T. Shinka

发表

Climatic influence on the reproductive characteristics of Japanese males

A. Ewis, T. Iwamoto, Y. Nakahori, 2012, Journal of Human Genetics.

Association of estrogen receptor alpha gene polymorphisms and lifestyle factors with calcaneal quantitative ultrasound and osteoporosis in postmenopausal Vietnamese women.

Y. Nakahori, V. Hien, Shigeru Yamamoto, 2006 .

Two Y-chromosome-specific polymorphisms 12f2 and DFFRY in the Japanese population and their relations to other Y-polymorphisms.

A. Ewis, Y. Nakahori, T. Shinka, 2002, The journal of medical investigation : JMI.

A rapid and simple method for sex identification by heteroduplex analysis, using denaturing high-performance liquid chromatography (DHPLC)

T. Naroda, Y. Nakahori, T. Tamura, 2001, Journal of Human Genetics.

Direct Correlation Between Ischemic Injury and Extracellular Glycine Concentration in Mice With Genetically Altered Activities of the Glycine Cleavage Multienzyme System

T. Sugawara, M. Oda, H. Kinouchi, 2007, Stroke.

Spermatogenic ability is different among males in different Y chromosome lineage

Y. Kuroki, K. Tokunaga, A. Ewis, 1999, Journal of Human Genetics.

Y Chromosome gr/gr Subdeletion Is Associated with Lower Semen Quality in Young Men from the General Japanese Population but Not in Fertile Japanese Men1

T. Iwamoto, Y. Nakahori, M. Namiki, 2014, Biology of reproduction.

Y Chromosome gr/gr Subdeletion Is Associated with Lower Semen Quality in Young Men from the General Japanese Population but Not in Fertile Japanese Men 1 Running Title: GR/GR SUBDELETION AND FERTILITY

Y. Nakahori, M. Namiki, A. Yamauchi, 2014 .

Proteasome Subunits mRNA Expressions Correlate With Male BMI: Implications for a Role in Obesity

A. Ewis, Y. Nakahori, Youichi Sato, 2009, Obesity.

Altered expression pattern of heat shock transcription factor, Y chromosome (HSFY) may be related to altered differentiation of spermatogenic cells in testes with deteriorated spermatogenesis.

Yoko Sato, T. Iwamoto, Y. Nakahori, 2006, Fertility and sterility.

Genetic variations on the Y chromosome in the Japanese population and implications for modern human Y chromosome lineage

Y. Kuroki, K. Tokunaga, T. Toda, 1999, Journal of Human Genetics.

Overview of genetic variation in the Y chromosome of modern Japanese males

A. Ewis, T. Iwamoto, Y. Nakahori, 2014 .

Y Chromosome Haplogroup D2* Lineage Is Associated with Azoospermia in Japanese Males1

T. Iwamoto, Y. Nakahori, A. Yamauchi, 2013, Biology of reproduction.

Y chromosome compound haplotypes with the microsatellite markers DXYS265, DXYS266, and DXYS241

Y. Kuroki, K. Tokunaga, A. Ewis, 2001, Journal of Human Genetics.

Overexpression of SOX15 inhibits proliferation of NT2/D1 cells derived from a testicular embryonal cell carcinoma.

H. Aburatani, Gang Chen, K. Kinoshita, 2007, Molecules and cells.

Mutation and polymorphic marker analyses of 65K- and 67K-glutamate decarboxylase genes in two families with pyridoxine-dependent epilepsy

Kazutoshi Takahashi, Y. Matsubara, K. Narisawa, 1998, Journal of Human Genetics.

Survey of the two polymorphisms in DAZL, an autosomal candidate for the azoospermic factor, in Japanese infertile men and implications for male infertility.

Gang Chen, T. Iwamoto, Y. Nakahori, 2005, Molecular human reproduction.

A rapid and simple system of detecting deletions on the Y chromosome related with male infertility using multiplex PCR.

Y. Baba, T. Iwamoto, Y. Nakahori, 2006, The journal of medical investigation : JMI.

The azoospermic factor on the Y chromosome

Y. Nakahori, T. Shinka, TOSHIKATSU SHINKA, 1996, Acta paediatrica Japonica : Overseas edition.

Dinucleotide repeat polymorphism in 65k-glutamate decarboxylase gene

Y. Matsubara, K. Narisawa, Y. Aoki, 1997, Japanese Journal of Human Genetics.

Yfm1, a multicopy marker specific for the Y chromosome and beneficial for forensic, population, genetic, and spermatogenesis-related studies

Y. Kuroki, A. Ewis, Y. Nakahori, 2002, Journal of Human Genetics.

Microdeletions of a Y-specific marker, Yfm1, and implications for a role in spermatogenesis

A. Ewis, Y. Nakahori, T. Shinka, 2002, Journal of Human Genetics.

Rapid multiplexing and simultaneous detection of human spermatogenetic failure with a 12 lane microchip electrophoresis system.

N. Kaji, M. Tokeshi, Y. Baba, 2006, Biological & pharmaceutical bulletin.

Expression analysis of a mouse orthologue of HSFY, a candidate for the azoospermic factor on the human Y chromosome.

H. Kurahashi, S. Ito, K. Toida, 2006, The journal of medical investigation : JMI.

Roles of estrogen receptor alpha (ER alpha) in the regulation of the human Müllerian inhibitory substance (MIS) promoter.

Gang Chen, K. Kinoshita, T. Iwamoto, 2003, The journal of medical investigation : JMI.

Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly

Naoto Endo, Peter Heutink, Minoru Shibata, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Molecular analysis of TBL1Y, a Y-linked homologue of TBL1X related with X-linked late-onset sensorineural deafness

Gang Chen, K. Kinoshita, Y. Unemi, 2005, Journal of Human Genetics.

The male-determining gene SRY is a hybrid of DGCR8 and SOX3, and is regulated by the transcription factor CP2

A. Ewis, Y. Nakahori, Youichi Sato, 2010, Molecular and Cellular Biochemistry.

Structure and expression of the glycine cleavage system in rat central nervous system.

K. Hisanaga, J. Satoh, Kohji Sato, 2001, Brain research. Molecular brain research.

Chromosomal localization, structure, single-nucleotide polymorphisms, and expression of the human H-protein gene of the glycine cleavage system (GCSH), a candidate gene for nonketotic hyperglycinemia

Y. Matsubara, K. Narisawa, Y. Aoki, 2001, Journal of Human Genetics.

Assignment1 of Gldc encoding glycine decarboxylase to mouse chromosome 19C by in situ hybridization and a CA repeat polymorphism in the Gldc gene

Y. Matsubara, K. Narisawa, S. Kure, 1998, Cytogenetic and Genome Research.

A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemia

Y. Matsubara, K. Narisawa, K. Tada, 1998, Journal of Human Genetics.

A missense mutation (His42Arg) in the T-protein gene from a large Israeli-Arab kindred with nonketotic hyperglycinemia

Yoichi Matsubara, Hanna Mandel, H. Mandel, 1998, Human Genetics.

Model Mice for Mild-Form Glycine Encephalopathy: Behavioral and Biochemical Characterizations and Efficacy of Antagonists for the Glycine Binding Site of N-Methyl D-Aspartate Receptor

T. Sugawara, M. Oda, Y. Matsubara, 2008, Pediatric Research.

A/G heterozygote of the A-3826G polymorphism in the UCP-1 gene has higher BMI than A/A and G/G homozygote in young Japanese males.

Yoichi Sato, Y. Nakahori, M. Umeno, 2006, The journal of medical investigation : JMI.

Proteomics and transcriptome approaches to investigate the mechanism of human sex determination

H. Aburatani, A. Ewis, Gang Chen, 2009, Cell biology international.

Y-chromosomal DNA haplogroups and their implications for the dual origins of the Koreans

M. Hammer, C. Tyler-Smith, H. Jin, 2003, Human Genetics.

Y chromosomal STRs haplotypes in two populations from Bolivia.

M. Hurles, H. Kashiwazaki, A. Ewis, 2007, Legal medicine.

Candidate genes for male factor infertility--validation.

H. Kurahashi, T. Toda, T. Iwamoto, 2006, Fertility and sterility.

Occupational cancer genetics: infrequent ras oncogenes point mutations in lung cancer samples from chromate workers.

K. Kondo, Y. Monden, A. Ewis, 2001, American journal of industrial medicine.

Y chromosome haplogroup D2a1 is significantly associated with high levels of luteinizing hormone in Japanese men

T. Shinka, T. Iwamoto, Y. Nakahori, 2015, Andrology.