Orimo H - Search Results

1

Close correlation between mutations of E2F4 and hMSH3 genes in colorectal cancers with microsatellite instability.

Ikeda M, Orimo H, Moriyama H, Nakajima E, Matsubara N, Mibu R, Tanaka N, Shimada T, Kimura A, Shimizu K. Ikeda M, et al. Among authors: orimo h. Cancer Res. 1998 Feb 15;58(4):594-8. Cancer Res. 1998. PMID: 9485005

2

A novel missense mutation and frameshift mutations in the type II receptor of transforming growth factor-beta gene in sporadic colon cancer with microsatellite instability.

Orimo H, Ikejima M, Nakajima E, Emi M, Shimada T. Orimo H, et al. Mutat Res. 1998 May;382(3-4):115-20. doi: 10.1016/s1383-5726(98)00003-x. Mutat Res. 1998. PMID: 9691992

3

Frameshift mutations and a length polymorphism in the hMSH3 gene and the spectrum of microsatellite instability in sporadic colon cancer.

Orimo H, Nakajima E, Ikejima M, Emi M, Shimada T. Orimo H, et al. Jpn J Cancer Res. 1999 Dec;90(12):1310-5. doi: 10.1111/j.1349-7006.1999.tb00713.x. Jpn J Cancer Res. 1999. PMID: 10665647 Free PMC article.

4

Association between single nucleotide polymorphisms in the hMSH3 gene and sporadic colon cancer with microsatellite instability.

Orimo H, Nakajima E, Yamamoto M, Ikejima M, Emi M, Shimada T. Orimo H, et al. J Hum Genet. 2000;45(4):228-30. doi: 10.1007/s100380070031. J Hum Genet. 2000. PMID: 10944853

5

Nine-bp repeat polymorphism in exon 1 of the hMSH3 gene.

Nakajima E, Orimo H, Ikejima M, Shimada T. Nakajima E, et al. Among authors: orimo h. Jpn J Hum Genet. 1995 Dec;40(4):343-5. doi: 10.1007/BF01900603. Jpn J Hum Genet. 1995. PMID: 8851770

6

Loss of expression of the human MSH3 gene in hematological malignancies.

Inokuchi K, Ikejima M, Watanabe A, Nakajima E, Orimo H, Nomura T, Shimada T. Inokuchi K, et al. Among authors: orimo h. Biochem Biophys Res Commun. 1995 Sep 5;214(1):171-9. doi: 10.1006/bbrc.1995.2271. Biochem Biophys Res Commun. 1995. PMID: 7669036

7

Mutational analysis and functional correlation with phenotype in German patients with childhood-type hypophosphatasia.

Orimo H, Girschick HJ, Goseki-Sone M, Ito M, Oda K, Shimada T. Orimo H, et al. J Bone Miner Res. 2001 Dec;16(12):2313-9. doi: 10.1359/jbmr.2001.16.12.2313. J Bone Miner Res. 2001. PMID: 11760847 Free article.

8

G317D mutation in the tissue-nonspecific alkaline phosphatase gene associated with childhood hypophosphatasia in a German family.

Orimo H, Shin YS, Shimada T. Orimo H, et al. J Inherit Metab Dis. 2002 Nov;25(7):601-2. doi: 10.1023/a:1022055710295. J Inherit Metab Dis. 2002. PMID: 12638946 No abstract available.

9

Expression of the mutant (1735T-DEL) tissue-nonspecific alkaline phosphatase gene from hypophosphatasia patients.

Goseki-Sone M, Orimo H, Iimura T, Miyazaki H, Oda K, Shibata H, Yanagishita M, Takagi Y, Watanabe H, Shimada T, Oida S. Goseki-Sone M, et al. Among authors: orimo h. J Bone Miner Res. 1998 Dec;13(12):1827-34. doi: 10.1359/jbmr.1998.13.12.1827. J Bone Miner Res. 1998. PMID: 9844100 Free article.

10

Expression of bone morphogenetic proteins and rat distal-less homolog genes following rat femoral fracture.

Yaoita H, Orimo H, Shirai Y, Shimada T. Yaoita H, et al. Among authors: orimo h. J Bone Miner Metab. 2000;18(2):63-70. doi: 10.1007/s007740050013. J Bone Miner Metab. 2000. PMID: 10701160

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