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S Horai

Showing results (51-60 of 85) with videos related to

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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.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|September 30, 1991
Phylogenetic affiliation of ancient and contemporary humans inferred from mitochondrial DNAS Horai, R Kondo, K Murayama, et al.
The Journal of Pediatrics|June 1, 1990
Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndromeY Goto, N Itami, N Kajii, et al.
Journal of Child Neurology|April 1, 1993
A T-to-G mutation at nucleotide pair 8993 in mitochondrial DNA in a patient with Leigh's syndromeH Yoshinaga, T Ogino, S Ohtahara, et al.
Tissue Antigens|May 1, 1982
The outcome of cell mediated lympholysis is influenced by the antibiotics in the culture mediumS Horai, F H Claas, J J vd Poel, et al.
Biochimica Et Biophysica Acta|November 2, 1989
Specific amplification of deleted mitochondrial DNA from a myopathic patient and analysis of deleted region with S1 nucleaseT Tanaka-Yamamoto, M Tanaka, K Ohno, et al.
Molecular Biology and Evolution|January 1, 1993
Peopling of the Americas, founded by four major lineages of mitochondrial DNAS Horai, R Kondo, Y Nakagawa-Hattori, et al.
Neurology|March 1, 1992
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutationY Goto, S Horai, T Matsuoka, et al.
Annals of Neurology|October 1, 1992
Mitochondrial DNA mutation and Leigh's syndromeR Sakuta, Y Goto, S Horai, et al.
Lancet (London, England)|May 13, 1989
Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathyM Yoneda, S Tsuji, T Yamauchi, et al.
Pageof 9

Showing results (51-60 of 85) with videos related to

Sort By:
Pageof 9
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.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|September 30, 1991
Phylogenetic affiliation of ancient and contemporary humans inferred from mitochondrial DNAS Horai, R Kondo, K Murayama, et al.
The Journal of Pediatrics|June 1, 1990
Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndromeY Goto, N Itami, N Kajii, et al.
Journal of Child Neurology|April 1, 1993
A T-to-G mutation at nucleotide pair 8993 in mitochondrial DNA in a patient with Leigh's syndromeH Yoshinaga, T Ogino, S Ohtahara, et al.
Tissue Antigens|May 1, 1982
The outcome of cell mediated lympholysis is influenced by the antibiotics in the culture mediumS Horai, F H Claas, J J vd Poel, et al.
Biochimica Et Biophysica Acta|November 2, 1989
Specific amplification of deleted mitochondrial DNA from a myopathic patient and analysis of deleted region with S1 nucleaseT Tanaka-Yamamoto, M Tanaka, K Ohno, et al.
Molecular Biology and Evolution|January 1, 1993
Peopling of the Americas, founded by four major lineages of mitochondrial DNAS Horai, R Kondo, Y Nakagawa-Hattori, et al.
Neurology|March 1, 1992
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutationY Goto, S Horai, T Matsuoka, et al.
Annals of Neurology|October 1, 1992
Mitochondrial DNA mutation and Leigh's syndromeR Sakuta, Y Goto, S Horai, et al.
Lancet (London, England)|May 13, 1989
Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathyM Yoneda, S Tsuji, T Yamauchi, et al.
Pageof 9