Furuyama J - Search Results

1

Germline p53 mutation at codon 133 in a cancer-prone family.

Saeki Y, Tamura K, Yamamoto Y, Hatada T, Furuyama J, Utsunomiya J. Saeki Y, et al. Among authors: furuyama j. J Mol Med (Berl). 1997 Jan;75(1):50-6. doi: 10.1007/s001090050086. J Mol Med (Berl). 1997. PMID: 9020384

2

Usefulness of K-ras gene mutation at codon 12 in bile for diagnosing biliary strictures.

Ito R, Tamura K, Ashida H, Nishiwaki M, Nishioka A, Yamamoto Y, Furuyama JI, Utsunomiya J. Ito R, et al. Among authors: furuyama ji. Int J Oncol. 1998 May;12(5):1019-23. doi: 10.3892/ijo.12.5.1019. Int J Oncol. 1998. PMID: 9538122

3

Simple, rapid, and accurate determination of deletion mutations by automated DNA sequencing of heteroduplex fragments of the adenomatous polyposis coli (APC) gene generated by PCR amplification.

Tamura K, Yamamoto Y, Saeki Y, Furuyama J, Utsunomiya J. Tamura K, et al. Among authors: furuyama j. Hum Mutat. 1993;2(6):478-84. doi: 10.1002/humu.1380020609. Hum Mutat. 1993. PMID: 8111416

4

Japanese siblings with missense mutation (717Val --> Ile) in amyloid precursor protein of early-onset Alzheimer's disease.

Matsumura Y, Kitamura E, Miyoshi K, Yamamoto Y, Furuyama J, Sugihara T. Matsumura Y, et al. Among authors: furuyama j. Neurology. 1996 Jun;46(6):1721-3. doi: 10.1212/wnl.46.6.1721. Neurology. 1996. PMID: 8649577

5

Molecular and clinical study of familial adenomatous polyposis for genetic testing and management.

Li G, Tamura K, Yamamoto Y, Sashio H, Utsunomiya J, Yamamura T, Shimoyama T, Furuyama J. Li G, et al. Among authors: furuyama j. J Exp Clin Cancer Res. 1999 Dec;18(4):519-29. J Exp Clin Cancer Res. 1999. PMID: 10746979

6

Mechanism of carcinogenesis in familial tumors.

Tamura K, Utsunomiya J, Iwama T, Furuyama J, Takagawa T, Takeda N, Fukuda Y, Matsumoto T, Nishigami T, Kusuhara K, Sagayama K, Nakagawa K, Yamamura T. Tamura K, et al. Among authors: furuyama j. Int J Clin Oncol. 2004 Aug;9(4):232-45. doi: 10.1007/s10147-004-0430-4. Int J Clin Oncol. 2004. PMID: 15375699 Review.

7

IL18 polymorphism is associated with an increased risk of Crohn's disease.

Tamura K, Fukuda Y, Sashio H, Takeda N, Bamba H, Kosaka T, Fukui S, Sawada K, Tamura K, Satomi M, Yamada T, Yamamura T, Yamamoto Y, Furuyama J, Okamura H, Shimoyama T. Tamura K, et al. Among authors: furuyama j. J Gastroenterol. 2002 Nov;37 Suppl 14:111-6. doi: 10.1007/BF03326428. J Gastroenterol. 2002. PMID: 12572878

8

[Recent trends in studies on carcinogenesis in familial adenomatous polyposis].

Utsunomiya J, Miki Y, Kuroki T, Furuyama J. Utsunomiya J, et al. Among authors: furuyama j. Gan To Kagaku Ryoho. 1988 Feb;15(2):185-91. Gan To Kagaku Ryoho. 1988. PMID: 2829745 Review. Japanese.

9

Are human herpes viruses or measles virus associated with esophageal achalasia?

Niwamoto H, Okamoto E, Fujimoto J, Takeuchi M, Furuyama J, Yamamoto Y. Niwamoto H, et al. Among authors: furuyama j. Dig Dis Sci. 1995 Apr;40(4):859-64. doi: 10.1007/BF02064992. Dig Dis Sci. 1995. PMID: 7720482

10

Polymorphisms of the TNF gene and the TNF receptor superfamily member 1B gene are associated with susceptibility to ulcerative colitis and Crohn's disease, respectively.

Sashio H, Tamura K, Ito R, Yamamoto Y, Bamba H, Kosaka T, Fukui S, Sawada K, Fukuda Y, Tamura K, Satomi M, Shimoyama T, Furuyama J. Sashio H, et al. Among authors: furuyama j. Immunogenetics. 2002 Mar;53(12):1020-7. doi: 10.1007/s00251-001-0423-7. Epub 2002 Feb 7. Immunogenetics. 2002. PMID: 11904678

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