Surono, Y Takeshima, T Wibawa, et al.
Journal of Child Neurology
|
April 1, 1993
A T-to-G mutation at nucleotide pair 8993 in mitochondrial DNA in a patient with Leigh's syndrome
H Yoshinaga, T Ogino, S Ohtahara, et al.
Page
of 51