Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: SLC9A3[original query] |
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Genetic susceptibility to febrile seizures: case-control association studies. Brain & development 2010 Jan 32 (1): 57-63. Kira Ryutaro, Ishizaki Yoshito, Torisu Hiroyuki, Sanefuji Masafumi, Takemoto Megumi, Sakamoto Kanji, Matsumoto Shigetaka, Yamaguchi Yui, Yukaya Naoko, Sakai Yasunari, Gondo Kenjiro, Hara Toshi |
Genetic variation in solute carrier genes is associated with preeclampsia. American journal of obstetrics and gynecology 2010 Nov 203 (5): 491.e1-491.e13. Morrison Alanna C, Srinivas Sindhu K, Elovitz Michal A, Puschett Jules |
Modulatory effect of the SLC9A3 gene on susceptibility to infections and pulmonary function in children with cystic fibrosis. Pediatric pulmonology 2011 Apr 46 (4): 385-92. Dorfman Ruslan, Taylor Chelsea, Lin Fan, Sun Lei, Sandford Andrew, Paré Peter, Berthiaume Yves, Corey Mary, Durie Peter, Zielenski Julian, |
Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis. Nature genetics 2012 May 44 (5): 562-9. Sun Lei, Rommens Johanna M, Corvol Harriet, Li Weili, Li Xin, Chiang Theodore A, Lin Fan, Dorfman Ruslan, Busson Pierre-François, Parekh Rashmi V, Zelenika Diana, Blackman Scott M, Corey Mary, Doshi Vishal K, Henderson Lindsay, Naughton Kathleen M, O'Neal Wanda K, Pace Rhonda G, Stonebraker Jaclyn R, Wood Sally D, Wright Fred A, Zielenski Julian, Clement Annick, Drumm Mitchell L, Boëlle Pierre-Yves, Cutting Garry R, Knowles Michael R, Durie Peter R, Strug Lisa |
Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities. Human genetics 2014 Feb 133 (2): 151-61. Li Weili, Soave David, Miller Melissa R, Keenan Katherine, Lin Fan, Gong Jiafen, Chiang Theodore, Stephenson Anne L, Durie Peter, Rommens Johanna, Sun Lei, Strug Lisa |
Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis.
Nature communications 2015 Sep 6 8382. Corvol Harriet, Blackman Scott M, Boëlle Pierre-Yves, Gallins Paul J, Pace Rhonda G, Stonebraker Jaclyn R, Accurso Frank J, Clement Annick, Collaco Joseph M, Dang Hong, Dang Anthony T, Franca Arianna, Gong Jiafen, Guillot Loic, Keenan Katherine, Li Weili, Lin Fan, Patrone Michael V, Raraigh Karen S, Sun Lei, Zhou Yi-Hui, O'Neal Wanda K, Sontag Marci K, Levy Hara, Durie Peter R, Rommens Johanna M, Drumm Mitchell L, Wright Fred A, Strug Lisa J, Cutting Garry R, Knowles Michael |
Association of clinical severity of cystic fibrosis with variants in the SLC gene family (SLC6A14, SLC26A9, SLC11A1 and SLC9A3). Gene 2017 7 629 117-126. Pereira Stéphanie Villa-Nova, Ribeiro José Dirceu, Bertuzzo Carmen Sílvia, Marson Fernando Augusto Li |
A common NHE3 single-nucleotide polymorphism has normal function and sensitivity to regulatory ligands. American journal of physiology. Gastrointestinal and liver physiology 2017 May ajpgi.00044.2017. Yin Jianyi, Tse Chung-Ming, Cha Boyoung, Sarker Rafiqual, Zhu Xinjun C, Walentinsson Anna, Greasley Peter J, Donowitz Ma |
Polymorphisms in Renal Ammonia Metabolism Genes Correlate With 24-Hour Urine pH. Kidney international reports 2017 Nov 2 (6): 1111-1121. Canales Benjamin K, Smith Jennifer A, Weiner I David, Ware Erin B, Zhao Wei, Kardia Sharon L R, Curhan Gary C, Turner Stephen T, Perinpam Majuran, Lieske John |
Interaction among variants in the SLC gene family (SLC6A14, SLC26A9, SLC11A1, and SLC9A3) and CFTR mutations with clinical markers of cystic fibrosis. Pediatric pulmonology 2018 4 53 (7): 888-900. Pereira Stephanie V N, Ribeiro Jose D, Bertuzzo Carmen S, Marson Fernando A |
SLC9A3 Affects Vas Deferens Development and Associates with Taiwanese Congenital Bilateral Absence of the Vas Deferens. BioMed research international 2019 4 2019 3562719. Wu Yi-No, Chen Kuo-Chiang, Wu Chien-Chih, Lin Ying-Hung, Chiang Han-S |
Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies. International journal of molecular sciences 2020 1 21 (2): . Gianesello Lisa, Ceol Monica, Bertoldi Loris, Terrin Liliana, Priante Giovanna, Murer Luisa, Peruzzi Licia, Giordano Mario, Paglialonga Fabio, Cantaluppi Vincenzo, Musetti Claudio, Valle Giorgio, Del Prete Dorella, Anglani Franca, Network Dent Disease Itali |
Identification of loci of functional relevance to Barrett's esophagus and esophageal adenocarcinoma: Cross-referencing of expression quantitative trait loci data from disease-relevant tissues with genetic association data. PloS one 2020 1 14 (12): e0227072. Schröder Julia, Schüller Vitalia, May Andrea, Gerges Christian, Anders Mario, Becker Jessica, Hess Timo, Kreuser Nicole, Thieme René, Ludwig Kerstin U, Noder Tania, Venerito Marino, Veits Lothar, Schmidt Thomas, Fuchs Claudia, Izbicki Jakob R, Hölscher Arnulf H, Dakkak Dani, Jansen-Winkeln Boris, Moulla Yusef, Lyros Orestis, Niebisch Stefan, Mehdorn Matthias, Lang Hauke, Lorenz Dietmar, Schumacher Brigitte, Mayershofer Rupert, Vashist Yogesh, Ott Katja, Vieth Michael, Weismüller Josef, Mangold Elisabeth, Nöthen Markus M, Moebus Susanne, Knapp Michael, Neuhaus Horst, Rösch Thomas, Ell Christian, Gockel Ines, Schumacher Johannes, Böhmer Anne |
Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study†. Biology of reproduction 2021 Oct . Tan Mao-Qing, Huang Wu-Jian, Lan Feng-Hua, Xu Yong-Jun, Zheng Mei-Yu, Tang Yi |
Risk factors for Pseudomonas aeruginosa airway infection and lung function decline in children with cystic fibrosis. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2021 10 21 (1): 45-51. Mésinèle Julie, Ruffin Manon, Kemgang Astrid, Guillot Loïc, Boëlle Pierre-Yves, Corvol Harri |
Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole Genome Analysis of 7,840 Patients.
American journal of respiratory and critical care medicine 2023 3 . Zhou Yi-Hui, Gallins Paul J, Pace Rhonda G, Dang Hong, Aksit Melis A, Blue Elizabeth E, Buckingham Kati J, Collaco Joseph M, Faino Anna V, Gordon William W, Hetrick Kurt N, Ling Hua, Liu Weifang, Onchiri Frankline M, Pagel Kymberleigh, Pugh Elizabeth W, Raraigh Karen S, Rosenfeld Margaret, Sun Quan, Wen Jia, Li Yun, Corvol Harriet, Strug Lisa J, Bamshad Michael J, Blackman Scott M, Cutting Garry R, Gibson Ronald L, O'Neal Wanda K, Wright Fred A, Knowles Michael |
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