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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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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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

2006

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Dinucleotide repeat polymorphism on chromosome 9q32

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

1995

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

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

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

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

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

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

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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