Nakamura K - Search Results

1

Mutations in the N-terminal globular domain of the type X collagen gene (COL10A1) in patients with Schmid metaphyseal chondrodysplasia.

Ikegawa S, Nakamura K, Nagano A, Haga N, Nakamura Y. Ikegawa S, et al. Among authors: nakamura y, nakamura k. Hum Mutat. 1997;9(2):131-5. doi: 10.1002/(SICI)1098-1004(1997)9:2<131::AID-HUMU5>3.0.CO;2-C. Hum Mutat. 1997. PMID: 9067753

2

Association of the human NPPS gene with ossification of the posterior longitudinal ligament of the spine (OPLL).

Nakamura I, Ikegawa S, Okawa A, Okuda S, Koshizuka Y, Kawaguchi H, Nakamura K, Koyama T, Goto S, Toguchida J, Matsushita M, Ochi T, Takaoka K, Nakamura Y. Nakamura I, et al. Among authors: nakamura y, nakamura k. Hum Genet. 1999 Jun;104(6):492-7. doi: 10.1007/s004390050993. Hum Genet. 1999. PMID: 10453738

3

Spondylar dysplasia in type X collagenopathy.

Nishimura G, Manabe N, Kosaki K, Haga N, Ohashi H, Nakamura K, Ikegawa S. Nishimura G, et al. Among authors: nakamura k. Pediatr Radiol. 2001 Feb;31(2):76-80. doi: 10.1007/s002470000394. Pediatr Radiol. 2001. PMID: 11214689

4

Identification of sequence polymorphisms of the COMP (cartilage oligomeric matrix protein) gene and association study in osteoarthrosis of the knee and hip joints.

Mabuchi A, Ikeda T, Fukuda A, Koshizuka Y, Hiraoka H, Miyoshi K, Haga N, Kawaguchi H, Kawakami A, Yamamoto S, Takatori Y, Nakamura K, Ikegawa S. Mabuchi A, et al. Among authors: nakamura k. J Hum Genet. 2001;46(8):456-62. doi: 10.1007/s100380170045. J Hum Genet. 2001. PMID: 11501943

5

Identification of sequence polymorphisms in two sulfation-related genes, PAPSS2 and SLC26A2, and an association analysis with knee osteoarthritis.

Ikeda T, Mabuchi A, Fukuda A, Hiraoka H, Kawakami A, Yamamoto S, Machida H, Takatori Y, Kawaguchi H, Nakamura K, Ikegawa S. Ikeda T, et al. Among authors: nakamura k. J Hum Genet. 2001;46(9):538-43. doi: 10.1007/s100380170036. J Hum Genet. 2001. PMID: 11558903

6

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

Mabuchi A, Haga N, Ikeda T, Manabe N, Ohashi H, Takatori Y, Nakamura K, Ikegawa S. Mabuchi A, et al. Among authors: nakamura k. Am J Med Genet. 2001 Nov 22;104(2):135-9. doi: 10.1002/ajmg.10067. Am J Med Genet. 2001. PMID: 11746044

7

Isolation of novel mouse genes associated with ectopic ossification by differential display method using ttw, a mouse model for ectopic ossification.

Koshizuka Y, Ikegawa S, Sano M, Nakamura K, Nakamura Y. Koshizuka Y, et al. Among authors: nakamura y, nakamura k. Cytogenet Cell Genet. 2001;94(3-4):163-8. doi: 10.1159/000048809. Cytogenet Cell Genet. 2001. PMID: 11856874

8

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

Nakamura K, Haga N, Manabe N, Iizuka T. Nakamura K, et al. Clin Dysmorphol. 1998 Jan;7(1):1-10. Clin Dysmorphol. 1998. PMID: 9546823

9

Stature and severity in multiple epiphyseal dysplasia.

Haga N, Nakamura K, Takikawa K, Manabe N, Ikegawa S, Kimizuka M. Haga N, et al. Among authors: nakamura k. J Pediatr Orthop. 1998 May-Jun;18(3):394-7. J Pediatr Orthop. 1998. PMID: 9600570

10

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

Manabe N, Nakamura K, Ikegawa S, Kimizuka M. Manabe N, et al. Among authors: nakamura k. Eur J Radiol. 1998 Sep;28(2):155-9. doi: 10.1016/s0720-048x(97)00116-2. Eur J Radiol. 1998. PMID: 9788021

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