Search research articles
Contact Us
Filters
Showing results (71-80 of 85) with videos related to
Page
of 9
Sort By:
Muscle & Nerve
|
January 14, 1998
A new congenital muscular dystrophy with mitochondrial structural abnormalities
I Nishino, O Kobayashi, Y Goto, et al.
Human Biology
|
April 1, 1994
Polymorphisms of complement component I and C1R subcomponent of C1 in nine aboriginal Taiwanese populations
K Umetsu, I Yuasa, T Suzuki, et al.
Journal of Human Genetics
|
April 27, 2001
Mitochondrial DNA polymorphisms in Yunnan nationalities in China
Y P Qian, Z T Chu, Q Dai, et al.
Tissue Antigens
|
March 1, 1981
The HLA antigens of two Negrito populations in the Philippines
S Horai, K Omoto, T Juji, et al.
Annals of Neurology
|
March 1, 1994
Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes
Y Kawakami, R Sakuta, K Hashimoto, et al.
Journal of the Neurological Sciences
|
September 1, 1989
Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS)
M Yoneda, M Tanaka, M Nishikimi, et al.
Biochemical and Biophysical Research Communications
|
August 15, 1988
Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy
T Ozawa, M Yoneda, M Tanaka, et al.
The American Journal of Physiology
|
September 1, 1994
Enzymatic and genetic adaptation of soleus muscle mitochondria to physical training in rats
T Murakami, Y Shimomura, N Fujitsuka, et al.
Nature Medicine
|
December 2, 1999
The presence of ancient human T-cell lymphotropic virus type I provirus DNA in an Andean mummy
H C Li, T Fujiyoshi, H Lou, et al.
American Journal of Human Genetics
|
September 1, 1996
mtDNA polymorphism in East Asian Populations, with special reference to the peopling of Japan
S Horai, K Murayama, K Hayasaka, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 85) with videos related to
Sort By:
Page
of 9
Muscle & Nerve
|
January 14, 1998
A new congenital muscular dystrophy with mitochondrial structural abnormalities
I Nishino, O Kobayashi, Y Goto, et al.
Human Biology
|
April 1, 1994
Polymorphisms of complement component I and C1R subcomponent of C1 in nine aboriginal Taiwanese populations
K Umetsu, I Yuasa, T Suzuki, et al.
Journal of Human Genetics
|
April 27, 2001
Mitochondrial DNA polymorphisms in Yunnan nationalities in China
Y P Qian, Z T Chu, Q Dai, et al.
Tissue Antigens
|
March 1, 1981
The HLA antigens of two Negrito populations in the Philippines
S Horai, K Omoto, T Juji, et al.
Annals of Neurology
|
March 1, 1994
Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes
Y Kawakami, R Sakuta, K Hashimoto, et al.
Journal of the Neurological Sciences
|
September 1, 1989
Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS)
M Yoneda, M Tanaka, M Nishikimi, et al.
Biochemical and Biophysical Research Communications
|
August 15, 1988
Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy
T Ozawa, M Yoneda, M Tanaka, et al.
The American Journal of Physiology
|
September 1, 1994
Enzymatic and genetic adaptation of soleus muscle mitochondria to physical training in rats
T Murakami, Y Shimomura, N Fujitsuka, et al.
Nature Medicine
|
December 2, 1999
The presence of ancient human T-cell lymphotropic virus type I provirus DNA in an Andean mummy
H C Li, T Fujiyoshi, H Lou, et al.
American Journal of Human Genetics
|
September 1, 1996
mtDNA polymorphism in East Asian Populations, with special reference to the peopling of Japan
S Horai, K Murayama, K Hayasaka, et al.
Page
of 9