Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: ADD3[original query] |
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Role of the adducin family genes in human essential hypertension. Journal of hypertension 2005 Mar 23 (3): 543-9. Lanzani Chiara, Citterio Lorena, Jankaricova Maria, Sciarrone M Teresa, Barlassina Cristina, Fattori Stefania, Messaggio Elisabetta, Serio Clelia Di, Zagato Laura, Cusi Daniele, Hamlyn John M, Stella Alessandra, Bianchi Giuseppe, Manunta Pao |
Arterial properties in relation to genetic variations in the adducin subunits in a white population. American journal of hypertension 2009 Jan 22 (1): 21-6. Seidlerová Jitka, Staessen Jan A, Bochud Murielle, Nawrot Tim, Casamassima Nunzia, Citterio Lorena, Kuznetsova Tatiana, Jin Yu, Manunta Paulo, Richart Tom, Struijker-Boudier Harry A, Fagard Robert, Filipovský Jan, Bianchi Giusep |
Gly460Trp alpha-adducin mutation as a possible mechanism leading to endolymphatic hydrops in Ménière's syndrome. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2008 Sep 29 (6): 824-8. Teggi Roberto, Lanzani Chiara, Zagato Laura, Delli Carpini Simona, Manunta Paolo, Bianchi Giuseppe, Bussi Mar |
Effects of genetic variation in adducin on left ventricular diastolic function as assessed by tissue Doppler imaging in a Flemish population. Journal of hypertension 2008 Jun 26 (6): 1229-36. Kuznetsova Tatiana, Citterio Lorena, Herbots Lieven, Carpini Simona Delli, Thijs Lutgarde, Casamassima Nunzia, Richart Tom, Fagard Robert H, Bianchi Giuseppe, Staessen Jan |
Deletions of IKZF1 and SPRED1 are associated with poor prognosis in a population-based series of pediatric B-cell precursor acute lymphoblastic leukemia diagnosed between 1992 and 2011. Leukemia 2014 Feb 28 (2): 302-10. Olsson L, Castor A, Behrendtz M, Biloglav A, Forestier E, Paulsson K, Johansson |
Common genetic variants regulating ADD3 gene expression alter biliary atresia risk. Journal of hepatology 2013 Dec 59 (6): 1285-91. Cheng Guo, Tang Clara Sze-Man, Wong Emily Hoi-Man, Cheng William Wai-Chun, So Man-Ting, Miao Xiaoping, Zhang Ruizhong, Cui Long, Liu Xuelai, Ngan Elly Sau-Wai, Lui Vincent Chi-Hang, Chung Patrick Ho-Yu, Chan Ivy Hau-Yee, Liu Juncheng, Zhong Wei, Xia Huimin, Yu Jiakang, Qiu Xiu, Wu Xuan-Zhao, Wang Bin, Dong Xiao, Tou Jinfa, Huang Liuming, Yi Bin, Ren Hongxia, Chan Edwin Kin-Wai, Ye Kenny, O'Reilly Paul F, Wong Kenneth Kak-Yuen, Sham Pak-Chung, Cherny Stacey S, Tam Paul Kwong-Hang, Garcia-Barceló Maria-Mer |
Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia. Human genetics 2014 Feb 133 (2): 235-43. Tsai Ellen A, Grochowski Christopher M, Loomes Kathleen M, Bessho Kazuhiko, Hakonarson Hakon, Bezerra Jorge A, Russo Pierre A, Haber Barbara A, Spinner Nancy B, Devoto Marcel |
Association between single nucleotide polymorphisms in the ADD3 gene and susceptibility to biliary atresia. PloS one 2014 9 (10): e107977. Zeng Shuaidan, Sun Peng, Chen Zimin, Mao Jianxiong, Wang Jianyao, Wang Bin, Liu L |
Alpha Adducin G460T Variant is a Risk Factor for Hypertension in Tunisian Population. Clinical laboratory 2016 62 (5): 765-70. Soualmia Hayet, Ben Romdhane Abir, Midani Fatma, Kallel Amani, Jemaa Riadh, Feki Moncef, Kaabachi Nazi |
Characterisation of the genomic landscape of CRLF2-rearranged acute lymphoblastic leukemia. Genes, chromosomes & cancer 2016 Dec . Russell Lisa J, Jones Lisa, Enshaei Amir, Tonin Stefano, Ryan Sarra L, Eswaran Jeyanthy, Nakjang Sirintra, Papaemmanuil Elli, Tubio Jose M C, Fielding Adele K, Vora Ajay, Campbell Peter J, Moorman Anthony V, Harrison Christine |
Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder.
Translational psychiatry 2017 Jan 7 (1): e993. Charney A W, Ruderfer D M, Stahl E A, Moran J L, Chambert K, Belliveau R A, Forty L, Gordon-Smith K, Di Florio A, Lee P H, Bromet E J, Buckley P F, Escamilla M A, Fanous A H, Fochtmann L J, Lehrer D S, Malaspina D, Marder S R, Morley C P, Nicolini H, Perkins D O, Rakofsky J J, Rapaport M H, Medeiros H, Sobell J L, Green E K, Backlund L, Bergen S E, Juréus A, Schalling M, Lichtenstein P, Roussos P, Knowles J A, Jones I, Jones L A, Hultman C M, Perlis R H, Purcell S M, McCarroll S A, Pato C N, Pato M T, Craddock N, Landén M, Smoller J W, Sklar |
The utilization of next-generation sequencing to detect somatic mutations and predict clinical prognosis of Chinese non-small cell lung cancer patients. OncoTargets and therapy 2018 11 2637-2646. Cao Liming, Long Long, Li Min, Yang Huaping, Deng Pengbo, Mao Xinru, Xiang Jianxing, Li Bing, Zhang Tengfei, Hu Chengpi |
The intragenic epistatic association of ADD3 with biliary atresia in Southern Han Chinese population. Bioscience reports 2018 Apr . Wang Zhe, Xie Xiaoli, Zhao Jinglu, Fu Ming, Li Yonglan, Zhong Wei, Xia Huimin, Zhang Yan, Zhang Rui-Zho |
Single nucleotide polymorphisms within Adducin 3 and Adducin 3 antisense RNA1 genes are associated with biliary atresia in Thai infants. Pediatric surgery international 2018 Mar . Laochareonsuk Wison, Chiengkriwate Piyawan, Sangkhathat Suras |
Association of common variation in ADD3 and GPC1 with biliary atresia susceptibility. Aging 2020 4 12 (8): 7163-7182. Bai Mei-Rong, Niu Wei-Bo, Zhou Ying, Gong Yi-Ming, Lu Yan-Jiao, Yu Xian-Xian, Wei Zhi-Liang, Wu Wenjie, Song Huan-Lei, Yu Wen-Wen, Gu Bei-Lin, Cai Wei, Chu X |
ADD3 Deletion in Glioblastoma Predicts Disease Status and Survival. Frontiers in oncology 2021 12 11 717793. Kiang Karrie Mei-Yee, Sun Stella, Leung Gilberto Ka-K |
Impact of EFEMP1 on the survival outcome of biliary atresia in Thai infants. Scientific reports 2022 Sep 12 (1): 15603. Laochareonsuk Wison, Kayasut Kanita, Surachat Komwit, Chiengkriwate Piyawan, Sangkhathat Suras |
Contribution of ADD3 and the HLA Genes to Biliary Atresia Risk in Chinese. International journal of molecular sciences 2023 10 24 (19): . Meng-Meng Cui, Yi-Ming Gong, Wei-Hua Pan, Hao-Yue Pei, Mei-Rong Bai, Huan-Lei Song, Xin-Ru Han, Wen-Jie Wu, Wen-Wen Yu, Bei-Lin Gu, Wei Cai, Ying Zhou, Xun C |
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- Page last updated:Apr 22, 2024
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