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Showing results (381-390 of 503) with videos related to

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Human Molecular Genetics|December 15, 2000
Caveolin-3 deficiency causes muscle degeneration in miceY Hagiwara, T Sasaoka, K Araishi, 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 dystrophinS Hori, S Ohtani, T Shimizu, et al.
Muscle & Nerve|July 1, 1997
Marinesco-Sjogren syndrome: can the diagnosis be made prior to cataract formation?T Shimizu, T Matsuishi, Y Yamashita, et al.
Neuropediatrics|February 1, 1988
Atypical form of Menkes kinky hair disease with mitochondrial NADH-CoQ reductase deficiencyM Inagaki, K Hashimoto, K Yoshino, et al.
Clinical Endocrinology|November 1, 1996
Hypoparathyroidism and insulin-dependent diabetes mellitus in a patient with Kearns-Sayre syndrome harbouring a mitochondrial DNA deletionH Isotani, Y Fukumoto, H Kawamura, et al.
Biochemical and Biophysical Research Communications|July 15, 1994
Decreased myotonin-protein kinase in the skeletal and cardiac muscles in myotonic dystrophyR Koga, Y Nakao, Y Kurano, et al.
American Journal of Human Genetics|January 1, 1994
Three new mutations in patients with myophosphorylase deficiency (McArdle disease)S Tsujino, S Shanske, I Nonaka, et al.
Acta Neuropathologica|January 1, 1996
Basement membrane abnormality in merosin-negative congenital muscular dystrophyS Osari, O Kobayashi, Y Yamashita, et al.
Journal of Dairy Science|October 21, 2009
Difference in the nature of tannins on in vitro ruminal methane and volatile fatty acid production and on methanogenic archaea and protozoal populationsR Bhatta, Y Uyeno, K Tajima, et al.
Annals of Neurology|April 13, 2000
A novel congenital myopathy with apoptotic changesK Ikezoe, C Yan, T Momoi, et al.
Pageof 51

Showing results (381-390 of 503) with videos related to

Sort By:
Pageof 51
Human Molecular Genetics|December 15, 2000
Caveolin-3 deficiency causes muscle degeneration in miceY Hagiwara, T Sasaoka, K Araishi, 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 dystrophinS Hori, S Ohtani, T Shimizu, et al.
Muscle & Nerve|July 1, 1997
Marinesco-Sjogren syndrome: can the diagnosis be made prior to cataract formation?T Shimizu, T Matsuishi, Y Yamashita, et al.
Neuropediatrics|February 1, 1988
Atypical form of Menkes kinky hair disease with mitochondrial NADH-CoQ reductase deficiencyM Inagaki, K Hashimoto, K Yoshino, et al.
Clinical Endocrinology|November 1, 1996
Hypoparathyroidism and insulin-dependent diabetes mellitus in a patient with Kearns-Sayre syndrome harbouring a mitochondrial DNA deletionH Isotani, Y Fukumoto, H Kawamura, et al.
Biochemical and Biophysical Research Communications|July 15, 1994
Decreased myotonin-protein kinase in the skeletal and cardiac muscles in myotonic dystrophyR Koga, Y Nakao, Y Kurano, et al.
American Journal of Human Genetics|January 1, 1994
Three new mutations in patients with myophosphorylase deficiency (McArdle disease)S Tsujino, S Shanske, I Nonaka, et al.
Acta Neuropathologica|January 1, 1996
Basement membrane abnormality in merosin-negative congenital muscular dystrophyS Osari, O Kobayashi, Y Yamashita, et al.
Journal of Dairy Science|October 21, 2009
Difference in the nature of tannins on in vitro ruminal methane and volatile fatty acid production and on methanogenic archaea and protozoal populationsR Bhatta, Y Uyeno, K Tajima, et al.
Annals of Neurology|April 13, 2000
A novel congenital myopathy with apoptotic changesK Ikezoe, C Yan, T Momoi, et al.
Pageof 51