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Acta Neuropathologica
|
January 1, 1995
Dystrophin-positive muscle fibers following C2 myoblast transplantation into mdx nude mice
Y Hagiwara, Y Mizuno, M Takemitsu, et al.
Journal of Biochemistry
|
January 1, 1994
Expression of dystrophin-associated protein 35DAG (A4) and 50DAG (A2) is confined to striated muscles
H Yamamoto, Y Mizuno, K Hayashi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 24, 2008
Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients
R M El Sherif, N Aly Fahmy, I Nonaka, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1991
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
J Hayashi, S Ohta, A Kikuchi, et al.
Journal of the American Academy of Dermatology
|
January 1, 1988
Intraepidermal pilar epithelioma: a new dermatopathologic interpretation of a skin tumor
M Ito, T Tazawa, N Shimizu, et al.
Neuromuscular Disorders : NMD
|
November 1, 1995
The 8,344 mutation in mitochondrial DNA: a comparison between the proportion of mutant DNA and clinico-pathologic findings
M Ozawa, Y Goto, R Sakuta, et al.
No to Hattatsu = Brain and Development
|
September 1, 1993
[A patient with lysosomal glycogen storage disease with normal acid maltase]
M Itoh, Y Asano, M Shimohira, et al.
Journal of Child Neurology
|
February 1, 1997
Recurrent muscle weakness and ataxia in thiamine-responsive pyruvate dehydrogenase complex deficiency
H Kinoshita, N Sakuragawa, H Tada, et al.
Neuropediatrics
|
August 1, 1981
A clinical and histological study of Ullrich's disease (congenital atonic-sclerotic muscular dystrophy)
I Nonaka, Y Une, T Ishihara, et al.
Journal of Inherited Metabolic Disease
|
November 5, 1997
The association between haematological manifestation and mtDNA deletions in Pearson syndrome
K Muraki, S Nishimura, Y Goto, et al.
Page
of 51
Search research articles
Search
Showing results (271-280 of 503) with videos related to
Sort By:
Page
of 51
Acta Neuropathologica
|
January 1, 1995
Dystrophin-positive muscle fibers following C2 myoblast transplantation into mdx nude mice
Y Hagiwara, Y Mizuno, M Takemitsu, et al.
Journal of Biochemistry
|
January 1, 1994
Expression of dystrophin-associated protein 35DAG (A4) and 50DAG (A2) is confined to striated muscles
H Yamamoto, Y Mizuno, K Hayashi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 24, 2008
Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients
R M El Sherif, N Aly Fahmy, I Nonaka, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1991
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
J Hayashi, S Ohta, A Kikuchi, et al.
Journal of the American Academy of Dermatology
|
January 1, 1988
Intraepidermal pilar epithelioma: a new dermatopathologic interpretation of a skin tumor
M Ito, T Tazawa, N Shimizu, et al.
Neuromuscular Disorders : NMD
|
November 1, 1995
The 8,344 mutation in mitochondrial DNA: a comparison between the proportion of mutant DNA and clinico-pathologic findings
M Ozawa, Y Goto, R Sakuta, et al.
No to Hattatsu = Brain and Development
|
September 1, 1993
[A patient with lysosomal glycogen storage disease with normal acid maltase]
M Itoh, Y Asano, M Shimohira, et al.
Journal of Child Neurology
|
February 1, 1997
Recurrent muscle weakness and ataxia in thiamine-responsive pyruvate dehydrogenase complex deficiency
H Kinoshita, N Sakuragawa, H Tada, et al.
Neuropediatrics
|
August 1, 1981
A clinical and histological study of Ullrich's disease (congenital atonic-sclerotic muscular dystrophy)
I Nonaka, Y Une, T Ishihara, et al.
Journal of Inherited Metabolic Disease
|
November 5, 1997
The association between haematological manifestation and mtDNA deletions in Pearson syndrome
K Muraki, S Nishimura, Y Goto, et al.
Page
of 51