Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: AQP2[original query] |
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Correlation between AVPR2 mutations and urinary AQP2 excretion in patients with nephrogenic diabetes insipidus. Journal of pediatric endocrinology & metabolism : JPEM 2007 Apr 20 (4): 483-9. Kotnik Primoz, Battelino Tadej, Debeljak Marusa, Podkrajsek Katarina Trebusak, Waldhauser Franz, Frøkiaer Jørgen, Nielsen Søren, Krzisnik Cir |
Genetic predisposition and nongenetic risk factors of thiazolidinedione-related edema in patients with type 2 diabetes. Pharmacogenetics and genomics 2011 Dec 21 (12): 829-36. Chang Tien-Jyun, Liu Pi-Hua, Liang Yi-Chi, Chang Yi-Cheng, Jiang Yi-Der, Li Hung-Yuan, Lo Min-Tzu, Chen Harn-Shen, Chuang Lee-Mi |
Influence of aquaporin-1 gene polymorphism on water retention in liver cirrhosis. Scandinavian journal of gastroenterology 2011 Oct 46 (10): 1267-74. Fábrega Emilio, Berja Ana, García-Unzueta María Teresa, Guerra-Ruiz Armando, Cobo Marta, López María, Bolado-Carrancio Alfonso, Amado José Antonio, Rodríguez-Rey José Carlos, Pons-Romero Fernan |
A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies. International journal of audiology 2012 Aug . Hietikko E, Kotimäki J, Okuloff A, Sorri M, Männikkö M |
The association of transporter genes polymorphisms and lung cancer chemotherapy response. PloS one 2014 9 (3): e91967. Wang Ying, Yin Ji-Ye, Li Xiang-Ping, Chen Juan, Qian Chen-Yue, Zheng Yi, Fu Yi-Lan, Chen Zi-Yu, Zhou Hong-Hao, Liu Zhao-Qi |
Effect of transporter and DNA repair gene polymorphisms to lung cancer chemotherapy toxicity. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Sep . Chen Juan, Wu Lin, Wang Ying, Yin Jiye, Li Xiangping, Wang Zhan, Li Huihua, Zou Ting, Qian Chenyue, Li Chuntian, Zhang Wei, Zhou Honghao, Liu Zhaoqi |
Aquaporin 5 Interacts with Fluoride and Possibly Protects against Caries. PloS one 0 10 (12): e0143068. Anjomshoaa Ida, Briseño-Ruiz Jessica, Deeley Kathleen, Poletta Fernardo A, Mereb Juan C, Leite Aline L, Barreta Priscila A T M, Silva Thelma L, Dizak Piper, Ruff Timothy, Patir Asli, Koruyucu Mine, Abbaso?lu Zerrin, Casado Priscila L, Brown Andrew, Zaky Samer H, Bayram Merve, Küchler Erika C, Cooper Margaret E, Liu Kai, Marazita Mary L, Tanbo?a ?lknur, Granjeiro José M, Seymen Figen, Castilla Eduardo E, Orioli Iêda M, Sfeir Charles, Owyang Hongjiao, Buzalaf Marília A R, Vieira Alexandre |
Ménière's Disease: Molecular Analysis of Aquaporins 2, 3 and Potassium Channel KCNE1 Genes in Brazilian Patients. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2016 09 37 (8): 1117-21. Lopes Karen de Carvalho, Sartorato Edi Lúcia, da Silva-Costa Sueli M, de Macedo Adamov Nadya Soares, Ganança Fernando Freit |
Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant). Best practice & research. Clinical endocrinology & metabolism 2016 Mar 30 (2): 263-76. Bichet Daniel G, Bockenhauer Detl |
PNPLA3 Association with Alcoholic Liver Disease in a Cohort of Heavy Drinkers. Alcohol and alcoholism (Oxford, Oxfordshire) 2018 Feb . Kolla Bhanu Prakash, Schneekloth Terry D, Biernacka Joanna, Shah Vijay, Lazaridis Konstantinos N, Geske Jennifer, Karpyak Vict |
[Genetic Predisposition to Early Myocardial Infarction]. Molekuliarnaia biologiia 0 54 (2): 224-232. Goncharova I A, Nazarenko M S, Babushkina N P, Markov A V, Pecherina T B, Kashtalap V V, Tarasenko N V, Ponasenko A V, Barbarash O L, Puzyrev V |
Aquaporin locus (12q13.12) might contribute to susceptibility of temporomandibular joint disorder associated with periodontitis. PloS one 2020 3 15 (3): e0229245. Bezamat Mariana, Cunha Emanuelle J, Modesto Adriana M, Vieira Alexandre R, Taboas Juan |
Aquaporins' Influence on Different Dental Erosive Wear Phenotypes in Humans. Caries research 2020 Feb 1-11. Tulek Amela, Vieira Alexandre Rezende, Weber Megan L, Bezamat Mariana, Deeley Kathleen, Stenhagen Kjersti Refsholt, Sehic Amer, Sovik Jenny Bogstad, Mulic Ai |
Novel AQP2 Mutations and Clinical Characteristics in Seven Chinese Families With Congenital Nephrogenic Diabetes Insipidus. Frontiers in endocrinology 2021 6 12 686818. Li Qian, Tian Dan, Cen Jing, Duan Lian, Xia Wei |
Integrating Population Variants and Protein Structural Analysis to Improve Clinical Genetic Diagnosis and Treatment in Nephrogenic Diabetes Insipidus. Frontiers in pediatrics 2021 5 9 566524. Liao Panli, Xiang Tianchao, Li Hongxia, Fang Ye, Fang Xiaoyan, Zhang Zhiqing, Cao Qi, Zhai Yihui, Chen Jing, Xu Linan, Liu Jialu, Tang Xiaoshan, Liu Xiaorong, Wang Xiaowen, Luan Jiangwei, Shen Qian, Chen Lizhi, Jiang Xiaoyun, Ma Duan, Xu Hong, Rao J |
A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation. BioMed research international 2022 7 2022 7073158. Zang Li, Gong Yuping, Li Yijun, Dou Jingtao, Lyu Zhaohui, Su Xiaoqing, Zhang Yawei, Mu Yimi |
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure. Kidney international reports 2023 10 8 (10): 2126-2135. Yishay Ben-Moshe, Omer Shlomovitz, Danit Atias-Varon, Orly Haskin, Efrat Ben-Shalom, Hadas Shasha Lavsky, Oded Volovelsky, Shrikant Mane, Dror Ben-Ruby, Guy Chowers, Karl Skorecki, Yael Borovitz, Maayan Kagan, Nofar Mor, Yulia Khavkin, Shimrit Tzvi-Behr, Shirley Pollack, Moran Plonsky Toder, Michael Geylis, Aviad Schnapp, Rachel Becker-Cohen, Irith Weissman, Ruth Schreiber, Miriam Davidovits, Yaacov Frishberg, Daniella Magen, Ortal Barel, Asaf Vivan |
Genes and single nucleotide polymorphisms in the pathway of saliva and dental caries: a systematic review and meta-analysis. Biofouling 2023 1 1-16. Chisini Luiz Alexandre, Varella de Carvalho Rodrigo, Dos Santos Costa Francine, Salvi Luana Carla, Demarco Flávio Fernando, Britto Correa Marc |
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