Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Mika Okazawa"'
Autor:
Mashu Futagawa, Hideki Yamamoto, Mariko Kochi, Yusaku Urakawa, Reimi Sogawa, Fumino Kato, Mika Okazawa-Sakai, Daisuke Ennishi, Katsunori Shinozaki, Hirofumi Inoue, Hiroyuki Yanai, Akira Hirasawa
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 19, Iss 1, Pp 1-7 (2021)
Abstract Background RAD51D (RAD51 paralog D) is an intermediate cancer susceptibility gene for primary ovarian cancer, including fallopian tube and peritoneal carcinomas and breast cancer. Although gynecological non-epithelial tumors such as uterine
Externí odkaz:
https://doaj.org/article/44be1e99494e4db990fec38e106ce428
Autor:
Takanori Yokoyama, Kazuhiro Takehara, Nao Sugimoto, Keika Kaneko, Etsuko Fujimoto, Mika Okazawa-Sakai, Shinichi Okame, Yuko Shiroyama, Takashi Yokoyama, Norihiro Teramoto, Shozo Ohsumi, Shinya Saito, Kazuho Imai, Kokichi Sugano
Publikováno v:
BMC Cancer, Vol 18, Iss 1, Pp 1-4 (2018)
Abstract Background Lynch syndrome is an autosomal dominant inherited disease caused by germline mutations in mismatch repair genes. Analysis for microsatellite instability (MSI) and immunohistochemistry (IHC) of protein expressions of disease-associ
Externí odkaz:
https://doaj.org/article/4e7d93dc0a284bdfbaa966cb92a5402a
Autor:
Mika, Okazawa-Sakai, Yasuko, Yamamoto, Mashu, Futagawa, Miki, Okamura, Satoko, Miyawaki, Tomohiro, Nishina, Kazuhiro, Takehara, Toshiyuki, Kozuki, Shuta, Tomida, Ichinosuke, Hyodo, Shozo, Ohsumi, Akira, Hirasawa
Publikováno v:
Acta Medica Okayama. 76(6):673-678
Patients found to have presumed germline pathogenic variants (PGPVs) during comprehensive genomic profiling (CGP) require genetic counseling (GC) referrals. We retrospectively investigated the outcomes of patients with PGPVs. Among 159 patients who u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1aee6374146e61685351422c18e46cc9
https://ousar.lib.okayama-u.ac.jp/64117
https://ousar.lib.okayama-u.ac.jp/64117
Autor:
Tamaki Tanaka, Kazuhiro Takehara, Natsumi Yamashita, Mika Okazawa-Sakai, Kazuya Kuraoka, Norihiro Teramoto, Kenichi Taguchi, Katsushige Yamashiro, Hidenori Kato, Tomoya Mizunoe, Rie Suzuki, Dan Yamamoto, Arisa Ueki, Toshiaki Saito
Publikováno v:
Journal of Gynecologic Oncology. 33
To clarify the frequency of deficient mismatch repair (dMMR) in Japanese ovarian cancer patients, we examined microsatellite instability (MSI) status and immunohistochemistry (IHC) subtypes, including endometrioid carcinoma (EMC), clear cell carcinom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c43d4a501b3d78f6cb13cb392c7dca6
https://doi.org/10.3802/jgo.2022.33.e67
https://doi.org/10.3802/jgo.2022.33.e67
Autor:
Akira Hirasawa, Mika Okazawa-Sakai
Publikováno v:
Hereditary Breast and Ovarian Cancer ISBN: 9789811645204
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::848272e91eb9903ea75fb3dacb17a247
https://doi.org/10.1007/978-981-16-4521-1_14
https://doi.org/10.1007/978-981-16-4521-1_14
Autor:
Etsuko Fujimoto, Norihiro Teramoto, Tamaki Tanaka, Kazuhiro Takehara, Takanori Yokoyama, Katsuyuki Tomono, Shinichi Okame, Mika Okazawa-Sakai, Yoshifumi Sugawara
Publikováno v:
International Cancer Conference Journal. 8:33-38
Uterine leiomyosarcoma is a rare type of malignant gynecological tumor and has a poor prognosis; therefore, this tumor is often difficult to treat. Some new drugs have been approved during the past several years in Japan and are expected to be effica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fa031cf5a56300d4e7abfd14eff0c17
https://doi.org/10.1007/s13691-018-0350-1
https://doi.org/10.1007/s13691-018-0350-1
Autor:
Shinya Saito, Nao Sugimoto, Norihiro Teramoto, Takashi Yokoyama, Kazuhiro Takehara, Keika Kaneko, Yuko Shiroyama, Takanori Yokoyama, Shinichi Okame, Mika Okazawa-Sakai, Kokichi Sugano, Shozo Ohsumi, Kazuho Imai, Etsuko Fujimoto
Publikováno v:
BMC Cancer, Vol 18, Iss 1, Pp 1-4 (2018)
BMC Cancer
BMC Cancer
Background Lynch syndrome is an autosomal dominant inherited disease caused by germline mutations in mismatch repair genes. Analysis for microsatellite instability (MSI) and immunohistochemistry (IHC) of protein expressions of disease-associated gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e81757056e7d452243fc9fe439526326
http://link.springer.com/article/10.1186/s12885-018-4489-0
http://link.springer.com/article/10.1186/s12885-018-4489-0
Autor:
Hideki Yamamoto, Daisuke Ennishi, Akira Hirasawa, Katsunori Shinozaki, Hirofumi Inoue, Fumino Kato, Mika Okazawa-Sakai, Mariko Kochi, Yusaku Urakawa, Reimi Sogawa, Hiroyuki Yanai, Mashu Futagawa
Publikováno v:
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice, Vol 19, Iss 1, Pp 1-7 (2021)
Hereditary Cancer in Clinical Practice, Vol 19, Iss 1, Pp 1-7 (2021)
Background RAD51D (RAD51 paralog D) is an intermediate cancer susceptibility gene for primary ovarian cancer, including fallopian tube and peritoneal carcinomas and breast cancer. Although gynecological non-epithelial tumors such as uterine sarcomas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fd8857d354e189ffa6f3ec970e57f7b
https://ousar.lib.okayama-u.ac.jp/62989
https://ousar.lib.okayama-u.ac.jp/62989
Autor:
Eriko Yokoi, Tadashi Kimura, Kazuhiko Ogawa, Seiji Mabuchi, Mika Okazawa-Sakai, A. Kawashima, Fumiaki Isohashi
Publikováno v:
Journal of Obstetrics and Gynaecology Research. 43:1743-1750
Aim To investigate the predictors of distant relapse in International Federation of Gynecology and Obstetrics (FIGO) stage IIB-IVA cervical cancer patients treated with definitive radiotherapy (RT). Methods The clinical data of 219 patients with FIGO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c995f46b7724ce7475a42766c1c71e0
https://doi.org/10.1111/jog.13446
https://doi.org/10.1111/jog.13446
Autor:
Gen Yamada, Masayo Harada, Naomi Nakagata, Mika Okazawa, Mitsuru Morimoto, Masafumi Noguchi, Aki Murashima, David M. Ornitz, Tadashi Kimura
Publikováno v:
Developmental biology
The Wolffian duct (WD) is a primordium of the male reproductive tract and kidney collecting duct system. Fibroblast growth factor receptors (FGFRs), members of the receptor tyrosine kinase (RTK) family, are essential for kidney development. Although
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b66bbd0989aac96e88e4a6883e5e044
https://doi.org/10.1016/j.ydbio.2015.01.023
https://doi.org/10.1016/j.ydbio.2015.01.023