Ikegawa S - Search Results

1

Association study of COL9A2 with lumbar disc disease in the Japanese population.

Seki S, Kawaguchi Y, Mori M, Mio F, Chiba K, Mikami Y, Tsunoda T, Kubo T, Toyama Y, Kimura T, Ikegawa S. Seki S, et al. Among authors: ikegawa s. J Hum Genet. 2006;51(12):1063-1067. doi: 10.1007/s10038-006-0062-9. Epub 2006 Sep 23. J Hum Genet. 2006. PMID: 17024315

2

Mutations of the fibroblast growth factor receptor-3 gene in one familial and six sporadic cases of achondroplasia in Japanese patients.

Ikegawa S, Fukushima Y, Isomura M, Takada F, Nakamura Y. Ikegawa S, et al. Hum Genet. 1995 Sep;96(3):309-11. doi: 10.1007/BF00210413. Hum Genet. 1995. PMID: 7649548

3

Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium.

Toda T, Ikegawa S, Okui K, Kondo E, Saito K, Fukuyama Y, Yoshioka M, Kumagai T, Suzumori K, Kanazawa I, et al. Toda T, et al. Among authors: ikegawa s. Am J Hum Genet. 1994 Nov;55(5):946-50. Am J Hum Genet. 1994. PMID: 7977357 Free PMC article.

4

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. 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

5

Mutation of the type X collagen gene (COL10A1) causes spondylometaphyseal dysplasia.

Ikegawa S, Nishimura G, Nagai T, Hasegawa T, Ohashi H, Nakamura Y. Ikegawa S, et al. Am J Hum Genet. 1998 Dec;63(6):1659-62. doi: 10.1086/302158. Am J Hum Genet. 1998. PMID: 9837818 Free PMC article.

6

Novel and recurrent COMP (cartilage oligomeric matrix protein) mutations in pseudoachondroplasia and multiple epiphyseal dysplasia.

Ikegawa S, Ohashi H, Nishimura G, Kim KC, Sannohe A, Kimizuka M, Fukushima Y, Nagai T, Nakamura Y. Ikegawa S, et al. Hum Genet. 1998 Dec;103(6):633-8. doi: 10.1007/s004390050883. Hum Genet. 1998. PMID: 9921895

7

Genomic organization, mapping, and polymorphisms of the gene encoding human cartilage intermediate layer protein (CILP).

Nakamura I, Okawa A, Ikegawa S, Takaoka K, Nakamura Y. Nakamura I, et al. Among authors: ikegawa s. J Hum Genet. 1999;44(3):203-5. doi: 10.1007/s100380050143. J Hum Genet. 1999. PMID: 10319588

8

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: ikegawa s. Hum Genet. 1999 Jun;104(6):492-7. doi: 10.1007/s004390050993. Hum Genet. 1999. PMID: 10453738

9

Novel and recurrent EBP mutations in X-linked dominant chondrodysplasia punctata.

Ikegawa S, Ohashi H, Ogata T, Honda A, Tsukahara M, Kubo T, Kimizuka M, Shimode M, Hasegawa T, Nishimura G, Nakamura Y. Ikegawa S, et al. Am J Med Genet. 2000 Oct 2;94(4):300-5. doi: 10.1002/1096-8628(20001002)94:4<300::aid-ajmg7>3.0.co;2-3. Am J Med Genet. 2000. PMID: 11038443 Review.

10

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: ikegawa s. J Hum Genet. 2001;46(8):456-62. doi: 10.1007/s100380170045. J Hum Genet. 2001. PMID: 11501943

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