Search Results - "INOKO, HIDETOSHI"
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The HLA genomic loci map: expression, interaction, diversity and disease
Published in Journal of human genetics (01-01-2009)“…The human leukocyte antigen (HLA) super-locus is a genomic region in the chromosomal position 6p21 that encodes the six classical transplantation HLA genes and…”
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2
Comparative genomics of the human, macaque and mouse major histocompatibility complex
Published in Immunology (01-02-2017)“…Summary The MHC is a highly polymorphic genomic region that encodes the transplantation and immune regulatory molecules. It receives special attention for…”
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3
Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B51 and ERAP1
Published in Nature genetics (01-02-2013)“…Daniel Kastner and colleagues report genome-wide association analyses for Behçet's disease, a condition characterized by episodic inflammation of the skin and…”
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4
Genome-wide association studies identify IL23R - IL12RB2 and IL10 as Behçet's disease susceptibility loci
Published in Nature genetics (01-08-2010)“…Behçet's disease is a chronic systemic inflammatory disorder characterized by four major manifestations: recurrent ocular symptoms, oral and genital ulcers and…”
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High-risk HLA allele mismatch combinations responsible for severe acute graft-versus-host disease and implication for its molecular mechanism
Published in Blood (01-10-2007)“…In allogenic hematopoietic stem-cell transplantation, an effect of HLA locus mismatch in allele level on clinical outcome has been clarified. However, the…”
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Gene Map of the HLA Region, Graves' Disease and Hashimoto Thyroiditis, and Hematopoietic Stem Cell Transplantation
Published in Advances in immunology (2016)“…The human leukocyte antigen (HLA) genomic region spanning about 4 Mb is the most gene dense and the polymorphic stretches in the human genome. A total of the…”
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Genome-Wide Association Study in Asians Identifies Novel Loci for High Myopia and Highlights a Nervous System Role in Its Pathogenesis
Published in Ophthalmology (Rochester, Minn.) (01-12-2020)“…To identify novel susceptibility loci for high myopia. Genome-wide association study (GWAS) followed by replication and meta-analysis. A total of 14 096…”
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Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHD
Published in Blood (13-10-2016)“…Graft-versus-host disease (GVHD) is among the most challenging complications in unrelated donor hematopoietic cell transplantation (HCT). The highly…”
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Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease
Published in Proceedings of the National Academy of Sciences - PNAS (14-05-2013)“…Genome-wide association studies (GWAS) are a powerful means of identifying genes with disease-associated common variants, but they are not well-suited to…”
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10
Identification of HLA-DRB104:10 allele as risk allele for Japanese moyamoya disease and its association with autoimmune thyroid disease: A case-control study
Published in PloS one (14-08-2019)“…Moyamoya disease (MMD) is a progressive cerebrovascular disease with unknown etiology. Growing evidence suggest its involvement of autoimmune and genetic…”
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Current understanding of human genetics and genetic analysis of psoriasis
Published in Journal of dermatology (01-03-2012)“…During the past 5 years, genome‐wide association studies (GWAS), primarily based on single nucleotide polymorphism markers, have identified many loci as…”
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12
RAR-related orphan receptor A (RORA): A new susceptibility gene for multiple sclerosis
Published in Journal of the neurological sciences (15-10-2016)“…Abstract Retinoic acid receptor-related orphan receptor alpha (RORA) is proposed to promote Th17 cells differentiation that play a crucial role in many…”
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13
Which CIDE are you on? Apoptosis and energy metabolism
Published in Molecular bioSystems (01-01-2011)“…Around 1998, cell death-inducing DNA fragmentation factor-alpha (DFFA)-like effector (CIDE) proteins including CIDEA, CIDEB and CIDEC/fat specific protein 27…”
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14
Single nucleotide polymorphism detection by polymerase chain reaction-restriction fragment length polymorphism
Published in Nature protocols (01-11-2007)“…Accurate analysis of DNA sequence variation in not only humans and animals but also other organisms has played a significant role in expanding our knowledge…”
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15
Aggregation of rare/low-frequency variants of the mitochondria respiratory chain-related proteins in rheumatoid arthritis patients
Published in Journal of human genetics (01-08-2015)“…Exome sequencings were conducted using 59 patients having rheumatoid arthritis (RA) and 93 controls. After stepwise filtering, 107 genes showed less than 0.05…”
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16
Cost-efficient multiplex PCR for routine genotyping of up to nine classical HLA loci in a single analytical run of multiple samples by next generation sequencing
Published in BMC genomics (18-04-2015)“…HLA genotyping by next generation sequencing (NGS) requires three basic steps, PCR, NGS, and allele assignment. Compared to the conventional methods, such as…”
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HLA Association among Thai Patients with Diffuse and Limited Cutaneous Systemic Sclerosis
Published in Biomedicines (18-06-2024)“…This study aimed to clarify the association of HLA Class I and II with dcSSc and lcSSc in Thais. HLA typing for 11 gene loci (Class I: HLA-A, B and C, and…”
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Reference Grade Characterization of Polymorphisms in Full-Length HLA Class I and II Genes With Short-Read Sequencing on the ION PGM System and Long-Reads Generated by Single Molecule, Real-Time Sequencing on the PacBio Platform
Published in Frontiers in immunology (04-10-2018)“…Although NGS technologies fuel advances in high-throughput HLA genotyping methods for identification and classification of HLA genes to assist with precision…”
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Genetic variants on chromosome 1q41 influence ocular axial length and high myopia
Published in PLoS genetics (01-06-2012)“…As one of the leading causes of visual impairment and blindness, myopia poses a significant public health burden in Asia. The primary determinant of myopia is…”
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Major histocompatibility complex (Mhc) class Ib gene duplications, organization and expression patterns in mouse strain C57BL/6
Published in BMC genomics (17-04-2008)“…The mouse has more than 30 Major histocompatibility complex (Mhc) class Ib genes, most of which exist in the H2 region of chromosome 17 in distinct gene…”
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