Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus
暂无分享,去创建一个
Yusuke Nakamura | Tatsuhiko Tsunoda | Masafumi Matsuda | Kohei Kaku | Mark Walker | Naoyuki Kamatani | Daisuke Koya | Ryuzo Kawamori | Yasuhiko Iwamoto | Takashi Eguchi | Hiroshi Maegawa | Hiroshi Hirose | Yasushi Tanaka | M. McCarthy | A. Hattersley | G. Hitman | M. Walker | C. Groves | Yusuke Nakamura | A. Sekine | T. Tsunoda | M. Matsuda | N. Kamatani | T. Fujioka | Y. Iwamoto | H. Maegawa | R. Kawamori | A. Kashiwagi | D. Koya | R. Kikkawa | S. Maeda | H. Hirose | K. Kaku | Yasushi Tanaka | Atsunori Kashiwagi | Tomoaki Fujioka | Shiro Maeda | Tetsuya Babazono | Ryuichi Kikkawa | Akihiro Sekine | T. Babazono | Akio Kanazawa | A. Kanazawa | Shuichi Tsukada | Yoichi Ohno | Christopher J. Groves | Andrew T. Hattersley | Graham A. Hitman | Mark I. McCarthy | T. Eguchi | S. Tsukada | Y. Ohno | M. McCarthy | M. McCarthy
[1] Yusuke Nakamura,et al. Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis , 2003, Nature Genetics.
[2] M. McCarthy,et al. Association and haplotype analysis of the insulin-degrading enzyme (IDE) gene, a strong positional and biological candidate for type 2 diabetes susceptibility. , 2003, Diabetes.
[3] Yusuke Nakamura,et al. Functional haplotypes of PADI 4 , encoding citrullinating enzyme peptidylarginine deiminase 4 , are associated with rheumatoid arthritis , 2003 .
[4] Scott M. Williams,et al. Genotyping of essential hypertension single-nucleotide polymorphisms by a homogeneous PCR method with universal energy transfer primers. , 2002, Clinical chemistry.
[5] Hiroshi Sato,et al. Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction , 2002, Nature Genetics.
[6] Yusuke Nakamura,et al. Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190 562 genetic variations in the human genome , 2002, Journal of Human Genetics.
[7] D. Clayton,et al. A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes. , 2002, American journal of human genetics.
[8] Yusuke Nakamura,et al. JSNP: a database of common gene variations in the Japanese population , 2002, Nucleic Acids Res..
[9] J. Shaw,et al. Global and societal implications of the diabetes epidemic , 2001, Nature.
[10] M. Daly,et al. High-resolution haplotype structure in the human genome , 2001, Nature Genetics.
[11] G I Bell,et al. Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young. , 2001, The New England journal of medicine.
[12] R Foxon,et al. A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q. , 2001, American journal of human genetics.
[13] A. Sekine,et al. Identification of 197 genetic variations in six human methyltransferase genes in the Japanese population , 2001, Journal of Human Genetics.
[14] Yusuke Nakamura,et al. A high-throughput SNP typing system for genome-wide association studies , 2001, Journal of Human Genetics.
[15] Y. Ohnishi,et al. Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibility to the disease. , 2001, American journal of human genetics.
[16] A. Saltiel. New Perspectives into the Molecular Pathogenesis and Treatment of Type 2 Diabetes , 2001, Cell.
[17] J. V. Moran,et al. Initial sequencing and analysis of the human genome. , 2001, Nature.
[18] International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome , 2001, Nature.
[19] Tom H. Lindner,et al. Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus , 2000, Nature Genetics.
[20] M. Daly,et al. Guilt by association , 2000, Nature Genetics.
[21] Yusuke Nakamura,et al. Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene , 2000, Journal of Human Genetics.
[22] Eric S. Lander,et al. The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes , 2000, Nature Genetics.
[23] S. Kihara,et al. Genomic structure and mutations in adipose-specific gene, adiponectin , 2000, International Journal of Obesity.
[24] B. Gelb,et al. Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus , 2000, Nature Genetics.
[25] T. Funahashi,et al. Molecular Mechanism of Metabolic Syndrome X: Contribution of Adipocytokines · Adipocyte‐derived Bioactive Substances , 1999, Annals of the New York Academy of Sciences.
[26] J. Todd,et al. The insulin gene VNTR, type 2 diabetes and birth weight , 1999, Nature Genetics.
[27] B. Kahn. Type 2 Diabetes: When Insulin Secretion Fails to Compensate for Insulin Resistance , 1998, Cell.
[28] Takuji Nishimura,et al. Mersenne twister: a 623-dimensionally equidistributed uniform pseudo-random number generator , 1998, TOMC.
[29] K. Zerres,et al. Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2beta. , 1997, Genes & development.
[30] B. Spiegelman,et al. Adipogenesis and Obesity: Rounding Out the Big Picture , 1996, Cell.
[31] L. Abraham,et al. Identification of an AP‐2 element in the ‐323 to ‐285 region of the TNF‐α gene , 1996 .
[32] L. Abraham,et al. Identification of an AP-2 element in the -323 to -285 region of the TNF-alpha gene. , 1996, Biochemistry and molecular biology international.
[33] K. Nakao,et al. Structural Organization and Chromosomal Assignment of the Human obese Gene (*) , 1995, The Journal of Biological Chemistry.
[34] R. Schüle,et al. Cloning and characterization of a second AP-2 transcription factor: AP-2 beta. , 1995, Development.
[35] L. Excoffier,et al. Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population. , 1995, Molecular biology and evolution.
[36] R. Sakuta,et al. A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA. , 1994, The New England journal of medicine.