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Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1989
Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses
K Arahata, E P Hoffman, L M Kunkel, et al.
No to Hattatsu = Brain and Development
|
July 1, 1997
[Cousins with X-linked recessive myotubular myopathy]
Y Mori, S Kaneko, T Nakayama, et al.
Neurology
|
October 12, 2005
A new congenital form of X-linked autophagic vacuolar myopathy
C Yan, M Tanaka, K Sugie, et al.
American Journal of Human Genetics
|
August 1, 1993
Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin
K Matsumura, I Nonaka, F M Tomé, et al.
Uchu Seibutsu Kagaku
|
May 9, 2002
[Gene expression in skeletal muscle of spaceflight rat]
T Nikawa, M Ikemoto, M Kano, et al.
Nature Genetics
|
November 1, 1993
Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33
T Toda, M Segawa, Y Nomura, et al.
Innate Immunity
|
October 30, 2016
C4b binding protein negatively regulates TLR1/2 response
Naoko Morita, Ikuko Yamai, Koichiro Takahashi, et al.
Annals of Neurology
|
December 16, 1998
Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy
S Kimura, S Sugino, Y Ohtani, et al.
Neurology
|
June 1, 2007
Congenital neuromuscular disease with uniform type 1 fiber and RYR1 mutation
I Sato, S Wu, M C A Ibarra, et al.
Advances in Biophysics
|
January 1, 1996
Structure and physiological functions of ubiquitous and tissue-specific calpain species. Muscle-specific calpain, p94, interacts with connectin/titin
H Sorimachi, S Kimura, K Kinbara, et al.
Page
of 51
Search research articles
Search
Showing results (471-480 of 503) with videos related to
Sort By:
Page
of 51
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1989
Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses
K Arahata, E P Hoffman, L M Kunkel, et al.
No to Hattatsu = Brain and Development
|
July 1, 1997
[Cousins with X-linked recessive myotubular myopathy]
Y Mori, S Kaneko, T Nakayama, et al.
Neurology
|
October 12, 2005
A new congenital form of X-linked autophagic vacuolar myopathy
C Yan, M Tanaka, K Sugie, et al.
American Journal of Human Genetics
|
August 1, 1993
Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin
K Matsumura, I Nonaka, F M Tomé, et al.
Uchu Seibutsu Kagaku
|
May 9, 2002
[Gene expression in skeletal muscle of spaceflight rat]
T Nikawa, M Ikemoto, M Kano, et al.
Nature Genetics
|
November 1, 1993
Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33
T Toda, M Segawa, Y Nomura, et al.
Innate Immunity
|
October 30, 2016
C4b binding protein negatively regulates TLR1/2 response
Naoko Morita, Ikuko Yamai, Koichiro Takahashi, et al.
Annals of Neurology
|
December 16, 1998
Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy
S Kimura, S Sugino, Y Ohtani, et al.
Neurology
|
June 1, 2007
Congenital neuromuscular disease with uniform type 1 fiber and RYR1 mutation
I Sato, S Wu, M C A Ibarra, et al.
Advances in Biophysics
|
January 1, 1996
Structure and physiological functions of ubiquitous and tissue-specific calpain species. Muscle-specific calpain, p94, interacts with connectin/titin
H Sorimachi, S Kimura, K Kinbara, et al.
Page
of 51