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S Horai

Showing results (61-70 of 85) with videos related to

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Biochemical and Biophysical Research Communications|August 5, 1996
A novel mutation in the mitochondrial tRNA(Thr) gene associated with a mitochondrial encephalomyopathyI Nishino, A Seki, Y Maegaki, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
Severe lactic acidosis and neonatal death in Pearson syndromeK Muraki, Y Goto, I Nishino, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Differently deleted mitochondrial genomes in maternally inherited chronic progressive external ophthalmoplegiaM Tanaka, M Yoneda, K Ohno, et al.
Biological & Pharmaceutical Bulletin|September 18, 2001
Transdermal drug delivery by electroporation applied on the stratum corneum of rat using stamp-type electrode and frog-type electrode in vitroS Fukushima, S Kishimoto, S Horai, et al.
Journal of Molecular Evolution|July 1, 1993
Man's place in Hominoidea revealed by mitochondrial DNA genealogyS Horai, Y Satta, K Hayasaka, et al.
Journal of Molecular Evolution|July 1, 1992
Man's place in Hominoidea revealed by mitochondrial DNA genealogyS Horai, Y Satta, K Hayasaka, et al.
Human Immunology|April 15, 1997
Polymorphism of the HLA-DRB1 locus in Colombian, Ecuadorian, and Chilean AmerindsN Blagitko, C O'hUigin, F Figueroa, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|May 2, 2001
[Genetic relationship among four Yunnan populations revealed by sequence of mtDNA D-loop]Y P Qian, J Y Chu, Z T Chu, et al.
Acta Neuropathologica|January 1, 1990
In situ hybridization of muscle mitochondrial mRNA in mitochondrial myopathiesS Nakamura, T Sato, H Hirawake, et al.
Human Heredity|July 1, 1995
Orosomucoid phenotyping with monoclonal antibodies:polymorphic occurrence of ORM1*Q0 in aboriginal Taiwanese populationsK Umetsu, I Yuasa, A Harada, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
Biochemical and Biophysical Research Communications|August 5, 1996
A novel mutation in the mitochondrial tRNA(Thr) gene associated with a mitochondrial encephalomyopathyI Nishino, A Seki, Y Maegaki, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
Severe lactic acidosis and neonatal death in Pearson syndromeK Muraki, Y Goto, I Nishino, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Differently deleted mitochondrial genomes in maternally inherited chronic progressive external ophthalmoplegiaM Tanaka, M Yoneda, K Ohno, et al.
Biological & Pharmaceutical Bulletin|September 18, 2001
Transdermal drug delivery by electroporation applied on the stratum corneum of rat using stamp-type electrode and frog-type electrode in vitroS Fukushima, S Kishimoto, S Horai, et al.
Journal of Molecular Evolution|July 1, 1993
Man's place in Hominoidea revealed by mitochondrial DNA genealogyS Horai, Y Satta, K Hayasaka, et al.
Journal of Molecular Evolution|July 1, 1992
Man's place in Hominoidea revealed by mitochondrial DNA genealogyS Horai, Y Satta, K Hayasaka, et al.
Human Immunology|April 15, 1997
Polymorphism of the HLA-DRB1 locus in Colombian, Ecuadorian, and Chilean AmerindsN Blagitko, C O'hUigin, F Figueroa, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|May 2, 2001
[Genetic relationship among four Yunnan populations revealed by sequence of mtDNA D-loop]Y P Qian, J Y Chu, Z T Chu, et al.
Acta Neuropathologica|January 1, 1990
In situ hybridization of muscle mitochondrial mRNA in mitochondrial myopathiesS Nakamura, T Sato, H Hirawake, et al.
Human Heredity|July 1, 1995
Orosomucoid phenotyping with monoclonal antibodies:polymorphic occurrence of ORM1*Q0 in aboriginal Taiwanese populationsK Umetsu, I Yuasa, A Harada, et al.
Pageof 9