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A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex DeficienciesNemo-like kinase suppresses a wide range of transcription factors, including nuclear factor-kappaBRare variant discovery by deep whole-genome sequencing of 1,070 Japanese individualsWRM-1 activates the LIT-1 protein kinase to transduce anterior/posterior polarity signals in C. elegansValidation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population.HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data.MiR-107 and MiR-185 can induce cell cycle arrest in human non small cell lung cancer cell lines.An efficient quantitation method of next-generation sequencing libraries by using MiSeq sequencer.Expression profiling in ovarian clear cell carcinoma: identification of hepatocyte nuclear factor-1 beta as a molecular marker and a possible molecular target for therapy of ovarian clear cell carcinomaEstablishment of Protocols for Global Metabolomics by LC-MS for Biomarker DiscoveryJaponica array: improved genotype imputation by designing a population-specific SNP array with 1070 Japanese individualsMammalian Nemo-like kinase enhances β-catenin-TCF transcription activity in human osteosarcoma and neuroblastoma cells.The structural origin of metabolic quantitative diversity.The Tohoku Medical Megabank Project: Design and Mission.Overexpression of cortactin is involved in motility and metastasis of hepatocellular carcinoma.Genome-wide identification of inter-individually variable DNA methylation sites improves the efficacy of epigenetic association studies.Identification of somatic genetic alterations in ovarian clear cell carcinoma with next generation sequencing.Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7.Evaluation of reported pathogenic variants and their frequencies in a Japanese population based on a whole-genome reference panel of 2049 individuals.Identification of somatic mutations in postmortem human brains by whole genome sequencing and their implications for psychiatric disorders.Construction of full-length Japanese reference panel of class I HLA genes with single-molecule, real-time sequencing.A Histologic Categorization of Aqueous Outflow Routes in Familial Open-Angle Glaucoma and Associations With Mutations in the MYOC Gene in Japanese Patients.Polymorphisms in the microglial marker molecule CX3CR1 affect the blood volume of the human brain.Clinicopathological significance of nuclear factor-κB activation in hepatocellular carcinoma.Gene expression profiles of cryopreserved CD34(+) human umbilical cord blood cells are related to their bone marrow reconstitution abilities in mouse xenografts.Development and application of a rapid and sensitive genotyping method for pharmacogene variants using the single-stranded tag hybridization chromatographic printed-array strip (STH-PAS)The genomic damage estimated by arbitrarily primed PCR DNA fingerprinting is useful for the prognosis of gastric cancerDetection of DNA Abnormalities by Arbitrarily Primed PCR Fingerprinting: Allelic Losses in Chromosome 10q in Lung CancersGenome analyses for the Tohoku Medical Megabank Project towards establishment of personalized healthcareConstruction of JRG (Japanese reference genome) with single-molecule real-time sequencing.Detection of DNA abnormalities by arbitrarily primed PCR fingerprinting: amplification of the MDM2 gene in a mediastinum fibrosarcomaMonitoring of minimal residual disease in early T-cell precursor acute lymphoblastic leukaemia by next-generation sequencingOmics research project on prospective cohort studies from the Tohoku Medical Megabank ProjectFunctional Characterization of 21 Allelic Variants of Dihydropyrimidine Dehydrogenase Identified in 1070 Japanese IndividualsA Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese IndividualsA single nucleotide polymorphism (-250 A/C) of the GFAP gene is associated with brain structures and cerebral blood flowRegional genetic differences among Japanese populations and performance of genotype imputation using whole-genome reference panel of the Tohoku Medical Megabank ProjectFunctional characterization of 40 CYP2B6 allelic variants by assessing efavirenz 8-hydroxylationIdentification of genetic alterations in extramammary Paget disease using whole exome analysisA low-frequency IL4R locus variant in Japanese patients with intravenous immunoglobulin therapy-unresponsive Kawasaki disease
P50
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P50
description
researcher
@en
name
Jun Yasuda
@en
Jun Yasuda
@nl
type
label
Jun Yasuda
@en
Jun Yasuda
@nl
prefLabel
Jun Yasuda
@en
Jun Yasuda
@nl
P106
P31
P496
0000-0002-3887-6871