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Nature Genetics
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October 4, 2000
Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes
K Inoue, K Nakada, A Ogura, et al.
Muscle & Nerve. Supplement
|
April 12, 2013
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses
K Arahata, T Ishihara, H Fukunaga, et al.
Neuroscience Letters
|
December 31, 1998
Up-regulation of glial cell line-derived neurotrophic factor (GDNF) expression in regenerating muscle fibers in neuromuscular diseases
H Suzuki, A Hase, B Y Kim, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
Presence of emerinopathy in cases of rigid spine syndrome
S Kubo, T Tsukahara, M Takemitsu, et al.
Neurology
|
July 11, 2001
Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy
Y K Hayashi, M Ogawa, K Tagawa, et al.
Glia
|
July 19, 2001
Schwann cell myelination occurred without basal lamina formation in laminin alpha2 chain-null mutant (dy3K/dy3K) mice
M Nakagawa, Y Miyagoe-Suzuki, K Ikezoe, et al.
Journal of the Neurological Sciences
|
January 1, 1995
Fatal reducing body myopathy. Ultrastructural and immunohistochemical observations
B H Kiyomoto, N Murakami, Y Kobayashi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
March 23, 2006
Molecular pathomechanism of distal myopathy with rimmed vacuoles
I Nishino, May Christine V Malicdan, K Murayama, et al.
Human Pathology
|
January 1, 1990
Congenital nemaline myopathy with dilated cardiomyopathy: an autopsy study
H Ishibashi-Ueda, M Imakita, C Yutani, et al.
Cellular Immunology
|
November 1, 1986
Mitogenic heparin-binding lectin-like protein from cloned thymic myoid cells
I Kamo, S Furukawa, S Akazawa, et al.
Page
of 51
Search research articles
Search
Showing results (361-370 of 503) with videos related to
Sort By:
Page
of 51
Nature Genetics
|
October 4, 2000
Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes
K Inoue, K Nakada, A Ogura, et al.
Muscle & Nerve. Supplement
|
April 12, 2013
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses
K Arahata, T Ishihara, H Fukunaga, et al.
Neuroscience Letters
|
December 31, 1998
Up-regulation of glial cell line-derived neurotrophic factor (GDNF) expression in regenerating muscle fibers in neuromuscular diseases
H Suzuki, A Hase, B Y Kim, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
Presence of emerinopathy in cases of rigid spine syndrome
S Kubo, T Tsukahara, M Takemitsu, et al.
Neurology
|
July 11, 2001
Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy
Y K Hayashi, M Ogawa, K Tagawa, et al.
Glia
|
July 19, 2001
Schwann cell myelination occurred without basal lamina formation in laminin alpha2 chain-null mutant (dy3K/dy3K) mice
M Nakagawa, Y Miyagoe-Suzuki, K Ikezoe, et al.
Journal of the Neurological Sciences
|
January 1, 1995
Fatal reducing body myopathy. Ultrastructural and immunohistochemical observations
B H Kiyomoto, N Murakami, Y Kobayashi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
March 23, 2006
Molecular pathomechanism of distal myopathy with rimmed vacuoles
I Nishino, May Christine V Malicdan, K Murayama, et al.
Human Pathology
|
January 1, 1990
Congenital nemaline myopathy with dilated cardiomyopathy: an autopsy study
H Ishibashi-Ueda, M Imakita, C Yutani, et al.
Cellular Immunology
|
November 1, 1986
Mitogenic heparin-binding lectin-like protein from cloned thymic myoid cells
I Kamo, S Furukawa, S Akazawa, et al.
Page
of 51