Hidetoshi Inoko focuses on Genetics, Gene, Human leukocyte antigen, Immunology and Allele. Major histocompatibility complex, Haplotype, Locus, MHC class I and Linkage disequilibrium are the subjects of his Genetics studies. His Haplotype course of study focuses on Genetic variation and Evolutionary biology.
His study in Molecular biology extends to Gene with its themes. His Human leukocyte antigen research incorporates elements of Allele frequency, Leukemia, Genetic predisposition and Transplantation. His Immunology study integrates concerns from other disciplines, such as Internal medicine, Behcet's disease, Disease and Genotyping.
Hidetoshi Inoko spends much of his time researching Genetics, Human leukocyte antigen, Allele, Immunology and Gene. Many of his studies involve connections with topics such as Molecular biology and Genetics. The various areas that he examines in his Human leukocyte antigen study include Internal medicine, Transplantation and Typing.
His work carried out in the field of Allele brings together such families of science as Genotyping, Genotype and Single-nucleotide polymorphism. His research integrates issues of Restriction fragment length polymorphism and Polymerase chain reaction in his study of Genotyping. His biological study spans a wide range of topics, including Hematopoietic stem cell transplantation, Behcet's disease and Disease.
His scientific interests lie mostly in Genetics, Human leukocyte antigen, Immunology, Allele and Haplotype. His Human leukocyte antigen study also includes fields such as
His Allele research is multidisciplinary, incorporating elements of Histocompatibility Testing and Autism. Haplotype is a primary field of his research addressed under Gene. His Gene study frequently links to related topics such as Molecular biology.
Hidetoshi Inoko mainly investigates Genetics, Human leukocyte antigen, Immunology, Genome-wide association study and Single-nucleotide polymorphism. His Genetics study is mostly concerned with Genetic association, Locus, Genotype, Genotyping and Haplotype. His Haplotype research is classified as research in Gene.
Hidetoshi Inoko interconnects Allele and Transplantation in the investigation of issues within Human leukocyte antigen. The concepts of his Allele study are interwoven with issues in Multiple sclerosis and Endocrinology. His Single-nucleotide polymorphism research is multidisciplinary, incorporating perspectives in Psoriasis and Behcet's disease, Disease.
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Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution
Ladeana W. Hillier;Webb Miller;Ewan Birney;Wesley Warren.
Complete sequence and gene map of a human major histocompatibility complex
S Beck;D Geraghty;H Inoko;L Rowen.
Effect of matching of class I HLA alleles on clinical outcome after transplantation of hematopoietic stem cells from an unrelated donor
Takehiko Sasazuki;Takeo Juji;Yasuo Morishima;Naoko Kinukawa.
The New England Journal of Medicine (1998)
The clinical significance of human leukocyte antigen (HLA) allele compatibility in patients receiving a marrow transplant from serologically HLA-A, HLA-B, and HLA-DR matched unrelated donors.
Yasuo Morishima;Takehiko Sasazuki;Hidetoshi Inoko;Takeo Juji.
The HLA genomic loci map: expression, interaction, diversity and disease
Takashi Shiina;Kazuyoshi Hosomichi;Hidetoshi Inoko;Jerzy K Kulski;Jerzy K Kulski.
Journal of Human Genetics (2009)
The amphioxus genome illuminates vertebrate origins and cephalochordate biology
Linda Z. Holland;Ricard Albalat;Kaoru Azumi;Èlia Benito-Gutiérrez.
Genome Research (2008)
Genome-wide association studies identify IL23R - IL12RB2 and IL10 as Behçet's disease susceptibility loci
Nobuhisa Mizuki;Akira Meguro;Masao Ota;Shigeaki Ohno.
Nature Genetics (2010)
Mapping human genetic diversity in Asia
Mahmood Ameen Abdulla;Ikhlak Ahmed;Anunchai Assawamakin;Anunchai Assawamakin;Jong Bhak.
Triplet repeat polymorphism in the transmembrane region of the MICA gene: A strong association of six GCT repetitions with Behçet disease
Nobuhisa Mizuki;Masao Ota;Minoru Kimura;Shigeaki Ohno.
Proceedings of the National Academy of Sciences of the United States of America (1997)
Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1
Yohei Kirino;George Bertsias;George Bertsias;Yoshiaki Ishigatsubo;Nobuhisa Mizuki.
Nature Genetics (2013)
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