Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: ANXA3[original query] |
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Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese.
PloS one 2012 7 (4): e32683. Osman Wael, Okada Yukinori, Kamatani Yoichiro, Kubo Michiaki, Matsuda Koichi, Nakamura Yusu |
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population.
Nature genetics 2012 May 44 (5): 511-6. Okada Yukinori, Terao Chikashi, Ikari Katsunori, Kochi Yuta, Ohmura Koichiro, Suzuki Akari, Kawaguchi Takahisa, Stahl Eli A, Kurreeman Fina A S, Nishida Nao, Ohmiya Hiroko, Myouzen Keiko, Takahashi Meiko, Sawada Tetsuji, Nishioka Yuichi, Yukioka Masao, Matsubara Tsukasa, Wakitani Shigeyuki, Teshima Ryota, Tohma Shigeto, Takasugi Kiyoshi, Shimada Kota, Murasawa Akira, Honjo Shigeru, Matsuo Keitaro, Tanaka Hideo, Tajima Kazuo, Suzuki Taku, Iwamoto Takuji, Kawamura Yoshiya, Tanii Hisashi, Okazaki Yuji, Sasaki Tsukasa, Gregersen Peter K, Padyukov Leonid, Worthington Jane, Siminovitch Katherine A, Lathrop Mark, Taniguchi Atsuo, Takahashi Atsushi, Tokunaga Katsushi, Kubo Michiaki, Nakamura Yusuke, Kamatani Naoyuki, Mimori Tsuneyo, Plenge Robert M, Yamanaka Hisashi, Momohara Shigeki, Yamada Ryo, Matsuda Fumihiko, Yamamoto Kazuhi |
PADI4 and HLA-DRB1 are genetic risks for radiographic progression in RA patients, independent of ACPA status: results from the IORRA cohort study. PloS one 2013 8 (4): e61045. Suzuki Taku, Ikari Katsunori, Yano Koichiro, Inoue Eisuke, Toyama Yoshiaki, Taniguchi Atsuo, Yamanaka Hisashi, Momohara Shige |
Huntington's disease biomarker progression profile identified by transcriptome sequencing in peripheral blood. European journal of human genetics : EJHG 2015 Oct 23 (10): 1349-56. Mastrokolias Anastasios, Ariyurek Yavuz, Goeman Jelle J, van Duijn Erik, Roos Raymund Ac, van der Mast Roos C, van Ommen GertJan B, den Dunnen Johan T, 't Hoen Peter Ac, van Roon-Mom Willeke |
Whole genome sequencing identifies ANXA3 and MTHFR mutations in a large family with an unknown equinus deformity associated genetic disorder. Molecular biology reports 2016 Jul . Zhang Zhiqun, Kong Zhuqing, Zhu Miao, Lu Wenxiang, Ni Lei, Bai Yunfei, Lou Y |
Microarray-based SNP genotyping to identify genetic risk factors of triple-negative breast cancer (TNBC) in South Indian population. Molecular and cellular biochemistry 2017 Sep . Aravind Kumar M, Singh Vineeta, Naushad Shaik Mohammad, Shanker Uday, Lakshmi Narasu |
Germline Mutations in Familial Papillary Thyroid Cancer. Endocrine pathology 2020 Feb . Sarquis Marta, Moraes Debora C, Bastos-Rodrigues Luciana, Azevedo Pedro G, Ramos Adauto V, Reis Fabiana Versiani, Dande Paula V, Paim Isabela, Friedman Eitan, De Marco Lu |
Identification of Up-Regulated ANXA3 Resulting in Fracture Non-Union in Patients With T2DM. Frontiers in endocrinology 2022 13 890941. Liu Changjiang, Liu Yuhang, Yu Yifeng, Zhao Yong, Zhang Dong, Yu Ai |
Genetic Influence of Fracture Nonunion (FNU): A Systematic Review. Pharmacogenomics and personalized medicine 2023 6 16 569-575. Mir Sadat-Ali, Hussain K Al-Omar, Khalid W AlTabash, Ammar K AlOmran, Dakheel A AlDakheel, Hasan N AlSay |
Evaluation of a gene signature related to thrombotic manifestations in antiphospholipid syndrome. Frontiers in medicine 2023 4 10 1139906. Jacintho Bruna Cardoso, Mazetto Fonseca Bruna de Moraes, Hounkpe Bidossessi Wilfried, Oliveira Jose Diogo, Dos Santos Ana Paula Rosa, Vaz Camila de Oliveira, de Paula Erich Vinicius, Orsi Fernanda Andra |
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- Page last updated:Apr 22, 2024
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