Zobrazeno 1 - 10
of 70
pro vyhledávání: '"FTCDNL1"'
Autor:
Meng, Xu-han1 (AUTHOR), Weng, Yu-ting2 (AUTHOR), Rao, Yu1 (AUTHOR), Xu, Yong-qing1 (AUTHOR), Sun, Hao3 (AUTHOR) sunhao@imbcams.com.cn, Li, Chuan1,4 (AUTHOR) lichuankaka@163.com
Publikováno v:
Journal of Orthopaedic Surgery & Research. 7/1/2024, Vol. 19, p1-8. 8p.
Publikováno v:
Journal of Orthopaedic Surgery and Research, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background Developmental dysplasia of the hip (DDH) is a common cause of childhood disability, and the incidence of DDH shows significant familial aggregation. As the genetic factors of DDH remain unknown, the correlation between five candid
Externí odkaz:
https://doaj.org/article/af54b94db30043b5a65c7adbb4ea12dd
Autor:
Lu, Hsing-Fang1,2, Hung, Kuo-Sheng3,4, Hsu, Yu-Wen1, Tai, Yu-Ting5, Huang, Lin-Shan1, Wang, Yu-Jia1, Wong, Henry Sung-Ching4, Hsu, Yi-Hsiang6,7, Chang, Wei-Chiao1,4 wcc@tmu.edu.tw
Publikováno v:
PLoS ONE. 10/22/2015, Vol. 10 Issue 10, p1-10. 10p.
Autor:
Hsing-Fang Lu, Kuo-Sheng Hung, Yu-Wen Hsu, Yu-Ting Tai, Lin-Shan Huang, Yu-Jia Wang, Henry Sung-Ching Wong, Yi-Hsiang Hsu, Wei-Chiao Chang
Publikováno v:
PLoS ONE, Vol 10, Iss 10, p e0140549 (2015)
Osteoporosis is a systemic skeletal disease characterized by a decreased bone mineral density that results in an increased risk of fragility fractures. Previous studies indicated that genetic factors are involved in the pathogenesis of osteoporosis.
Externí odkaz:
https://doaj.org/article/315465efd68f402690847f6de2f3b611
Autor:
Yu-Ting Tai, Yi-Hsiang Hsu, Hsing Fang Lu, Lin Shan Huang, Wei Chiao Chang, Yu Jia Wang, Kuo Sheng Hung, Henry Sung Ching Wong, Yu Wen Hsu
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 10, p e0140549 (2015)
PLoS ONE, Vol 10, Iss 10, p e0140549 (2015)
Osteoporosis is a systemic skeletal disease characterized by a decreased bone mineral density that results in an increased risk of fragility fractures. Previous studies indicated that genetic factors are involved in the pathogenesis of osteoporosis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de0dbe2a527c0a349b9d7561caa51f8f
http://europepmc.org/articles/PMC4619591
http://europepmc.org/articles/PMC4619591
Genome‐wide Association Study of Methotrexate‐Induced Liver Injury in Rheumatoid Arthritis Patients.
Autor:
Eektimmerman, Frank, Swen, Jesse J., den Broeder, Alfons A., Hazes, Johanna M. W., Kurreeman, Fina S., Verstappen, Suzanne M. M., Nair, Nisha, Pawlik, Andrzej, Nurmohamed, Mike T., Dolžan, Vita, Böhringer, Stefan, Allaart, Cornelia F., Guchelaar, Henk‐Jan
Publikováno v:
Clinical Pharmacology & Therapeutics; Apr2023, Vol. 113 Issue 4, p916-923, 8p
Autor:
Chen, Yu1,2 (AUTHOR), Liu, Sihan1,3 (AUTHOR), Ren, Zongyao1 (AUTHOR), Wang, Feiran1 (AUTHOR), Liang, Qiuman1 (AUTHOR), Jiang, Yi1 (AUTHOR), Dai, Rujia4 (AUTHOR), Duan, Fangyuan1 (AUTHOR), Han, Cong1 (AUTHOR), Ning, Zhilin5 (AUTHOR), Xia, Yan6 (AUTHOR), Li, Miao1 (AUTHOR), Yuan, Kai2 (AUTHOR), Qiu, Wenying7 (AUTHOR), Yan, Xiao-Xin8 (AUTHOR), Dai, Jiapei9 (AUTHOR), Kopp, Richard F.4 (AUTHOR), Huang, Jufang8 (AUTHOR), Xu, Shuhua10 (AUTHOR), Tang, Beisha11 (AUTHOR)
Publikováno v:
American Journal of Human Genetics. Nov2024, Vol. 111 Issue 11, p2444-2457. 14p.
Autor:
Belin, Andrea Carmine1 (AUTHOR), Barloese, Mads Christian2,3 (AUTHOR) mads.barloese@regionh.dk
Publikováno v:
Cephalalgia. Oct2023, Vol. 43 Issue 10, p1-11. 11p.
Publikováno v:
China Oncology. Jul2023, Vol. 33 Issue 7, p673-685. 13p.
Publikováno v:
Razi Journal of Medical Sciences. 2023, Vol. 30 Issue 4, p85-94. 10p.