Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Yuumi Ashihara"'
Autor:
Mitsue Saito, Mizuho Kita, Masami Arai, Eri Nakashima, Rie Horii, Reiko Yoshida, Satoko Shimada, Futoshi Akiyama, Shinji Ohno, Dai Kitagawa, Yuumi Ashihara, Sayoko Takeuchi, Naoya Gomi
Publikováno v:
Breast Cancer (Tokyo, Japan)
Individuals carrying pathogenic BRCA1 or BRCA2 mutations have an increased lifetime risk of breast and/or ovarian cancer. The incidence of breast cancer amongst disease-free BRCA mutation carriers under surveillance and the clinical and pathological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2d60b93408569b618e7cdc6767239c7
https://doi.org/10.1007/s12282-019-00971-6
https://doi.org/10.1007/s12282-019-00971-6
Autor:
Yoshio Miki, Yuri Sato, Sachio Nomura, Eri Nakashima, Shinji Ohno, Masami Arai, Reiko Yoshida, Mizuho Kita, Takuji Iwase, Yasue Adachi, Yuumi Ashihara, Dai Kitagawa, Katsutoshi Sato, Mio Koyasu
Publikováno v:
Cancer Science. 108:2287-2294
In addition to BRCA1 and BRCA2, RAD51C, PALB2 and BRIP1 are known as breast cancer susceptibility genes. However, the mutation status of these genes in Japanese familial breast cancer cases has not yet been evaluated. To this end, we analyzed the exo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3bef46b755b36ca4407250508a32505
https://doi.org/10.1111/cas.13350
https://doi.org/10.1111/cas.13350
Autor:
Keiko Taki, Masami Arai, Sachio Nomura, Kokichi Sugano, Yuri Sato, Ikufumi Tajima, Yuumi Ashihara, Mizuho Kita
Publikováno v:
Familial Cancer. 15:261-265
Germline MUTYH mutations were investigated in 14 Japanese colorectal polyposis patients without germ line adenomatous polyposis coli (APC) gene mutations. Three patients had a heterozygous IVS10-2A>G MUTYH mutation. The onset of MUTYH-associated poly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64fb56c12a7786dce583c9cf818f714b
https://doi.org/10.1007/s10689-015-9857-1
https://doi.org/10.1007/s10689-015-9857-1
Autor:
Yuri Sato, Masahiro Igarashi, Koichiro Sato, Chieko Nemoto, Iruru Maetani, Keiko Taki, Tomoyuki Kitagawa, Akiko Chino, Yasuyoshi Sato, Yuumi Ashihara, Masami Arai, Takashi Sekine, Kiyoto Nasuno
Publikováno v:
Japanese Journal of Clinical Oncology. 44:602-606
Familial adenomatous polyposis is an autosomal dominant hereditary disease characterized by the appearance of hundreds to thousands of colorectal adenomatous polyps; if left untreated, there is nearly a 100% lifetime risk of colorectal cancer. In the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13d23546483c08c702b9fefc100e7369
https://doi.org/10.1093/jjco/hyu050
https://doi.org/10.1093/jjco/hyu050
Publikováno v:
Japanese journal of clinical oncology. 46(3)
Objective This study investigated the psychosocial aspects of risk-reducing salpingo-oophorectomy in Japan. Methods The subjects were 16 patients who underwent risk-reducing salpingo-oophorectomy at the Cancer Institute Hospital. Worry about cancer,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ec9b5182ac4c3ffa7953aba0d40df09
https://pubmed.ncbi.nlm.nih.gov/26685323
https://pubmed.ncbi.nlm.nih.gov/26685323
Autor:
Noriko Yamamoto, Yoshiya Fujimoto, Yuri Sato, Junya Yamaguchi, Mizuho Kita, Sachio Nomura, Yuichi Ishikawa, Masashi Ueno, Masami Arai, Yuumi Ashihara
Publikováno v:
Japanese journal of clinical oncology. 45(10)
Heterozygous deleterious mutation of the PMS2 gene is a cause of Lynch syndrome, an autosomal dominant cancer disease. However, the frequency of PMS2 mutation is rare compared with that of the other causative genes; MSH2, MLH1 and MSH6. PMS2 mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85701273c24d704fdf4527bd918dbac3
https://pubmed.ncbi.nlm.nih.gov/26232782
https://pubmed.ncbi.nlm.nih.gov/26232782
Autor:
Masashi Ueno, Noriko Yamamoto, Masahiro Igarashi, Masami Arai, Yuichi Ishikawa, Akiko Chino, Mizuho Kita, Yuri Sato, Ai Sakata, Junya Yamaguchi, Yuumi Ashihara, Satoshi Nagayama, Sachio Nomura
Publikováno v:
Japanese journal of clinical oncology. 44(10)
Juvenile polyposis syndrome is an autosomal dominant inherited disorder characterized by multiple juvenile polyps arising in the gastrointestinal tract and an increased risk of gastrointestinal cancers, specifically colon cancer. BMPR1A and SMAD4 ger
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b6b08e64de29e48ef1842b64f765354
https://pubmed.ncbi.nlm.nih.gov/25129392
https://pubmed.ncbi.nlm.nih.gov/25129392
Publikováno v:
Japanese Journal of Clinical Oncology; Mar2016, Vol. 46 Issue 3, p254-259, 6p
Autor:
Sachio Nomura, Yoshiya Fujimoto, Noriko Yamamoto, Yuri Sato, Yuumi Ashihara, Mizuho Kita, Junya Yamaguchi, Yuichi Ishikawa, Masashi Ueno, Masami Arai
Publikováno v:
Japanese Journal of Clinical Oncology; Oct2015, Vol. 45 Issue 10, p987-992, 6p