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Biochemical and Biophysical Research Communications
|
October 18, 2000
FGF-20, a novel neurotrophic factor, preferentially expressed in the substantia nigra pars compacta of rat brain
S Ohmachi, Y Watanabe, T Mikami, et al.
Gerontology
|
January 1, 1992
Increased mitochondrial DNA deletions in the skeletal muscle of myotonic dystrophy
K Sahashi, M Tanaka, M Tashiro, et al.
Acta Neuropathologica
|
January 1, 1985
Immunohistochemical demonstration of carbonic anhydrase III and muscle-specific enolase in paraffin-embedded human skeletal muscle sections
T Ibi, H Haimoto, H Nagura, et al.
Journal of the Neurological Sciences
|
February 1, 1994
Multiplicity of abnormal dystrophin in Becker muscular dystrophy. A Becker muscular dystrophy gene frequently produced two smaller sizes of dystrophin
S Hori, S Ohtani, T Shimizu, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
February 1, 1991
[Myoglobinuria caused by multiple deletions of mitochondrial DNA]
M Tanaka, K Ohno, K Sahashi, et al.
Annals of Neurology
|
April 1, 1991
Mitochondrial DNA deletions in inherited recurrent myoglobinuria
K Ohno, M Tanaka, K Sahashi, et al.
Internal Medicine (Tokyo, Japan)
|
May 1, 1994
Immunostaining of dystrophin and utrophin in skeletal muscle of dystrophinopathies
K Sahashi, T Ibi, H Suoh, et al.
Journal of Animal Science
|
September 4, 2008
The use of link provider data to improve national genetic evaluation across weakly connected subpopulations
H Nakaoka, C Gaillard, K Fujinaka, et al.
Journal of the Neurological Sciences
|
November 1, 1990
Cytoplasmic body and mitochondrial DNA deletion
K Sahashi, K Ohno, M Tanaka, et al.
Biochimica Et Biophysica Acta
|
August 27, 1991
Direct DNA sequencing from colony: analysis of multiple deletions of mitochondrial genome
K Ohno, M Tanaka, H Ino, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 72) with videos related to
Sort By:
Page
of 8
Biochemical and Biophysical Research Communications
|
October 18, 2000
FGF-20, a novel neurotrophic factor, preferentially expressed in the substantia nigra pars compacta of rat brain
S Ohmachi, Y Watanabe, T Mikami, et al.
Gerontology
|
January 1, 1992
Increased mitochondrial DNA deletions in the skeletal muscle of myotonic dystrophy
K Sahashi, M Tanaka, M Tashiro, et al.
Acta Neuropathologica
|
January 1, 1985
Immunohistochemical demonstration of carbonic anhydrase III and muscle-specific enolase in paraffin-embedded human skeletal muscle sections
T Ibi, H Haimoto, H Nagura, et al.
Journal of the Neurological Sciences
|
February 1, 1994
Multiplicity of abnormal dystrophin in Becker muscular dystrophy. A Becker muscular dystrophy gene frequently produced two smaller sizes of dystrophin
S Hori, S Ohtani, T Shimizu, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
February 1, 1991
[Myoglobinuria caused by multiple deletions of mitochondrial DNA]
M Tanaka, K Ohno, K Sahashi, et al.
Annals of Neurology
|
April 1, 1991
Mitochondrial DNA deletions in inherited recurrent myoglobinuria
K Ohno, M Tanaka, K Sahashi, et al.
Internal Medicine (Tokyo, Japan)
|
May 1, 1994
Immunostaining of dystrophin and utrophin in skeletal muscle of dystrophinopathies
K Sahashi, T Ibi, H Suoh, et al.
Journal of Animal Science
|
September 4, 2008
The use of link provider data to improve national genetic evaluation across weakly connected subpopulations
H Nakaoka, C Gaillard, K Fujinaka, et al.
Journal of the Neurological Sciences
|
November 1, 1990
Cytoplasmic body and mitochondrial DNA deletion
K Sahashi, K Ohno, M Tanaka, et al.
Biochimica Et Biophysica Acta
|
August 27, 1991
Direct DNA sequencing from colony: analysis of multiple deletions of mitochondrial genome
K Ohno, M Tanaka, H Ino, et al.
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of 8