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Comparative Metagenomics Revealed Commonly Enriched Gene Sets in Human Gut Microbiomes

DNA research, 2007-01, Vol.14 (4), p.169-181

2007

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Unique activation status of peripheral blood mononuclear cells at acute phase of Kawasaki disease

Clinical and experimental immunology, 2010-05, Vol.160 (2), p.246-255

2010

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Chronic Granulomatous Disease: Two Decades of Experience From a Tertiary Care Centre in North West India

Journal of clinical immunology, 2014, Vol.34 (1), p.58-67

2014

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DIAGNOSTIC UTILITY OF ALDEHYDE DEGRADATION DEFICIENCY SYNDROME USING PROTEOMIC ANALYSIS

Leukemia research reports, 2024, Vol.21, p.100418, Article 100418

2024

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A nationwide survey of Aicardi-Goutieres syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study

Rheumatology (Oxford, England), 2014-03, Vol.53 (3), p.448-458

2014

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OP0120 Roles of B Cell Leukemia/Lymphoma 3 in The Development of T Follicular Helper Cells and the Pathogenesis of Rheumatoid Arthritis

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.113-114

2015

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Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency

Haematologica (Roma), 2007-12, Vol.92 (12), p.e123-e125

2007

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Exploration of Human ORFeome: High-Throughput Preparation of ORF Clones and Efficient Characterization of Their Protein Products

DNA research, 2008-06, Vol.15 (3), p.137-149

2008

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Directional cDNA library construction assisted by the in vitro recombination reaction

Nucleic acids research, 2001-02, Vol.29 (4), p.E22-22

2001

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RAPID: Resource of Asian Primary Immunodeficiency Diseases

Nucleic acids research, 2009-01, Vol.37 (Database issue), p.D863-D867

2009

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FRI0007 Prediction of Therapeutic Responses to TOCILIZUMAB in Patients with Rheumatoid Arthritis Using Biomarkers Identified by Genome-Wide DNA Microarray Analysis in Peripheral Blood Mononuclear Cells

Annals of the rheumatic diseases, 2014-06, Vol.73 (Suppl 2), p.383-383

2014

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Integrated hydrophilic surface treatment system of vapor deposition polymerization and vacuum ultraviolet irradiation for chemical/biochemical microchips

Microelectronic engineering, 2011-08, Vol.88 (8), p.2751-2754

2011

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Analysis of Mutations in the IL2RG Gene in 2 Asian Infants With X-linked Severe Combined Immunodeficiency

Journal of investigational allergology & clinical immunology, 2015-01, Vol.25 (4), p.313-315

2015

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Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro

DNA research, 2000-04, Vol.7 (2), p.143-150

2000

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FRI0208 Prediction of treatment response of tocilizumab for rheumatoid arthritis with comprehensive gene expression analysis in peripheral blood mononuclear cells

Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.384-384

2013

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Molecular cloning of pancreatic group I phospholipase A2 receptor

The Journal of biological chemistry, 1994-02, Vol.269 (8), p.5897-5904

1994

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Transcriptome Analysis of a cDNA Library from Adult Human Epididymis

DNA research, 2008-06, Vol.15 (3), p.115-122

2008

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Plasmacytoid Dendritic Cells Are Crucial for the Initiation of Inflammation and T Cell Immunity In Vivo

Immunity (Cambridge, Mass.), 2011-12, Vol.35 (6), p.958-971

2011

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XPS and NEXAFS studies of VUV/O₃-treated aromatic polyurea and its application to microchip electrophoresis

IET nanobiotechnology, 2011-12, Vol.5 (4), p.136-142

2011

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Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome

Journal of investigational allergology & clinical immunology, 2010, Vol.20 (5), p.442-445

2010

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Remarkable improvement of articular pain by biologics in a Multicentric carpotarsal osteolysis patient with a mutation of MAFB gene

Pediatric rheumatology online journal, 2015-09, Vol.13 (Suppl 1), p.P152-P152, Article P152

2015

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Successful treatment of systemic cytomegalovirus infection in severe combined immunodeficiency using allogeneic bone marrow transplantation followed by adoptive immunotherapy

Journal of investigational allergology & clinical immunology, 2014, Vol.24 (3), p.200-202

2014

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Hyper IgM syndrome and complement Clq deficiency in an individual with systemic lupus erythematosus-like disease

Clinical and experimental rheumatology, 2010-07, Vol.28 (4), p.558

2010

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Neurofilament Deficiency in Quail Caused by Nonsense Mutation in Neurofilament-L Gene

The Journal of cell biology, 1993-04, Vol.121 (2), p.387-395

1993

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IκB kinase-α is critical for interferon-α production induced by Toll-like receptors 7 and 9

Nature, 2006-04, Vol.440 (7086), p.949-953

2006

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Comparative Metagenomics Revealed Commonly Enriched Gene Sets in Human Gut Microbiomes

Unique activation status of peripheral blood mononuclear cells at acute phase of Kawasaki disease

Chronic Granulomatous Disease: Two Decades of Experience From a Tertiary Care Centre in North West India

DIAGNOSTIC UTILITY OF ALDEHYDE DEGRADATION DEFICIENCY SYNDROME USING PROTEOMIC ANALYSIS

A nationwide survey of Aicardi-Goutieres syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study

OP0120 Roles of B Cell Leukemia/Lymphoma 3 in The Development of T Follicular Helper Cells and the Pathogenesis of Rheumatoid Arthritis

Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency

Exploration of Human ORFeome: High-Throughput Preparation of ORF Clones and Efficient Characterization of Their Protein Products

Directional cDNA library construction assisted by the in vitro recombination reaction

RAPID: Resource of Asian Primary Immunodeficiency Diseases

FRI0007 Prediction of Therapeutic Responses to TOCILIZUMAB in Patients with Rheumatoid Arthritis Using Biomarkers Identified by Genome-Wide DNA Microarray Analysis in Peripheral Blood Mononuclear Cells

Integrated hydrophilic surface treatment system of vapor deposition polymerization and vacuum ultraviolet irradiation for chemical/biochemical microchips

Analysis of Mutations in the IL2RG Gene in 2 Asian Infants With X-linked Severe Combined Immunodeficiency

Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro

FRI0208 Prediction of treatment response of tocilizumab for rheumatoid arthritis with comprehensive gene expression analysis in peripheral blood mononuclear cells

Molecular cloning of pancreatic group I phospholipase A2 receptor

Transcriptome Analysis of a cDNA Library from Adult Human Epididymis

Plasmacytoid Dendritic Cells Are Crucial for the Initiation of Inflammation and T Cell Immunity In Vivo

XPS and NEXAFS studies of VUV/O₃-treated aromatic polyurea and its application to microchip electrophoresis

Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome

Remarkable improvement of articular pain by biologics in a Multicentric carpotarsal osteolysis patient with a mutation of MAFB gene

Successful treatment of systemic cytomegalovirus infection in severe combined immunodeficiency using allogeneic bone marrow transplantation followed by adoptive immunotherapy

Hyper IgM syndrome and complement Clq deficiency in an individual with systemic lupus erythematosus-like disease

Neurofilament Deficiency in Quail Caused by Nonsense Mutation in Neurofilament-L Gene

IκB kinase-α is critical for interferon-α production induced by Toll-like receptors 7 and 9

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