Ikegawa Shiro | Laboratory Of Bone And Joint Diseases Center For Genomic Medicine

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著作論文

Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese
Lack of association of single nucleotide polymorphism in LRCH1 with knee osteoarthritis susceptibility
A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction
Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction
Distinct roles of Sox5, Sox6, and Sox9 in different stages of chondrogenic differentiation
High-resolution SNP map of ASPN, a susceptibility gene for osteoarthritis
A compound heterozygote of novel and recurrent DTDST mutations results in a novel intermediate phenotype of Desbuquois dysplasia, diastrophic dysplasia, and recessive form of multiple epiphyseal dysplasia
Association study of COL9A2 with lumbar disc disease in the Japanese population
Identification of novel RMRP mutations and specific founder haplotypes in Japanese patients with cartilage-hair hypoplasia
Nucleotide variations in genes encoding carbonic anhydrase 8 and 10 associated with femoral bone mineral density in Japanese female with osteoporosis
Association of genetic variations of genes encoding thrombospondin, type 1, domain-containing 4 and 7A with low bone mineral density in Japanese women with osteoporosis
Association of the aspartic acid-repeat polymorphism in the asporin gene with age at onset of knee osteoarthritis in Han Chinese Population
Replication of the association of the aspartic acid repeat polymorphism in the asporin gene with knee-osteoarthritis susceptibility in Han Chinese
Identification of sequence polymorphisms in CALM2 and analysis of association with hip osteoarthritis in a Japanese population
Cloning and characterization of the osteoarthritis-associated gene DVWA
Case-control association study between lumbar disc herniation
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population
SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese
A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia
TRPV4-pathy, a novel channelopathy affecting diverse systems

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