Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Syndrome and TNFSF15[original query] |
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| Genetic susceptibility to inflammation and colonic transit in lower functional gastrointestinal disorders: preliminary analysis. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2011 Oct 23 (10): 935-e398. Camilleri M, Carlson P, McKinzie S, Zucchelli M, D'Amato M, Busciglio I, Burton D, Zinsmeister A |
| Association of TNFSF15 polymorphism with irritable bowel syndrome. Gut 2011 Dec 60 (12): 1671-7. Zucchelli Marco, Camilleri Michael, Andreasson Anna Nixon, Bresso Francesca, Dlugosz Aldona, Halfvarson Jonas, Törkvist Leif, Schmidt Peter T, Karling Pontus, Ohlsson Bodil, Duerr Richard H, Simren Magnus, Lindberg Greger, Agreus Lars, Carlson Paula, Zinsmeister Alan R, D'Amato Mau |
| Identifying and testing candidate genetic polymorphisms in the irritable bowel syndrome (IBS): association with TNFSF15 and TNFa. Gut 2013 Jul 62 (7): 985-94. Swan Caroline, Duroudier Nathalie P, Campbell Eugene, Zaitoun Abed, Hastings Margaret, Dukes George E, Cox Joanne, Kelly Fiona M, Wilde Jonathan, Lennon Mark G, Neal Keith R, Whorwell Peter J, Hall Ian P, Spiller Robin |
| Genetic variation in GPBAR1 predisposes to quantitative changes in colonic transit and bile acid excretion. American journal of physiology. Gastrointestinal and liver physiology 2014 Sep 307 (5): G508-16. Camilleri Michael, Shin Andrea, Busciglio Irene, Carlson Paula, Acosta Andres, Bharucha Adil E, Burton Duane, Lamsam Jesse, Lueke Alan, Donato Leslie J, Zinsmeister Alan |
| A meta-analysis of immunogenetic Case-Control Association Studies in irritable bowel syndrome. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2015 May 27 (5): 717-27. Czogalla B, Schmitteckert S, Houghton L A, Sayuk G S, Camilleri M, Olivo-Diaz A, Spiller R, Wouters M M, Boeckxstaens G, Bermejo J Lorenzo, Niesler |
| Associations between TNFSF4, TNFSF8 and TNFSF15 and Behçet's disease but not VKH syndrome in Han Chinese. Oncotarget 2017 Dec 8 (62): 105037-105046. Jiang Yan, Cheng Ling, Li Xin, Zhou Wenke, Zhang |
| Candidate single nucleotide polymorphisms of irritable bowel syndrome: a systemic review and meta-analysis. BMC gastroenterology 2019 Oct 19 (1): 165. Zhu Shiwei, Wang Ben, Jia Qiong, Duan Lipi |
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome.
Kidney international 2020 11 98 (5): 1308-1322. Jia Xiaoyuan, Yamamura Tomohiko, Gbadegesin Rasheed, McNulty Michelle T, Song Kyuyong, Nagano China, Hitomi Yuki, Lee Dongwon, Aiba Yoshihiro, Khor Seik-Soon, Ueno Kazuko, Kawai Yosuke, Nagasaki Masao, Noiri Eisei, Horinouchi Tomoko, Kaito Hiroshi, Hamada Riku, Okamoto Takayuki, Kamei Koichi, Kaku Yoshitsugu, Fujimaru Rika, Tanaka Ryojiro, Shima Yuko, , Baek Jiwon, Kang Hee Gyung, Ha Il-Soo, Han Kyoung Hee, Yang Eun Mi, , Abeyagunawardena Asiri, Lane Brandon, Chryst-Stangl Megan, Esezobor Christopher, Solarin Adaobi, , Dossier Claire, Deschênes Georges, , Vivarelli Marina, Debiec Hanna, Ishikura Kenji, Matsuo Masafumi, Nozu Kandai, Ronco Pierre, Cheong Hae Il, Sampson Matthew G, Tokunaga Katsushi, Iijima Kazumo |
| The Associations of Single Nucleotide Polymorphisms with Risk and Symptoms of Irritable Bowel Syndrome. Journal of personalized medicine 2022 Jan 12 (2): . Zhao Tingting, Zhang Yiming, Lee Joochul, Starkweather Angela R, Young Erin E, Cong Xiaom |
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