Lista de obras - Toshihiro Tanaka - Dominio Público Uruguay

A functional SNP in EDG2 increases susceptibility to knee osteoarthritis in Japanese

artículo científico publicado en 2008

A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction

A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population

artículo científico publicado en 2006

A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with lumbar-disc herniation

artículo científico publicado en 2008

A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis

artículo científico publicado en 2007

A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese

A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese

scientific journal article

A genome-wide association study identifies three new risk loci for Kawasaki disease

artículo científico publicado en 2012

A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation

artículo científico publicado en 2014

A high-throughput SNP typing system for genome-wide association studies

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

Alterations of gene expression during colorectal carcinogenesis revealed by cDNA microarrays after laser-capture microdissection of tumor tissues and normal epithelia.

artículo científico publicado en 2001

Association between maternal education and malocclusion in Mongolian adolescents: a cross-sectional study

artículo científico publicado en 2016

Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy

artículo científico publicado en 2002

Association of a single-nucleotide polymorphism in the immunoglobulin mu-binding protein 2 gene with immunoglobulin A nephropathy

artículo científico publicado en 2005

Association of an IGHV3-66 gene variant with Kawasaki disease

artículo científico publicado en 2020

Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients

artículo científico publicado en 2003

BRAP Activates Inflammatory Cascades and Increases the Risk for Carotid Atherosclerosis

artículo científico publicado en 2011

Cardiovascular genetics

artículo científico publicado en 2016

Characterization of S818L mutation in HERG C-terminus in LQT2. Modification of activation-deactivation gating properties

artículo científico publicado en 2000

Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations

artículo científico publicado en 2012

Common variants in CASP3 confer susceptibility to Kawasaki disease

artículo científico publicado en 2010

Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis

artículo científico publicado en 2008

Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese

artículo científico publicado en 2011

Complete sequencing and characterization of 21,243 full-length human cDNAs

artículo científico publicado en 2003

Correction to: Investigation of novel variations of ORAI1 gene and their association with Kawasaki disease

scientific article published on 01 October 2019

Correlation of genetic etiology with response to beta-adrenergic blockade among symptomatic patients with familial long-QT syndrome

artículo científico publicado en 2001

Decreased mortality associated with statin treatment in patients with acute myocardial infarction and lymphotoxin-alpha C804A polymorphism

Discovery and fine mapping of serum protein loci through transethnic meta-analysis

artículo científico publicado en 2012

Diverse transcriptional initiation revealed by fine, large-scale mapping of mRNA start sites

artículo científico publicado en 2001

Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data set

artículo científico publicado en 2016

Environmental factor dependent maximum likelihood method for association study targeted to personalized medicine

scientific article published on 01 January 2000

Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes

artículo científico publicado en 2015

Fine-scale SNP map of an 11-kb genomic region at 22q13.1 containing the galectin-1 gene

article

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome

artículo científico

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

artículo científico publicado en 2002

Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro

artículo científico publicado en 2004

Gene expression patterns as marker for 5-year postoperative prognosis of primary breast cancers.

artículo científico publicado en 2004

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

artículo científico

Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families.

artículo científico publicado en 1994

Genetic studies of body mass index yield new insights for obesity biology

artículo científico publicado en 2015

Genetic variations in five genes involved in the excitement of cardiomyocytes

artículo científico publicado en 2001

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes

artículo científico publicado en 2013

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

artículo científico publicado en 2013

Genome-wide association analysis of common genetic variants of resistant hypertension

scientific article published on 20 September 2018

Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus

Genome-wide association study identifies pharmacogenomic loci linked with specific antihypertensive drug treatment and new-onset diabetes.

scientific article published on 27 September 2016

Genome-wide association study to identify SNPs conferring risk of myocardial infarction and their functional analyses.

artículo científico publicado en 2005

Genome-wide association study to identify single-nucleotide polymorphisms conferring risk of myocardial infarction.

artículo científico publicado en 2006

Genome-wide detection and characterization of positive selection in human populations

artículo científico publicado en 2007

Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome

artículo científico publicado en 1998

Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome

artículo científico publicado en 1998

Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene

article

Growth and gene expression profile analyses of endometrial cancer cells expressing exogenous PTEN.

artículo científico publicado en 2001

Haplotypes with copy number and single nucleotide polymorphisms in CYP2A6 locus are associated with smoking quantity in a Japanese population

artículo científico publicado en 2012

Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population

artículo científico

High-density SNP map of human ITR, a gene associated with vascular remodeling

artículo científico publicado en 2003

High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2.

artículo científico publicado en 2001

Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias

artículo científico publicado en 2012

Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p.

artículo científico publicado en 1998

ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease

Identification and Characterization of the Potential Promoter Regions of 1031 Kinds of Human Genes

article

Identification by cDNA microarray of genes involved in ovarian carcinogenesis

article

Identification by differential display of eight known genes induced during in vivo intimal hyperplasia

artículo científico publicado en 1998

Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population

article

Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population

artículo científico publicado en 2000

Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21.

artículo científico publicado en 2003

Identification of AF17 as a downstream gene of the beta-catenin/T-cell factor pathway and its involvement in colorectal carcinogenesis

artículo científico

Identification of AXUD1, a novel human gene induced by AXIN1 and its reduced expression in human carcinomas of the lung, liver, colon and kidney

artículo científico publicado en 2001

Identification of a novel gene (ECM2) encoding a putative extracellular matrix protein expressed predominantly in adipose and female-specific tissues and its chromosomal localization to 9q22.3

artículo científico publicado en 1998

Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction

artículo científico publicado en 2006

Identification of nine novel loci associated with white blood cell subtypes in a Japanese population

artículo científico publicado en 2011

Identification of six new genetic loci associated with atrial fibrillation in the Japanese population.

artículo científico publicado en 2017

Identification of the gene responsible for gelatinous drop-like corneal dystrophy

artículo científico publicado en 1999

Identification of the interleukin 4 receptor alpha gene as a direct target for p73.

artículo científico

Induction of tenascin-C by tumor-specific EWS-ETS fusion genes

artículo científico publicado en 2003

Inflammation as a risk factor for myocardial infarction

artículo científico publicado en 2006

Inhibition of experimental intimal thickening in mice lacking a novel G-protein-coupled receptor

artículo científico publicado en 2003

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

artículo científico publicado en 2014

Investigation of novel variations of ORAI1 gene and their association with Kawasaki disease

article

Isolation and chromosomal mapping of the human homolog of perilipin (PLIN), a rat adipose tissue-specific gene, by differential display method

artículo científico publicado en 1998

Isolation of HELAD1, a novel human helicase gene up-regulated in colorectal carcinomas

artículo científico publicado en 2002

Isolation of a novel human gene, MARKL1, homologous to MARK3 and its involvement in hepatocellular carcinogenesis

artículo científico publicado en 2001

JSNP: a database of common gene variations in the Japanese population

artículo científico publicado en 2002

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

artículo científico publicado en 2017

Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits

artículo científico publicado en 2011

Linkage disequilibrium of evolutionarily conserved regions in the human genome

artículo científico publicado en 2006

Linkage of Familial Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis) to Chromosome 17q25

scientific article published on 01 April 2000

Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3

article

Mapping of a gene for May-Hegglin anomaly to chromosome 22q.

artículo científico publicado en 1999

Meta-analysis identifies common variants associated with body mass index in east Asians

artículo científico publicado en 2012

Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations

artículo científico publicado en 2012

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

artículo científico publicado en 2012

Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index

artículo científico publicado en 2014

Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci

artículo científico publicado en 2014

Molecular cloning and mapping of a human cDNA for cytosolic malate dehydrogenase (MDH1)

artículo científico publicado en 1996

Molecular cloning of a human cDNA encoding putative cysteine protease (PRSC1) and its chromosome assignment to 14q32.1.

artículo científico publicado en 1996

Molecular genetics of coronary artery disease

artículo científico

Multi-ethnic genome-wide association study for atrial fibrillation

article

Multiple loci are associated with white blood cell phenotypes

artículo científico publicado en 2011

Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians

artículo científico publicado en 2014

Multiple single-nucleotide polymorphisms (SNPs) in the Japanese population in six candidate genes for long QT syndrome

article

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome).

artículo científico publicado en 2001

Novel calmodulin mutations associated with congenital arrhythmia susceptibility

artículo científico publicado en 2014

Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese

artículo científico publicado en 2014

Novel mechanism of HERG current suppression in LQT2: shift in voltage dependence of HERG inactivation

artículo científico publicado en 1998

Osteopenia and male-specific sudden cardiac death in mice lacking a zinc transporter gene, Znt5.

artículo científico publicado en 2002

Prediction model for knee osteoarthritis based on genetic and clinical information

artículo científico publicado en 2010

Prediction of sensitivity of esophageal tumors to adjuvant chemotherapy by cDNA microarray analysis of gene-expression profiles.

artículo científico publicado en 2001

Recombination rates of genes expressed in human tissues

article

Reduced risk of recurrent myocardial infarction in homozygous carriers of the chromosome 9p21 rs1333049 C risk allele in the contemporary percutaneous coronary intervention era: a prospective observational study

artículo científico publicado en 2014

Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions

artículo científico publicado en 1995

Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese.

artículo científico publicado en 2018

Renin-Angiotensin-Aldosterone System Polymorphisms and 5-Year Mortality in Survivors of Acute Myocardial Infarction

artículo científico publicado en 2014

SNPs in BRAP associated with risk of myocardial infarction in Asian populations.

artículo científico publicado en 2009

SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population

artículo científico publicado en 2010

Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy

Small intestinal stem cell identity is maintained with functional Paneth cells in heterotopically grafted epithelium onto the colon

artículo científico publicado en 2014

Submicroscopic deletions at 13q32.1 cause congenital microcoria

artículo científico publicado en 2015

The Id2 gene is a novel target of transcriptional activation by EWS-ETS fusion proteins in Ewing family tumors.

artículo científico publicado en 2002

The p53 family member genes are involved in the Notch signal pathway

artículo científico publicado en 2002

Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population

article

Twenty single-nucleotide polymorphisms in four genes encoding cardiac ion channels

artículo científico publicado en 2002

Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome

artículo científico publicado en 2004

Voltage-shift of the current activation in HERG S4 mutation (R534C) in LQT2.

artículo científico publicado en 1999

p53DINP1, a p53-inducible gene, regulates p53-dependent apoptosis

scientific journal article

Lista de obras de Toshihiro Tanaka

A functional SNP in EDG2 increases susceptibility to knee osteoarthritis in Japanese

A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction

A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population

A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with lumbar-disc herniation

A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis

A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese

A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese

A genome-wide association study identifies three new risk loci for Kawasaki disease

A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation

A high-throughput SNP typing system for genome-wide association studies

A second generation human haplotype map of over 3.1 million SNPs

Alterations of gene expression during colorectal carcinogenesis revealed by cDNA microarrays after laser-capture microdissection of tumor tissues and normal epithelia.

Association between maternal education and malocclusion in Mongolian adolescents: a cross-sectional study

Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy

Association of a single-nucleotide polymorphism in the immunoglobulin mu-binding protein 2 gene with immunoglobulin A nephropathy

Association of an IGHV3-66 gene variant with Kawasaki disease

Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients

BRAP Activates Inflammatory Cascades and Increases the Risk for Carotid Atherosclerosis

Cardiovascular genetics

Characterization of S818L mutation in HERG C-terminus in LQT2. Modification of activation-deactivation gating properties

Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations

Common variants in CASP3 confer susceptibility to Kawasaki disease

Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis

Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese

Complete sequencing and characterization of 21,243 full-length human cDNAs

Correction to: Investigation of novel variations of ORAI1 gene and their association with Kawasaki disease

Correlation of genetic etiology with response to beta-adrenergic blockade among symptomatic patients with familial long-QT syndrome

Decreased mortality associated with statin treatment in patients with acute myocardial infarction and lymphotoxin-alpha C804A polymorphism

Discovery and fine mapping of serum protein loci through transethnic meta-analysis

Diverse transcriptional initiation revealed by fine, large-scale mapping of mRNA start sites

Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data set

Environmental factor dependent maximum likelihood method for association study targeted to personalized medicine

Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes

Fine-scale SNP map of an 11-kb genomic region at 22q13.1 containing the galectin-1 gene

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro

Gene expression patterns as marker for 5-year postoperative prognosis of primary breast cancers.

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families.

Genetic studies of body mass index yield new insights for obesity biology

Genetic variations in five genes involved in the excitement of cardiomyocytes

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Genome-wide association analysis of common genetic variants of resistant hypertension

Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus

Genome-wide association study identifies pharmacogenomic loci linked with specific antihypertensive drug treatment and new-onset diabetes.

Genome-wide association study to identify SNPs conferring risk of myocardial infarction and their functional analyses.

Genome-wide association study to identify single-nucleotide polymorphisms conferring risk of myocardial infarction.

Genome-wide detection and characterization of positive selection in human populations

Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome

Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome

Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene

Growth and gene expression profile analyses of endometrial cancer cells expressing exogenous PTEN.

Haplotypes with copy number and single nucleotide polymorphisms in CYP2A6 locus are associated with smoking quantity in a Japanese population

Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population

High-density SNP map of human ITR, a gene associated with vascular remodeling

High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2.

Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias

Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p.

ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease

Identification and Characterization of the Potential Promoter Regions of 1031 Kinds of Human Genes

Identification by cDNA microarray of genes involved in ovarian carcinogenesis

Identification by differential display of eight known genes induced during in vivo intimal hyperplasia

Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population

Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population

Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21.

Identification of AF17 as a downstream gene of the beta-catenin/T-cell factor pathway and its involvement in colorectal carcinogenesis

Identification of AXUD1, a novel human gene induced by AXIN1 and its reduced expression in human carcinomas of the lung, liver, colon and kidney

Identification of a novel gene (ECM2) encoding a putative extracellular matrix protein expressed predominantly in adipose and female-specific tissues and its chromosomal localization to 9q22.3

Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction

Identification of nine novel loci associated with white blood cell subtypes in a Japanese population

Identification of six new genetic loci associated with atrial fibrillation in the Japanese population.

Identification of the gene responsible for gelatinous drop-like corneal dystrophy

Identification of the interleukin 4 receptor alpha gene as a direct target for p73.

Induction of tenascin-C by tumor-specific EWS-ETS fusion genes

Inflammation as a risk factor for myocardial infarction

Inhibition of experimental intimal thickening in mice lacking a novel G-protein-coupled receptor

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation