Human Genome Epidemiology Literature Finder
|
Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and PRKCB[original query] |
|---|
| PRKCB is associated with calcineurin inhibitor-induced renal dysfunction in heart transplant recipients. Pharmacogenetics and genomics 2012 Feb . Lachance K, Barhdadi A, Mongrain I, Normand V, Zakrzewski M, Leblanc MH, Racine N, Carrier M, Ducharme A, Turgeon J, Dubé MP, Phillips MS, White M, de Denus S |
| Identification of microRNAs regulated by isothiocyanates and association of polymorphisms inside their target sites with risk of sporadic colorectal cancer. Nutrition and cancer 2013 65 (2): 247-54. Slaby Ondrej, Sachlova Milana, Brezkova Veronika, Hezova Renata, Kovarikova Alena, Bischofová Svatava, Sevcikova Sabina, Bienertova-Vasku Julie, Vasku Anna, Svoboda Marek, Vyzula Rostisl |
| Prognostic relevance of integrated genetic profiling in adult T-cell leukemia/lymphoma. Blood 2017 Oct . Kataoka Keisuke, Iwanaga Masako, Yasunaga Jun-Ichirou, Nagata Yasunobu, Kitanaka Akira, Kameda Takuro, Yoshimitsu Makoto, Shiraishi Yuichi, Sato-Otsubo Aiko, Sanada Masashi, Chiba Kenichi, Tanaka Hiroko, Ochi Yotaro, Aoki Kosuke, Suzuki Hiromichi, Shiozawa Yusuke, Yoshizato Tetsuichi, Sato Yusuke, Yoshida Kenichi, Nosaka Kisato, Hishizawa Masakatsu, Itonaga Hidehiro, Imaizumi Yoshitaka, Munakata Wataru, Shide Kotaro, Kubuki Yoko, Hidaka Tomonori, Nakamaki Tsuyoshi, Ishiyama Ken, Miyawaki Shuichi, Ishii Ryohei, Nureki Osamu, Tobinai Kensei, Miyazaki Yasushi, Takaori-Kondo Akifumi, Shibata Tatsuhiro, Miyano Satoru, Ishitsuka Kenji, Utsunomiya Atae, Shimoda Kazuya, Matsuoka Masao, Watanabe Toshiki, Ogawa Seis |
Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population.
Human molecular genetics 2017 Jan . Kawashima Minae, Hitomi Yuki, Aiba Yoshihiro, Nishida Nao, Kojima Kaname, Kawai Yosuke, Nakamura Hitomi, Tanaka Atsushi, Zeniya Mikio, Hashimoto Etsuko, Ohira Hiromasa, Yamamoto Kazuhide, Abe Masanori, Nakao Kazuhiko, Yamagiwa Satoshi, Kaneko Shuichi, Honda Masao, Umemura Takeji, Ichida Takafumi, Seike Masataka, Sakisaka Shotaro, Harada Masaru, Yokosuka Osamu, Ueno Yoshiyuki, Senju Michio, Kanda Tatsuo, Shibata Hidetaka, Himoto Takashi, Murata Kazumoto, Miyake Yasuhiro, Ebinuma Hirotoshi, Taniai Makiko, Joshita Satoru, Nikami Toshiki, Ota Hajime, Kouno Hiroshi, Kouno Hirotaka, Nakamuta Makoto, Fukushima Nobuyoshi, Kohjima Motoyuki, Komatsu Tatsuji, Komeda Toshiki, Ohara Yukio, Muro Toyokichi, Yamashita Tsutomu, Yoshizawa Kaname, Nakamura Yoko, Shimada Masaaki, Hirashima Noboru, Sugi Kazuhiro, Ario Keisuke, Takesaki Eiichi, Naganuma Atsushi, Mano Hiroshi, Yamashita Haruhiro, Matsushita Kouki, Yamauchi Kazuhiko, Makita Fujio, Nishimura Hideo, Furuta Kiyoshi, Takahashi Naohiro, Kikuchi Masahiro, Masaki Naohiko, Tanaka Tomohiro, Tamura Sumito, Mori Akira, Yagi Shintaro, Shirabe Ken, Komori Atsumasa, Migita Kiyoshi, Ito Masahiro, Nagaoka Shinya, Abiru Seigo, Yatsuhashi Hiroshi, Yasunami Michio, Shimoda Shinji, Harada Kenichi, Egawa Hiroto, Maehara Yoshihiko, Uemoto Shinji, Kokudo Norihiro, Takikawa Hajime, Ishibashi Hiromi, Chayama Kazuaki, Mizokami Masashi, Nagasaki Masao, Tokunaga Katsushi, Nakamura Mino |
| Increased expression of PRKCB mRNA in peripheral blood mononuclear cells from patients with systemic lupus erythematosus. Annals of human genetics 2018 Jan . Zhu Zhengwei, Yang Lulu, Zhang Yaohua, Liu Lu, Huang Yan, Wen Leilei, Yang Chao, Chen Liyun, Wang Wenjun, Zuo Xianbo, Zhou Fusheng, Wang Hongyan, Tang Huayang, Zhang Xuejun, Yang Sen, Sheng Yujun, Cui Yo |
| Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease. Ear and hearing 2020 11 41 (6): 1598-1605. Roman-Naranjo Pablo, Gallego-Martinez Alvaro, Soto-Varela Andrés, Aran Ismael, Moleon Maria Del Carmen, Espinosa-Sanchez Juan Manuel, Amor-Dorado Juan Carlos, Batuecas-Caletrio Angel, Perez-Vazquez Paz, Lopez-Escamez Jose Anton |
| A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies.
Brain : a journal of neurology 2022 3 . Strippel Christine, Herrera-Rivero Marisol, Wendorff Mareike, Tietz Anja K, Degenhardt Frauke, Witten Anika, Schroeter Christina, Nelke Christopher, Golombeck Kristin S, Madlener Marie, Rüber Theodor, Ernst Leon, Racz Attila, Baumgartner Tobias, Widman Guido, Doppler Kathrin, Thaler Franziska, Siebenbrodt Kai, Dik Andre, Kerin Constanze, Räuber Saskia, Gallus Marco, Kovac Stjepana, Grauer Oliver M, Grimm Alexander, Prüss Harald, Wickel Jonathan, Geis Christian, Lewerenz Jan, Goebels Norbert, Ringelstein Marius, Menge Til, Tackenberg Björn, Kellinghaus Christoph, Bien Christian G, Kraft Andrea, Zettl Uwe, Ismail Fatme Seval, Ayzenberg Ilya, Urbanek Christian, Sühs Kurt-Wolfram, Tauber Simone C, Mues Sigrid, Körtvélyessy Peter, Markewitz Robert, Paliantonis Asterios, Elger Christian E, Surges Rainer, Sommer Claudia, Kümpfel Tania, Gross Catharina C, Lerche Holger, Wellmer Jörg, Quesada Carlos M, Then Bergh Florian, Wandinger Klaus-Peter, Becker Albert J, Kunz Wolfram S, Meyer Zu Hörste Gerd, Malter Michael P, Rosenow Felix, Wiendl Heinz, Kuhlenbäumer Gregor, Leypoldt Frank, Lieb Wolfgang, Franke Andre, Meuth Sven G, Stoll Monika, Melzer Nico, |
| The obesity-related mutation gene on nonalcoholic fatty liver disease. Human genetics 2024 7 . Yen-Yu Chen, Chi-Sheng Chen, Jee-Fu Huang, Wen-Hsiu Su, Chia-Yang Li, Wei-Shiun Chen, En-Sheng Lin, Wan-Long Chuang, Ming-Lung Yu, Shu-Chi Wa |
- Page last reviewed:Feb 1, 2024
- Content source: