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I Nonaka

Showing results (291-300 of 503) with videos related to

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The Journal of Biological Chemistry|February 28, 1997
The interorganellar interaction between distinct human mitochondria with deletion mutant mtDNA from a patient with mitochondrial disease and with HeLa mtDNAD Takai, K Inoue, Y i Goto, et al.
Muscle & Nerve|December 1, 1996
The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)I Nishino, M Komatsu, S Kodama, et al.
Neuroscience Letters|September 27, 1996
Neural BC1 RNA in mouse skeletal muscle is a denervation-induced RNA whose expression is developmentally regulatedK Anzai, S Kobayashi, H Kotake, et al.
Pediatric Neurology|March 1, 1993
Fatal infantile mitochondrial encephalomyopathy with complex I and IV deficienciesT Nagai, Y Tuchiya, Y Taguchi, et al.
Bioscience, Biotechnology, and Biochemistry|May 1, 1997
In vitro and in vivo anti-platelet effects of enzymatic hydrolysates of collagen and collagen-related peptidesI Nonaka, S Katsuda, T Ohmori, et al.
Acta Neuropathologica|June 27, 2000
Expression of MyoD and myogenin in dystrophic mice, mdx and dy, during regenerationY Jin, N Murakami, Y Saito, et al.
No to Hattatsu = Brain and Development|January 6, 2001
[A patient of infantile polymyositis triggered by respiratory syncytium virus infection]T Nagasawa, H Sakuma, S Araki, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophyN Minami, K Ikezoe, H Kuroda, et al.
Journal of the Neurological Sciences|August 1, 1994
Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO)Y Hattori, Y Goto, R Sakuta, et al.
Brain & Development|September 1, 1993
Idiopathic lactic acidemia with developmental delay and type 1 muscle fiber atrophy: report of two patientsA Iso, N Murakami, H Yoneyama, et al.
Pageof 51

Showing results (291-300 of 503) with videos related to

Sort By:
Pageof 51
The Journal of Biological Chemistry|February 28, 1997
The interorganellar interaction between distinct human mitochondria with deletion mutant mtDNA from a patient with mitochondrial disease and with HeLa mtDNAD Takai, K Inoue, Y i Goto, et al.
Muscle & Nerve|December 1, 1996
The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)I Nishino, M Komatsu, S Kodama, et al.
Neuroscience Letters|September 27, 1996
Neural BC1 RNA in mouse skeletal muscle is a denervation-induced RNA whose expression is developmentally regulatedK Anzai, S Kobayashi, H Kotake, et al.
Pediatric Neurology|March 1, 1993
Fatal infantile mitochondrial encephalomyopathy with complex I and IV deficienciesT Nagai, Y Tuchiya, Y Taguchi, et al.
Bioscience, Biotechnology, and Biochemistry|May 1, 1997
In vitro and in vivo anti-platelet effects of enzymatic hydrolysates of collagen and collagen-related peptidesI Nonaka, S Katsuda, T Ohmori, et al.
Acta Neuropathologica|June 27, 2000
Expression of MyoD and myogenin in dystrophic mice, mdx and dy, during regenerationY Jin, N Murakami, Y Saito, et al.
No to Hattatsu = Brain and Development|January 6, 2001
[A patient of infantile polymyositis triggered by respiratory syncytium virus infection]T Nagasawa, H Sakuma, S Araki, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophyN Minami, K Ikezoe, H Kuroda, et al.
Journal of the Neurological Sciences|August 1, 1994
Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO)Y Hattori, Y Goto, R Sakuta, et al.
Brain & Development|September 1, 1993
Idiopathic lactic acidemia with developmental delay and type 1 muscle fiber atrophy: report of two patientsA Iso, N Murakami, H Yoneyama, et al.
Pageof 51