S. Horai

发表

Intraspecific nucleotide sequence differences in the major noncoding region of human mitochondrial DNA.

S. Horai, K. Hayasaka, 1990, American journal of human genetics.

Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs.

N. Takahata, S. Horai, K. Hayasaka, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Molecular phylogeny and evolution of prosimians based on complete sequences of mitochondrial DNAs.

M. Hasegawa, S. Horai, A. Matsui, 2009, Gene.

The presence of ancient human T-cell lymphotropic virus type I provirus DNA in an Andean mummy

S. Horai, K. Tajima, Hong-Chuan Li, 1999, Nature Medicine.

Molecular phylogeny and evolution of primate mitochondrial DNA.

T Gojobori, T. Gojobori, S. Horai, 1988, Molecular biology and evolution.

Mitochondrial DNA polymorphisms in nine aboriginal groups of Taiwan: implications for the population history of aboriginal Taiwanese

Naruya Saitou, Takafumi Ishida, N. Saitou, 2003, Human Genetics.

Mitochondrial DNA mutations at nucleotide positions 3243 and 3271 in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: A comparative study

R. Sakuta, I. Nonaka, S. Horai, 1993, Journal of the Neurological Sciences.

Chronic progressive external ophthalmoplegia: A correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies

Ikuya Nonaka, I. Nonaka, S. Horai, 1990, Journal of the Neurological Sciences.

Differential recognition of the serologically defined HLA-A2 antigen by allogeneic cytotoxic T Cells

S. Horai, E. Goulmy, J. Poel, 1982, Immunogenetics.

A Caucasian family with the 3271 mutation in mitochondrial DNA.

M. Passos-Bueno, M. Zatz, Y. Goto, 1994, Biochemical medicine and metabolic biology.

Mitochondrial Myopathies: Morphological Approach to Molecular Abnormalities

S. Horai, T. Ozawa, Shinji Nakamura, 1990 .

DNA Amplification from Ancient Human Skeletal Remains and Their Sequence Analysis

S. Horai, K. Hayasaka, N. Nakai, 1989 .

Increased level of mitochondrial gene expression in polyps of familial polyposis coli patients.

S. Horai, Y. Yuasa, A. Yamamoto, 1989, Biochemical and biophysical research communications.

The geographic distribution of human Y chromosome variation.

R J Mitchell, R. J. Mitchell, M. Hammer, 1997, Genetics.

Y chromosomal DNA variation and the peopling of Japan.

M. Hammer, S. Horai, Michael F. Hammer, 1995, American journal of human genetics.

mtDNA polymorphism in East Asian Populations, with special reference to the peopling of Japan.

S. Horai, K. Hayasaka, K. Park, 1996, American journal of human genetics.

Genetic background of people in the Dominican Republic with or without obese type 2 diabetes revealed by mitochondrial DNA polymorphism

S. Horai, A. Tajima, K. Hamaguchi, 2004, Journal of Human Genetics.

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS)

Y. Goto, I. Nonaka, S. Horai, 1992, Neurology.

A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

I. Nonaka, S. Horai, Yu-ichi Goto, 1990, Nature.

Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications

I. Nonaka, S. Horai, M. Makino, 2000, Journal of Human Genetics.

Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome.

S. Horai, N. Itami, N. Kajii, 1990, The Journal of pediatrics.

Molecular phylogeny of macaques: implications of nucleotide sequences from an 896-base pair region of mitochondrial DNA.

S. Horai, K. Hayasaka, K. Fujii, 1996, Molecular biology and evolution.

Mitochondrial DNA polymorphisms in Yunnan nationalities in China

Y. Qian, S. Horai, Q. Dai, 2001, Journal of Human Genetics.

Mitochondrial DNA polymorphism in Japanese

S. Horai, E. Matsunaga, 1986, Human Genetics.

Mitochondrial DNA polymorphism in Japanese

T. Gojobori, S. Horai, E. Matsunaga, 2004, Human Genetics.

Distribution of the 9-bp deletion in COII/tRNA^ intergenic region of mitochondrial DNA is relatively homogeneous in east Asian populations

S. Horai, C. H. Lee, S. Hong, 1998 .

Peopling of the Americas, founded by four major lineages of mitochondrial DNA.

S. Horai, R. Kondo, K. Tajima, 1994, Molecular biology and evolution.

Phylogenetic affiliation of ancient and contemporary humans inferred from mitochondrial DNA.

S. Horai, R. Kondo, N. Nakai, 1991, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

A Genetic Trail of Human Mitochondrial DNA

S. Horai, 1991 .

Phylogenetic relationships among Japanese, rhesus, Formosan, and crab-eating monkeys, inferred from restriction-enzyme analysis of mitochondrial DNAs.

T. Gojobori, S. Horai, K. Hayasaka, 1988, Molecular biology and evolution.

Evolutionary Implications of Mitochondrial DNA Polymorphism in Human Populations

T. Gojobori, S. Horai, E. Matsunaga, 1987 .

Mitochondrial DNA polymorphism in Japanese monkeys, Macaca fuscata

S. Horai, K. Hayasaka, E. Matsunaga, 1986 .

I. Analysis with restriction enzymes of six base pair recognition

T. Gojobori, S. Horai, E. Matsunaga, 1984 .

Evolution of hominoid mitochondrial DNA with special reference to the silent substitution rate over the genome

N. Takahata, S. Horai, R. Kondo, 1993, Journal of Molecular Evolution.

HLA-A, HLA-B, and HLA-DRB1 alleles and haplotypes in Naxi and Han populations in southwestern China (Yunnan province).

K. Tokunaga, S. Horai, J. Ohashi, 2006, Tissue antigens.

Molecular phylogeny of gibbons inferred from mitochondrial DNA sequences: Preliminary report

S. Horai, K. Hayasaka, O. Takenaka, 1995, Journal of Molecular Evolution.

Determination of a complete lemur mitochondrial genome from feces

M. Hasegawa, S. Horai, A. Matsui, 2007 .

Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS)

Hiroshi Suzuki, T. Miyatake, S. Horai, 1989, Journal of the Neurological Sciences.

Mitochondrial DNA evolution in primates: Transition rate has been extremely low in the lemur

H. Kishino, M. Hasegawa, S. Horai, 1990, Journal of Molecular Evolution.

Man's place in hominoidea revealed by mitochondrial DNA genealogy

N. Takahata, S. Horai, K. Hayasaka, 1992, Journal of Molecular Evolution.

Molecular phylogeny of gibbons inferred from mitochondrial DNA sequences: Preliminary report

S. Horai, K. Hayasaka, O. Takenaka, 2004, Journal of Molecular Evolution.

Myoclonus epilepsy associated with ragged‐red fibers: A G‐to‐A mutation at nucleotide pair 8363 in mitochondrial tRNALys in two families

I. Nonaka, I. Nishino, S. Horai, 1997, Muscle & nerve.

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

Y. Goto, I. Nonaka, S. Horai, 1991, Biochimica et biophysica acta.

A common mitochondrial DNA mutation in the t-RNA(Lys) of patients with myoclonus epilepsy associated with ragged-red fibers.

S. Tsuji, S. Horai, M. Yoneda, 1990, Biochemistry international.

Time of the deepest root for polymorphism in human mitochondrial DNA

M. Hasegawa, S. Horai, 2005, Journal of Molecular Evolution.

A new congenital muscular dystrophy with mitochondrial structural abnormalities

I. Nonaka, I. Nishino, S. Horai, 1998, Muscle & nerve.

Distribution of HLA alleles and haplotypes in Jinuo and Wa populations in Southwest China.

M. Muramatsu, K. Tokunaga, S. Horai, 2008, Human immunology.

Mitochondrial DNA polymorphism in Japanese. II. Analysis with restriction enzymes of four or five base pair recognition.

S. Horai, E. Matsunaga, 1986, Human genetics.

Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia

K. Tokunaga, S. Horai, M. Matsuo, 2001, Human Genetics.

Haplotype analysis of the linkage group HLA-A: HLA-B: Bf in Japanese

S. Horai, T. Juji, H. Nakajima, 1979, Human Genetics.

Polymorphism of the HLA-DRB1 locus in Colombian, Ecuadorian, and Chilean Amerinds.

D. Watkins, J. Klein, S. Horai, 1997, Human immunology.

The distribution of the phosphoglucomutase-I (PGM1) subtypes in Japanese

S. Horai, K. Omoto, Yukiko Maneyama, 1978, Japanese Journal of Human Genetics.

Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes

M. Hammer, M. Stoneking, S. Horai, 2006, Journal of Human Genetics.

Genetic polymorphism of human serum factor B (Bf) in Japanese.

S. Horai, 1976, Jinrui idengaku zasshi. The Japanese journal of human genetics.

Haplotype analysis of the linkage group HLA-A:HLA-B:C4 in Japanese: Evidence for the C4 locus being between the HLA-A and HLA-B loci

K. Tokunaga, S. Horai, T. Juji, 1980, Japanese Journal of Human Genetics.

Genetic polymorphism of the fourth component of human complement in Japanese

K. Tokunaga, S. Horai, T. Juji, 1979, Japanese Journal of Human Genetics.

Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages

K. Tokunaga, S. Horai, M. Matsuo, 2004, Journal of Human Genetics.

A T-to-G Mutation at Nucleotide Pair 8993 in Mitochondrial DNA in a Patient With Leigh's Syndrome

R. Sakuta, I. Nonaka, H. Yoshinaga, 1993, Journal of child neurology.

Population Genetic Studies on Nine Aboriginal Ethnic Groups of Taiwan II. Serum Protein Systems

N. Saitou, S. Horai, T. Ishida, 2001 .

Orosomucoid phenotyping with monoclonal antibodies:polymorphic occurrence of ORM1*Q0 in aboriginal Taiwanese populations.

N. Saitou, S. Horai, T. Ishida, 1995, Human heredity.

Genetic Polymorphism of ADA in Taiwan Aboriginal Populations: New ADA Variants Detected by Isoelectric Focusing Method

N. Saitou, S. Horai, T. Ishida, 1995 .

Polymorphisms of complement component I and C1R subcomponent of C1 in nine aboriginal Taiwanese populations.

N. Saitou, S. Horai, T. Ishida, 1994, Human biology.

Seroepidemiological survey of human T-lymphotropic retrovirus among indigenous populations in Taiwan.

N. Saitou, S. Horai, T. Ishida, 1993, International journal of epidemiology.

Mitochondrial DNA polymorphisms in Thailand

S. Horai, G. Fucharoen, S. Fucharoen, 2001, Journal of Human Genetics.

Insertion near the mitochondrial tyrosine tRNA gene in patients with mitochondrial diseases

I. Nonaka, S. Horai, Yu-ichi Goto, 1994 .

Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO)

R. Sakuta, I. Nonaka, S. Horai, 1994, Journal of the Neurological Sciences.

Heteroplasmy and polymorphism in the major noncoding region of mitochondrial DNA in Japanese monkeys: association with tandemly repeated sequences.

S. Horai, K. Hayasaka, T. Ishida, 1991, Molecular biology and evolution.

A novel mutation in the mitochondrial tRNA(Thr) gene associated with a mitochondrial encephalomyopathy.

Y. Goto, I. Nonaka, I. Nishino, 1996, Biochemical and biophysical research communications.

Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndrome

I. Nonaka, S. Horai, M. Makino, 1998, Neuromuscular Disorders.

Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation.

S. Horai, S. Usami, S. Abe, 2005, Auris, nasus, larynx.

Enzymatic and genetic adaptation of soleus muscle mitochondria to physical training in rats.

M. Sokabe, S. Horai, N. Nakai, 1994, The American journal of physiology.

The HLA antigens of two Negrito populations in the Philippines.

S. Horai, H. Mitsui, T. Juji, 2008, Tissue antigens.

Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy.

K. Ohno, I. Nonaka, S. Horai, 1988, Biochemical and biophysical research communications.

Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation

W. Kimberling, S. Horai, S. Usami, 1998, European Journal of Human Genetics.

Distinct clustering of mitochondrial DNA types among Japanese, Caucasians and Negroes

T. Gojobori, S. Horai, E. Matsunaga, 1986 .

Is Parkinson's disease a mitochondrial disorder?

S. Horai, H. Yoshino, Y. Mizuno, 1992, Journal of the Neurological Sciences.

Severe lactic acidosis and neonatal death in Pearson syndrome

Y. Goto, I. Nishino, S. Horai, 1997, Journal of Inherited Metabolic Disease.

MITOCHONDRIAL DNA MUTATION IN FAMILY WITH LEBER'S HEREDITARY OPTIC NEUROPATHY

S. Tsuji, T. Miyatake, S. Horai, 1989, The Lancet.

The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

I. Nonaka, I. Nishino, S. Horai, 1996, Muscle & nerve.

A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

Y. Goto, I. Nonaka, S. Horai, 1994, Biochemical and biophysical research communications.

A novel point mutation in the mitochondrial tRNALeu(UUR) gene in a family with mitochondrial myopathy

I. Nonaka, S. Horai, J. Tohyama, 1992, Annals of neurology.

Mitochondrial DNA mutation and Leigh's syndrome

R. Sakuta, I. Nonaka, H. Yoshinaga, 1992, Annals of neurology.

Specific amplification of deleted mitochondrial DNA from a myopathic patient and analysis of deleted region with S1 nuclease.

K. Ohno, S. Horai, T. Ozawa, 1989, Biochimica et biophysica acta.

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

R. Sakuta, Y. Goto, I. Nonaka, 1994, The New England journal of medicine.

Detection of DNA fragments encompassing the deletion junction of mitochondrial genome.

Y. Goto, I. Nonaka, I. Nishino, 1996, Biochemical and Biophysical Research Communications - BBRC.

Evolution and the origins of man: clues from complete sequences of hominoid mitochondrial DNA.

S. Horai, 1995, The Southeast Asian journal of tropical medicine and public health.

[Peopling of the Americas, founded by four major lineages of mitochondrial DNA].

S. Horai, 1994, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

An A-to-G transition at nucleotide pair 11084 in the ND4 gene may be an mtDNA polymorphism.

R. Sakuta, Y. Goto, I. Nonaka, 1993, American journal of human genetics.

In situ hybridization of muscle mitochondrial mRNA in mitochondrial myopathies

S. Horai, H. Ujike, Y. Fukuda, 2004, Acta Neuropathologica.

Mitochondrial myopathy with progressive decrease in mitochondrial tRNALeu(UUR) mutant genomes

R. Sakuta, I. Nonaka, S. Horai, 1994, Annals of neurology.