Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Noriko Fukayama"'
Autor:
Mariko Taylor, Satoshi Ozawa, Tsuyoshi Sonehara, Akira Ichikawa, Yuji Miyahara, Takashi Irie, Noriko Fukayama, Kokichi Sugano, Shinichi Fukuzono
Publikováno v:
Analytical Chemistry. 76:6122-6129
Since the successful completion of the Human Genome Project, increasing concern is being directed toward the polymorphic aspect of the genome and its clinical relevance. A form of single-strand DNA-conformation polymorphism analysis (SSCP) employing
Autor:
Hideki Ishikawa, Naohiro Tomita, Tomohiko Aihara, Shigeyuki Tamura, Keishi Sugimoto, Nariaki Matsuura, Hiroki Ohzato, Ken Nakata, Hirofumi Miki, Mutsumi Fukunaga, Kokichi Sugano, Takeshi Iwanaga, Shu Okamura, Noriko Fukayama, Yuuichi Takatsuka
Publikováno v:
Japanese Journal of Clinical Oncology. 34:556-560
Hereditary non-polyposis colorectal cancer (HNPCC) is a very important clinical entity in oncology. In order to identify HNPCC, the international diagnostic criteria, named 'Amsterdam criteria', has been used. In this report, we present a patient wit
Autor:
Tomohiko Aihara, Naohiro Tomita, Keishi Sugimoto, Yuuichi Takatsuka, Kokichi Sugano, Hiroki Ohzato, Noriko Fukayama, Nariaki Matsuura, Takeshi Iwanaga, Shigeyuki Tamura, Hirofumi Miki, Mutsumi Fukunaga
Publikováno v:
Japanese Journal of Clinical Oncology. 33:486-489
Hereditary non-polyposis colorectal cancer (HNPCC) is a very important clinical entity in oncology. In order to identify HNPCC, the international diagnostic criteria named "Amsterdam criteria" have been used. In this report, we present a case of an H
The Novel Germline Mutation of hMSH2 Gene in a Case of a Colon Cancer Patient Without Family History
Autor:
Kokichi Sugano, Norikazu Masuda, Naohiro Tomita, Takashi Satomi, Hiroshi Imamura, Hiroshi Furukawa, Junzo Shimizu, Takatoshi Kawasaki, Noriko Fukayama, Masayuki Tatsuta, Hideyuki Ishida, Seizo Masutani
Publikováno v:
Japanese Journal of Clinical Oncology. 32:266-269
Hereditary non-polyposis colorectal cancer (HNPCC) is generally found from the patient's family history. The functional disorder of mismatch repair genes has been reported to be responsible for HNPCC. The proband was a 28-year-old Japanese female who
Autor:
Kokichi Sugano, Noriko Fukayama, Hidefumi Kashiwabara, Sachio Nomura, Shin Fujita, Takao Sekiya, Takahiro Taniguchi, Tadao Kakizoe, Seiji Ohhigashi, Takayuki Akasu, Yoshihiro Moriya
Publikováno v:
Biochemical and Biophysical Research Communications. 271:120-129
Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal, dominantly inherited cancer-prone syndrome. Here, we describe a novel and efficient approach for screening mutations of two major HNPCC susceptibility genes, hMSH2 and hMLH1. The syst
Autor:
Masashi Niwakawa, Takao Sekiya, Kayako Shimamura, Noriko Fukayama, Hiroyuki Fujimoto, Takahiro Taniguchi, Naoto Doi, Tadao Kakizoe, Ken-ichi Tobisu, Taiji Tsukamoto, Kokichi Sugano, Masanori Shigyo
Publikováno v:
International Journal of Cancer. 78:425-429
Allelic loss on chromosome 9 is the most frequent and earliest genetic event in bladder carcinogenesis, and its detection in urine samples would be useful for detecting bladder cancer. A highly sensitive method to detect loss of heterozygosity (LOH)
Autor:
Toshihiro Yokota, Noriko Fukayama, Shigeaki Yoshida, Atsushi Ochiai, Kenichi Sugihara, Daizo Saito, Kokichi Sugano, Hisanao Ohkura, Hitoshi Kondo
Publikováno v:
Gastrointestinal Endoscopy. 46:61-65
Aberrant crypt foci (ACF), first described by Bird et al., 1 have been considered an early event in colorectal carcinogenesis because they are associated with a carcinogen-induced model of colorectal tumorigenesis in rodents TM and are present at a g
Autor:
Atsushi Ohtsu, Kokichi Sugano, Hitoshi Kondo, Koichi Hosokawa, Hisanao Ohkura, Kiyoshi Mukai, Shigeaki Yoshida, Noriko Fukayama
Publikováno v:
Cancer. 79:900-905
BACKGROUND The authors previously found specific mutations of the K-ras gene at codon 12 in the pancreatic juice of 67% of patients (6 of 9) with pancreatic ductal carcinoma, and the detection of these mutations was useful for diagnosis. This study w
Autor:
Noriko Fukayama, Masato Maekawa, Yuki Nakashima, Hisanao Ohkura, Kokichi Sugano, Takao Sekiya, Kensei Yamaguchi, Tadao Kakizoe
Publikováno v:
Genes, Chromosomes and Cancer. 15:157-164
We have developed a fluorescence-based single-strand conformation polymorphism analysis to detect HaeIII-sensitive polymorphic sites in intron I of the TP53 gene. It is important to treat the PCR products with Klenow fragment to remove a 3′-protrud
Autor:
Kazuaki Shimada, Hitoshi Kondo, Shigeaki Yoshida, Noriko Fukayama, Hisanao Ohkura, Akiko Kyogoku, Haruhiko Nose, Atsushi Ohtsu, Yukio Shimosato, Kokichi Sugano
Publikováno v:
Cancer. 73:1589-1594
Background. Mutations in the K-ras oncogene at codon 12 are detected at a remarkably high frequency in pancreatic carcinomas and are believed to be a critical event in oncogenesis. The authors attempted to detect K-ras mutations in DNA obtained from