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American Journal of Physiology. Cell Physiology
|
March 14, 2001
Ontogenetic, gravity-dependent development of rat soleus muscle
Y Ohira, T Tanaka, T Yoshinaga, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 1992
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts
A Chomyn, A Martinuzzi, M Yoneda, et al.
Journal of the Neurological Sciences
|
September 12, 2000
Walker-Warburg syndrome is genetically distinct from Fukuyama type congenital muscular dystrophy
Y Chadani, T Kondoh, N Kamimura, et al.
Biochemical and Biophysical Research Communications
|
September 15, 1994
Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle
Y Mizuno, S Noguchi, H Yamamoto, et al.
Brain & Development
|
December 5, 2000
A case of Walker-Warburg syndrome
Y Asano, K Minagawa, A Okuda, et al.
Neuromuscular Disorders : NMD
|
April 12, 2001
A case of MERRF associated with chronic pancreatitis
M Toyono, K Nakano, M Kiuchi, et al.
American Journal of Medical Genetics
|
March 21, 1998
Muscular dystrophy associated with extra-abdominal desmoid tumor showing aberrant chromosome 1 [46,XX,add(1)(p36)]
M Katsuura, M Kato, D Sendo, et al.
Muscle & Nerve
|
May 8, 1998
Mitochondrial abnormalities in selenium-deficient myopathy
Y Osaki, I Nishino, N Murakami, et al.
Immunobiology
|
December 4, 2014
Epididymal C4b-binding protein is processed and degraded during transit through the duct and is not essential for fertility
Mayumi I Nonaka, Eva Zsigmond, Akihiko Kudo, et al.
Neuropediatrics
|
November 1, 1982
Vacuolar myopathy with type 2 A fiber atrophy and type 2 B fiber deficiency. A case of childhood form acid alpha-1,4-glucosidase deficiency
T Matsuishi, K Terasawa, I Yoshida, et al.
Page
of 51
Search research articles
Search
Showing results (461-470 of 503) with videos related to
Sort By:
Page
of 51
American Journal of Physiology. Cell Physiology
|
March 14, 2001
Ontogenetic, gravity-dependent development of rat soleus muscle
Y Ohira, T Tanaka, T Yoshinaga, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 1992
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts
A Chomyn, A Martinuzzi, M Yoneda, et al.
Journal of the Neurological Sciences
|
September 12, 2000
Walker-Warburg syndrome is genetically distinct from Fukuyama type congenital muscular dystrophy
Y Chadani, T Kondoh, N Kamimura, et al.
Biochemical and Biophysical Research Communications
|
September 15, 1994
Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle
Y Mizuno, S Noguchi, H Yamamoto, et al.
Brain & Development
|
December 5, 2000
A case of Walker-Warburg syndrome
Y Asano, K Minagawa, A Okuda, et al.
Neuromuscular Disorders : NMD
|
April 12, 2001
A case of MERRF associated with chronic pancreatitis
M Toyono, K Nakano, M Kiuchi, et al.
American Journal of Medical Genetics
|
March 21, 1998
Muscular dystrophy associated with extra-abdominal desmoid tumor showing aberrant chromosome 1 [46,XX,add(1)(p36)]
M Katsuura, M Kato, D Sendo, et al.
Muscle & Nerve
|
May 8, 1998
Mitochondrial abnormalities in selenium-deficient myopathy
Y Osaki, I Nishino, N Murakami, et al.
Immunobiology
|
December 4, 2014
Epididymal C4b-binding protein is processed and degraded during transit through the duct and is not essential for fertility
Mayumi I Nonaka, Eva Zsigmond, Akihiko Kudo, et al.
Neuropediatrics
|
November 1, 1982
Vacuolar myopathy with type 2 A fiber atrophy and type 2 B fiber deficiency. A case of childhood form acid alpha-1,4-glucosidase deficiency
T Matsuishi, K Terasawa, I Yoshida, et al.
Page
of 51