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Noriyo Manabe

University of Tokyo

17

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611

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A Novel Synthetic Triazolotriazepine Derivative JTT-606 Inhibits Bone Resorption by Down-Regulation of Action and Production of Bone Resorptive Factors

2010 Journal of Bone and Mineral Research
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The ACVR1 617G>A mutation is also recurrent in three Japanese patients with fibrodysplasia ossificans progressiva

2007 Journal of Human Genetics
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Novel types of COMP mutations and genotype-phenotype association in pseudoachondroplasia and multiple epiphyseal dysplasia

2003 Human Genetics
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Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic form: Clinical course and phenotypic variations in four patients

2002 American Journal of Medical Genetics Part A
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Novel mutation in exon 18 of the cartilage oligomeric matrix protein gene causes a severe pseudoachondroplasia.

2001 American Journal of Medical Genetics
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Mutation in aging suppressor gene, Klotho, causes decreases in bone formation and resorption in mice

2000 Connective tissue
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Cellular and molecular mechanism of low-turnover osteopenia in the klotho-deficient mouse

2000 Cellular and Molecular Life Sciences
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Citations (34)
B-6 Analysis of FGFR3 mutation in achondroplasia-group bone dysplasia.

2000 Congenital Anomalies
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Independent impairment of osteoblast and osteoclast differentiation in klotho mouse exhibiting low-turnover osteopenia

1999 Journal of Clinical Investigation
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Citations (159)
Benign form of congenital angulation of long bones associated with shortening of soft tissues.

1998 Clinical Dysmorphology
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Citations (8)