Sadahiko Iwamoto

Ontology type: schema:Person     

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Publications in SciGraph latest 50 shown

  • 2022-09-28 Probiotics suppress nonalcoholic steatohepatitis and carcinogenesis progression in hepatocyte-specific PTEN knockout mice in SCIENTIFIC REPORTS
  • 2022-08-19 Genome-wide DNA methylation status of Mongolians exhibits signs of cellular stress response related to their nomadic lifestyle in JOURNAL OF PHYSIOLOGICAL ANTHROPOLOGY
  • 2021-04-16 ILDR2 stabilization is regulated by its interaction with GRP78 in SCIENTIFIC REPORTS
  • 2017-09-26 Identification of deleterious rare variants in MTTP, PNPLA3, and TM6SF2 in Japanese males and association studies with NAFLD in LIPIDS IN HEALTH AND DISEASE
  • 2017-02-17 An adaptive variant of TRIB2, rs1057001, is associated with higher expression levels of thermogenic genes in human subcutaneous and visceral adipose tissues in JOURNAL OF PHYSIOLOGICAL ANTHROPOLOGY
  • 2016-01-13 Replication analysis of genetic association of the NCAN-CILP2 region with plasma lipid levels and non-alcoholic fatty liver disease in Asian and Pacific ethnic groups in LIPIDS IN HEALTH AND DISEASE
  • 2015-03-13 The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis in MOLECULAR AUTISM
  • 2014-12-22 Seasonal effects of the UCP3 and the RPTOR gene polymorphisms on obesity traits in Japanese adults in JOURNAL OF PHYSIOLOGICAL ANTHROPOLOGY
  • 2012-12-11 A functional SNP upstream of the beta-2 adrenergic receptor gene (ADRB2) is associated with obesity in Oceanic populations in INTERNATIONAL JOURNAL OF OBESITY
  • 2012-10-31 Positive natural selection of TRIB2, a novel gene that influences visceral fat accumulation, in East Asia in HUMAN GENETICS
  • 2012-05-29 Association of CTXN3-SLC12A2 polymorphisms and schizophrenia in a Thai population in BEHAVIORAL AND BRAIN FUNCTIONS
  • 2011-09-22 High prevalence of an anti-hypertriglyceridemic variant of the MLXIPL gene in Central Asia in JOURNAL OF HUMAN GENETICS
  • 2011-07-21 OPCML Gene as a Schizophrenia Susceptibility Locus in Thai Population in JOURNAL OF MOLECULAR NEUROSCIENCE
  • 2010-04-03 A single nucleotide polymorphism in the FADS1/FADS2 gene is associated with plasma lipid profiles in two genetically similar Asian ethnic groups with distinctive differences in lifestyle in HUMAN GENETICS
  • 2007-07 Are Promoter Polymorphisms of Interleukin 6 Ready to Be Applied in Genetic Markers of Cardiovascular Diseases? in HYPERTENSION RESEARCH
  • 2006-09-28 Identification of a regulatory SNP in the retinol binding protein 4 gene associated with type 2 diabetes in Mongolia in HUMAN GENETICS
  • 2006-07-26 An intronic variable number of tandem repeat polymorphisms of the cold-induced autoinflammatory syndrome 1 (CIAS1) gene modifies gene expression and is associated with essential hypertension in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2000-05-01 A Japanese propositus with D-- phenotype characterized by the deletion of both the RHCE gene and D1S80 locus situated in chromosome 1p and the existence of a new CE-D-CE hybrid gene in JOURNAL OF HUMAN GENETICS
  • 1999-10 Deletion of A-antigen in a human cancer cell line is associated with reduced promoter activity of CBF/NF-Y binding region, and possibly with enhanced DNA methylation of A transferase promoter in GLYCOCONJUGATE JOURNAL
  • 1999-05 The STR polymorphisms in intron 8 may provide information about the molecular evolution of RH haplotypes in HUMAN GENETICS
  • 1998-09-01 A novel missense mutation of the tissue-nonspecific alkaline phosphatase gene detected in a patient with hypophosphatasia in JOURNAL OF HUMAN GENETICS
  • 1998 Expression analysis of human Rhesus blood group antigens by gene transduction into erythroid and non-erythroid cells. in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 1997-04 Dinucleotide repeat in the 3′ flanking region provides a clue to the molecular evolution of the Duffy gene in HUMAN GENETICS
  • 1997 Identification of the truncated Duffy mRNAs in erythroid cells. in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 1994 Further Evidence for Transformation of Genetic Markers in Recipients after BMT in ADVANCES IN FORENSIC HAEMOGENETICS
  • 1993-03 Isolation of a new cDNA clone encoding an Rh polypeptide associated with the Rh blood group system in HUMAN GENETICS
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