Search Results1-20 of  28

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  • Ikegawa Shiro ID: 9000345445655

    Articles in CiNii:1

    • Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasia (2017)
  • Ikegawa Shiro ID: 9000345445701

    Articles in CiNii:1

    • Novel and recurrent XYLT1 mutations in two Turkish families with Desbuquois dysplasia, type 2 (2017)
  • Ikegawa Shiro ID: 9000356596926

    Articles in CiNii:1

    • Axial spondylometaphyseal dysplasia is also caused by NEK1 mutations (2017)
  • IKEGAWA Shiro ID: 9000001076275

    Laboratory of Bone and Joint Diseases, Center for Genomic Medicine (2012 from CiNii)

    Articles in CiNii:25

    • Genomic organization, mapping, and polymorphisms of the gene encoding human cartilage intermediate layer protein (CILP) (1999)
    • Identification of sequence polymorphisms of the COMP (cartilage oligomeric matrix protein) gene and association study in osteoarthrosis of the knee and hip joints (2001)
    • Identification of sequence polymorphisms in two sulfation-related genes, PAPSS2 and SLC26A2, and an association analysis with knee osteoarthritis (2001)
  • IKEGAWA Shiro ID: 9000001076686

    Laboratory of Genome Medicine, Institute of Medical Science, Human Genome Center, University of Tokyo (1999 from CiNii)

    Articles in CiNii:1

    • Cloning and characterization of human and mouse PROSC (proline synthetase co-transcribed) genes (1999)
  • IKEGAWA Shiro ID: 9000001362026

    Laboratory of Molecular Medicine, Institute of Medical Science, The University of Tokyo (1995 from CiNii)

    Articles in CiNii:1

    • DINUCLEOTIDE REPEAT POLYMORPHISM ON CHROMOSOME 9q32 (1995)
  • IKEGAWA Shiro ID: 9000001557906

    Human Genome Center, Institute of Medical Science, University of Tokyo (1998 from CiNii)

    Articles in CiNii:1

    • The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32 (1998)
  • IKEGAWA Shiro ID: 9000001788511

    Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN (2006 from CiNii)

    Articles in CiNii:1

    • Genetic analysis of skeletal dysplasia : recent advances and perspectives in the post-genome-sequence era (2006)
  • IKEGAWA Shiro ID: 9000002065990

    Laboratory for Bone and Joint Disease, SNP Research Center, RIKEN, Institute of Medical Science, University of Tokyo (2006 from CiNii)

    Articles in CiNii:1

    • Clinical and Genetic Analyses of Presumed Shwachman-Diamond Syndrome in Japan (2006)
  • IKEGAWA Shiro ID: 9000018236637

    Laboratory for Bone and Joint Diseases, Center for Genomic Medicine (2010 from CiNii)

    Articles in CiNii:1

    • Binding characteristics of the osteoarthritis-associated protein asporin (2010)
  • IKEGAWA Shiro ID: 9000018697372

    Department of Orthopedics, The University of Tokyo (1996 from CiNii)

    Articles in CiNii:1

    • THERMOGRAPHIC OBSERVATIONS IN PATIENTS WITH OBSTETRIC PARALYSIS (1996)
  • IKEGAWA Shiro ID: 9000019183236

    Laboratory for Bone and Joint Diseases, Center for Genomic Medicine (2011 from CiNii)

    Articles in CiNii:1

    • Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriers (2011)
  • IKEGAWA Shiro ID: 9000019188147

    Laboratory for Bone and Joint Diseases, Center for Genomic Medicine (2010 from CiNii)

    Articles in CiNii:1

    • Recent advances in association studies of osteoarthritis susceptibility genes (2010)
  • IKEGAWA Shiro ID: 9000256893553

    Laboratory for Bone and Joint Diseases, Center for Genomic Medicine (2013 from CiNii)

    Articles in CiNii:1

    • Association of the formiminotransferase N-terminal sub-domain containing gene and thrombospondin, type 1, domain-containing 7A gene with the prevalence of vertebral fracture in 2427 consecutive autopsy cases (2013)
  • IKEGAWA Shiro ID: 9000259324999

    Laboratory of Bone and Joint Diseases, Center for Genomic Medicine (2013 from CiNii)

    Articles in CiNii:1

    • A Replication Study for Association of 5 Single Nucleotide Polymorphisms With Curve Progression of Adolescent Idiopathic Scoliosis in Japanese Patients (2013)
  • IKEGAWA Shiro ID: 9000259330830

    Laboratory for Bone and Joint Diseases, Center for Genomic Medicine, RIKEN (2013 from CiNii)

    Articles in CiNii:1

    • A genome-wide sib-pair linkage analysis of ossification of the posterior longitudinal ligament of the spine (2013)
  • IKEGAWA Shiro ID: 9000261672895

    Laboratory for Bone and Joint Diseases, Center for Genomic Medicine (2013 from CiNii)

    Articles in CiNii:1

    • Exome sequencing identifies a novel INPPL1 mutation in opsismodysplasia (2013)
  • IKEGAWA Shiro ID: 9000272993631

    Laboratory for Bone and Joint Diseases, RIKEN Center for Integrative Medical Sciences (2014 from CiNii)

    Articles in CiNii:1

    • Genomic study of ossification of the posterior longitudinal ligament of the spine (2014)
  • IKEGAWA Shiro ID: 9000350653449

    Laboratory for Bone and Joint Diseases, RIKEN Center for Integrative Medical Sciences, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan (2017 from CiNii)

    Articles in CiNii:1

    • An ENU-induced p.C225S missense mutation in the mouse <i>Tgfb1</i> gene does not cause Camurati-Engelmann disease-like skeletal phenotypes (2017)
  • Ikegawa Shiro ID: 9000238293898

    Articles in CiNii:1

    • Human Genetic Disorders Caused by Mutations in Genes Encoding Biosynthetic Enzymes for Sulfated Glycosaminoglycans (2013)
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