未登录Germline BARD1 variants predispose to mesothelioma by impairing DNA repair and calcium signaling
Novelli, Flavia; Yoshikawa, Yoshie; Vitto, Veronica Angela Maria; Modesti, Lorenzo; Minaai, Michael; Pastorino, Sandra; Emi, Mitsuru; Kim, Jin-Hee; Kricek, Franz; Bai, Fang; Onuchic, Jose N.; Bononi, Angela; Suarez, Joelle S.; Tanji, Mika; Favaron, Cristina; Zolondick, Alicia A.; Xu, Ronghui; Takanishi, Yasutaka; Wang, Zhanwei; Sakamoto, Greg; Gaudino, Giovanni; Grzymski, Joseph; Grosso, Federica; Schrump, David S.; Pass, Harvey I.; Atanesyan, Lilit; Smout, Jan; Savola, Suvi; Sarin, Kavita Y.; Abolhassani, Hassan; Hammarstrom, Lennart; Pan-Hammarstrom, Qiang; Giorgi, Carlotta; Pinton, Paolo; Yang, Haining; Carbone, Michele .png)
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收藏HMGB1 released by mesothelial cells drives the development of asbestos- induced mesotheliomaSuarez, Joelle S.; Novelli, Flavia; Goto, Keisuke; Ehara, Michiko; Steele, Mika; Kim, Jin-Hee; Zolondick, Alicia A.; Xue, Jiaming; Xu, Ronghui; Saito, Mai; Pastorino, Sandra; Minaai, Michael; Takanishi, Yasutaka; Emi, Mitsuru; Pagano, Ian; Wakeham, Andrew; Berger, Thorsten; Pass, Harvey I.; Gaudino, Giovanni; Mak, Tak W.; Carbone, Michele; Yang, Haining 分享 收藏 Heterozygous germline BLM mutations increase susceptibility to asbestos and mesotheliomaBononi, Angela; Goto, Keisuke; Ak, Guntulu; Yoshikawa, Yoshie; Emi, Mitsuru; Pastorino, Sandra; Carparelli, Lorenzo; Ferro, Angelica; Nasu, Masaki; Kim, Jin-Hee; Suarez, Joelle S.; Xu, Ronghui; Tanji, Mika; Takinishi, Yasutaka; Minaai, Michael; Novelli, Flavia; Pagano, Ian; Gaudino, Giovanni; Pass, Harvey, I; Groden, Joanna; Grzymski, Joseph J.; Metintas, Muzaffer; Akarsu, Muhittin; Morrow, Betsy; Hassan, Raffit; Yang, Haining; Carbone, Michele 分享 收藏 分享 收藏 High-density array-CGH with targeted NGS unmask multiple non-contiguous minute deletions on chromosome 3p21 in mesotheliomaCarbone, Michele; Yoshikawa, Yoshie; Emi, Mitsuru; Hashimoto-Tamaoki, Tomoko; Ohmuraya, Masaki; Sato, Ayuko; Tsujimura, Tohru; Hasegawa, Seiki; Nakano, Takashi; Nasu, Masaki; Pastorino, Sandra; Szymiczek, Agata; Bononi, Angela; Pass, Harvey I.; Yang, Haining 分享 收藏 High-density array-CGH with targeted NGS unmask multiple noncontiguous minute deletions on chromosome 3p21 in mesotheliomaYoshikawa, Yoshie; Emi, Mitsuru; Hashimoto-Tamaoki, Tomoko; Ohmuraya, Masaki; Sato, Ayuko; Tsujimura, Tohru; Hasegawa, Seiki; Nakano, Takashi; Nasu, Masaki; Pastorino, Sandra; Szymiczek, Agata; Bononi, Angela; Tanji, Mika; Pagano, Ian; Gaudino, Giovanni; Napolitano, Andrea; Goparaju, Chandra; Pass, Harvey I.; Yang, Haining; Carbone, Michele 分享 收藏 Combined genetic and genealogic studies uncover a large BAP1 cancer syndrome kindred, tracing back nine generations to a common ancestor from the 1700sCarbone, Michele; Flores, Erin G.; Emi, Mitsuru; Gaudino, Giovanni; Pastorino, Sandra; Yang, Haining; Johnson, Todd; Tsunoda, Tatsuhiko; Hesdorffer, Mary; Pass, Harvey I. 分享 收藏 Combined Genetic and Genealogic Studies Uncover a Large BAP1 Cancer Syndrome Kindred Tracing Back Nine Generations to a Common Ancestor from the 1700sCarbone, Michele; Flores, Erin G.; Emi, Mitsuru; Johnson, Todd A.; Tsunoda, Tatsuhiko; Behner, Dusty; Hoffman, Harriet; Hesdorffer, Mary; Nasu, Masaki; Napolitano, Andrea; Powers, Amy; Minaai, Michael; Baumann, Francine; Bryant-Greenwood, Peter; Lauk, Olivia; Kirschner, Michaela B.; Weder, Walter; Opitz, Isabelle; Pass, Harvey I.; Gaudino, Giovanni; Pastorino, Sandra; Yang, Haining 分享 收藏 A founder mutation in the BAP1 gene among four caucasian families with high incidences of malignant peritoneal mesothelioma and uveal melanoma: a molecular and genealogical study in a 10-generation BAP1 cancer syndrome kindredFlores, Erin; Emi, Mitsuru; Johnson, Todd; Tsunoda, Tatsuhiko; Behner, Dusty; Hoffman, Harriet; Hesdorffer, Mary; Nasu, Masaki; Napolitano, Andrea; Baumann, Francine; Yang, Haining; Carbone, Michele 分享 收藏 High incidence of somatic BAP1 alterations in sporadic malignant mesotheliomaNasu, Masaki; Pastorino, Sandra; Luk, Hugh; Flores, Erin; Baumann, Francine; Powers, Amy; Kanodia, Shreya; Gaudino, Giovanni; Zhang, Yu-an; Gazdar, Adi; Yang, Haining; Pass, Harvey I.; Emi, Mitsuru; Carbone, Michele 分享 收藏 Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocationSakazume, Satoru; Ohashi, Hirofumi; Sasaki, Yuki; Harada, Naoki; Nakanishi, Katsumi; Sato, Hidenori; Emi, Mitsuru; Endoh, Kazushi; Sohma, Ryoichi; Kido, Yasuhiro; Nagai, Toshiro; Kubota, Takeo 分享 收藏 分享 收藏 Association of multiple nucleotide variations in the pituitary glutaminyl cyclase gene (QPCT) with low radial BMD in adult womenEzura, Y; Kajita, M; Ishida, R; Yoshida, S; Yoshida, H; Suzuki, T; Hosoi, T; Inoue, S; Shiraki, M; Orimo, H; Emi, M 分享 收藏 Association of a haplotype (196Phe/532Ser) in the interleukin-1-receptor-associated kinase (IRAK1) gene with low radial bone mineral density in two independent populationsIshida, R; Emi, M; Ezura, Y; Iwasaki, H; Yoshida, H; Suzuki, T; Hosoi, T; Inoue, S; Shiraki, M; Ito, H; Orimo, H 分享 收藏 Association of molecular variants, haplotypes, and linkage disequilibrium within the human vitamin D-binding protein (DBP) gene with postmenopausal bone mineral densityEzura, Y; Nakajima, T; Kajita, M; Ishida, R; Inoue, S; Yoshida, H; Suzuki, T; Shiraki, M; Hosoi, T; Orimo, H; Emi, M 分享 收藏 Genetic polymorphisms of paraoxonase-1 are associated with chronic kidney disease in Japanese womenIchikawa, Kazunobu; Konta, Tsuneo; Emi, Mitsuru; Toriyama, Sayumi; Takasaki, Satoshi; Ikeda, Ami; Shibata, Yoko; Takabatake, Noriaki; Takeishi, Yasuchika; Kato, Takeo; Kawata, Sumio; Kubota, Isao 分享 收藏 Common null variant, Arg192Stop, in a G-protein coupled receptor, olfactory receptor 1B1, associated with decreased serum cholinesterase activityKoyano, Satoru; Emi, Mitsuru; Saito, Takafumi; Makino, Naohiko; Toriyama, Sayumi; Ishii, Miho; Kubota, Isao; Kato, Takeo; Kawata, Sumio 分享 收藏 Genetic association between aldehyde dehydrogenase 2 (ALDH2) variation and high-density lipoprotein cholesterol (HDL-C) among non-drinkers in two large population samples in Japan在日本的两个大样本中，非饮酒者中乙醛脱氢酶2 (ALDH2) 变异与高密度脂蛋白胆固醇 (hdl-c) 之间的遗传关联Wada, Manabu; Daimon, Makoto; Emi, Mitsuru; Iijima, Hiroshi; Sato, Hidenori; Koyano, Satoru; Tajima, Katsushi; Kawanami, Toru; Kurita, Keiji; Hunt, Steven C.; Hopkins, Paul N.; Kubota, Isao; Kawata, Sumio; Kato, Takeo 分享 收藏 Association of a single-nucleotide variation (A1330V) in the low-density lipoprotein receptor-related protein 5 gene (LRP5) with bone mineral density in adult Japanese womenEzura, Yoichi; Nakajima, Toshiaki; Urano, Tomohiko; Sudo, Yoshihiro; Kajita, Mitsuko; Yoshida, Hideyo; Suzuki, Takao; Hosoi, Takayuki; Inoue, Satoshi; Shiraki, Masataka; Emi, Mitsuru 分享 收藏 
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