N. Manabe

发表

Independent impairment of osteoblast and osteoclast differentiation in klotho mouse exhibiting low-turnover osteopenia.

M. Kuro-o, H. Kawaguchi, K. Nakamura, 1999, The Journal of clinical investigation.

Connection Between B Lymphocyte and Osteoclast Differentiation Pathways1

Kozo Nakamura, R. Scheuermann, Y. Nabeshima, 2001, The Journal of Immunology.

Involvement of fibroblast growth factor-2 in joint destruction of rheumatoid arthritis patients.

K. Nakamura, H. Oda, N. Manabe, 1999, Rheumatology.

Osteoclast Differentiation Pathways Connection Between B Lymphocyte and

Kozo Nakamura, H. Kawaguchi, Y. Nabeshima, 2001 .

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

M. Kuro-o, H. Kawaguchi, K. Nakamura, 2000, Cellular and Molecular Life Sciences CMLS.

A mild form of pseudoachondroplasia: minimal epi-metaphyseal involvement of long bones.

S. Ikegawa, M. Kimizuka, K. Nakamura, 1998, European journal of radiology.

Novel types of COMP mutations and genotype-phenotype association in pseudoachondroplasia and multiple epiphyseal dysplasia

Kozo Nakamura, N. Brunetti‐Pierri, H. Ohashi, 2002, Human Genetics.

Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasia

R. Kosaki, H. Ohashi, S. Ikegawa, 2004, Human mutation.

Swelling of the dorsum of the hand and/or foot can be a first sign of Maffucci syndrome

T. Ishida, N. Haga, T. Matsushita, 1999, Archives of Orthopaedic and Trauma Surgery.

The ACVR1 617G>A mutation is also recurrent in three Japanese patients with fibrodysplasia ossificans progressiva

M. Nakajima, S. Ikegawa, N. Haga, 2007, Journal of Human Genetics.

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

Kozo Nakamura, T. Takato, H. Kawaguchi, 2000, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Stature and severity in multiple epiphyseal dysplasia.

S. Ikegawa, N. Haga, M. Kimizuka, 1998, Journal of pediatric orthopedics.

Novel mutation in exon 18 of the cartilage oligomeric matrix protein gene causes a severe pseudoachondroplasia.

S. Ikegawa, N. Haga, A. Mabuchi, 2001, American journal of medical genetics.

Additive effects of combined treatment with etidronate and alfacalcidol on bone mass and mechanical properties in ovariectomized rats.

H. Kawaguchi, H Kawaguchi, T. Katsumata, 2000, Bone.

Benign form of congenital angulation of long bones associated with shortening of soft tissues

Kozo Nakamura, N. Haga, N. Manabe, 1998, Clinical dysmorphology.

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

Y. Fukushima, T. Shiihara, S. Ikegawa, 2002, American journal of medical genetics. Part A.