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Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling

Nature communications, 2021-04, Vol.12 (1), p.2046-2046, Article 2046

2021

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Reduced dose of PTCy followed by adjuvant α-galactosylceramide enhances GVL effect without sacrificing GVHD suppression

Scientific reports, 2021-06, Vol.11 (1), p.13125-13125, Article 13125

2021

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Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction

Journal of human genetics, 2006-12, Vol.51 (12), p.1087-1099

2006

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Author Correction: 5-aminolevulinic acid-mediated photodynamic therapy can target aggressive adult T cell leukemia/lymphoma resistant to conventional chemotherapy

Scientific reports, 2021-03, Vol.11 (1), p.6420-6420, Article 6420

2021

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Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases

Nature genetics, 2020-07, Vol.52 (7), p.669-679

2020

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An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis

Nature genetics, 2005-02, Vol.37 (2), p.138-144

2005

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Post-transplantation cyclophosphamide restores early B-cell lymphogenesis that suppresses subsequent chronic graft-versus-host disease

Bone marrow transplantation (Basingstoke), 2021-04, Vol.56 (4), p.956-959

2021

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Pretransplant nivolumab further enhanced Treg expansion after posttransplant cyclophosphamide; another aspect for immune tolerance by PTCy after nivolumab

Leukemia, 2021-03, Vol.35 (3), p.929-931

2021

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5-aminolevulinic acid-mediated photodynamic therapy can target aggressive adult T cell leukemia/lymphoma resistant to conventional chemotherapy

Scientific reports, 2020-10, Vol.10 (1), p.17237-17237, Article 17237

2020

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A functional polymorphism in the 5′ UTR of GDF5 is associated with susceptibility to osteoarthritis

Nature genetics, 2007-04, Vol.39 (4), p.529-533

2007

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A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility

Nature genetics, 2010-06, Vol.42 (6), p.515-519

2010

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Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine

Nature genetics, 1998-07, Vol.19 (3), p.271-273

1998

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A functional SNP in CILP , encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease

Nature genetics, 2005-06, Vol.37 (6), p.607-612

2005

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A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population

Nature genetics, 2006-08, Vol.38 (8), p.921-925

2006

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Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis

Nature genetics, 2008-08, Vol.40 (8), p.994-998

2008

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SNPs in BRAP associated with risk of myocardial infarction in Asian populations

Nature genetics, 2009-03, Vol.41 (3), p.329-333

2009

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A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction

Journal of human genetics, 2007-03, Vol.52 (3), p.220-229

2007

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High-resolution SNP map of ASPN, a susceptibility gene for osteoarthritis

Journal of human genetics, 2006-02, Vol.51 (2), p.151-154

2006

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SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population

Journal of human genetics, 2011-01, Vol.56 (1), p.47-51

2011

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Cloning and characterization of human and mouse PROSC (proline synthetase co-transcribed) genes

Journal of human genetics, 1999-01, Vol.44 (5), p.337-342

1999

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An autosomal dominant posterior polar cataract locus maps to human chromosome 20p12-q12

European journal of human genetics : EJHG, 2000-07, Vol.8 (7), p.535-539

2000

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Dinucleotide repeat polymorphism on chromosome 9q32

Journal of human genetics, 1995-12, Vol.40 (4), p.333-334

1995

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The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32

Journal of human genetics, 1998-02, Vol.43 (1), p.32-36

1998

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Genomic organization, mapping, and polymorphisms of the gene encoding human cartilage intermediate layer protein (CILP)

Journal of human genetics, 1999-01, Vol.44 (3), p.203-205

1999

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An autosomal dominant posterior polar cataract locus maps to human chromosome20p12-q12

European journal of human genetics : EJHG, 2000-07, Vol.8 (7), p.535-539

2000

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Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling

Reduced dose of PTCy followed by adjuvant α-galactosylceramide enhances GVL effect without sacrificing GVHD suppression

Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction

Author Correction: 5-aminolevulinic acid-mediated photodynamic therapy can target aggressive adult T cell leukemia/lymphoma resistant to conventional chemotherapy

Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases

An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis

Post-transplantation cyclophosphamide restores early B-cell lymphogenesis that suppresses subsequent chronic graft-versus-host disease

Pretransplant nivolumab further enhanced Treg expansion after posttransplant cyclophosphamide; another aspect for immune tolerance by PTCy after nivolumab

5-aminolevulinic acid-mediated photodynamic therapy can target aggressive adult T cell leukemia/lymphoma resistant to conventional chemotherapy

A functional polymorphism in the 5′ UTR of GDF5 is associated with susceptibility to osteoarthritis

A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility

Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine

A functional SNP in CILP , encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease

A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population

Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis

SNPs in BRAP associated with risk of myocardial infarction in Asian populations

A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction

High-resolution SNP map of ASPN, a susceptibility gene for osteoarthritis

SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population

Cloning and characterization of human and mouse PROSC (proline synthetase co-transcribed) genes

An autosomal dominant posterior polar cataract locus maps to human chromosome 20p12-q12

Dinucleotide repeat polymorphism on chromosome 9q32

The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32

Genomic organization, mapping, and polymorphisms of the gene encoding human cartilage intermediate layer protein (CILP)

An autosomal dominant posterior polar cataract locus maps to human chromosome20p12-q12

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