Human Genome Epidemiology Literature Finder
Records 1 - 24 (of 24 Records) |
Query Trace: TFAP2A[original query] |
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Genes encoding critical transcriptional activators for murine neural tube development and human spina bifida: a case-control study. BMC medical genetics 2010 11 141. Lu Wei, Guzman Adrian R, Yang Wei, Chapa Claudia J, Shaw Gary M, Greene Robert M, Pisano M Michele, Lammer Edward J, Finnell Richard H, Zhu Huipi |
Single-nucleotide polymorphisms (SNPs) of the IRF6 and TFAP2A in non-syndromic cleft lip with or without cleft palate (NSCLP) in a northern Chinese population. Biochemical and biophysical research communications 2011 Jul 410 (4): 732-6. Shi Jinna, Song Tao, Jiao Xiaohui, Qin Chunlin, Zhou J |
MDM2 promoter SNP344T>A (rs1196333) status does not affect cancer risk. PloS one 2012 7 (4): e36263. Knappskog Stian, Gansmo Liv B, Romundstad Pål, Bjørnslett Merete, Trovik Jone, Sommerfelt-Pettersen Jan, Løkkevik Erik, , Tollenaar Rob A E M, Seynaeve Caroline, Devilee Peter, Salvesen Helga B, Dørum Anne, Hveem Kristian, Vatten Lars, Lønning Per |
Potential association of DCBLD2 polymorphisms with fall rates of FEV(1) by aspirin provocation in Korean asthmatics. Journal of Korean medical science 2012 Apr 27 (4): 343-9. Park Tae-Joon, Kim Jeong-Hyun, Park Byung-Lae, Cheong Hyun Sub, Bae Joon Seol, Pasaje Charisse F, Park Jong-Sook, Uh Soo-Taek, Kim Mi-Kyeong, Choi Inseon S, Park Choon-Sik, Shin Hyoung D |
Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes. American journal of medical genetics. Part A 2013 Oct 161A (10): 2535-44. Leslie Elizabeth J, Mancuso Jennifer L, Schutte Brian C, Cooper Margaret E, Durda Kate M, L'heureux Jamie, Zucchero Theresa M, Marazita Mary L, Murray Jeffrey |
Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk.
PLoS genetics 2013 9 (3): e1003173. Gaudet Mia M, Kuchenbaecker Karoline B, Vijai Joseph, Klein Robert J, Kirchhoff Tomas, McGuffog Lesley, Barrowdale Daniel, Dunning Alison M, Lee Andrew, Dennis Joe, Healey Sue, Dicks Ed, Soucy Penny, Sinilnikova Olga M, Pankratz Vernon S, Wang Xianshu, Eldridge Ronald C, Tessier Daniel C, Vincent Daniel, Bacot Francois, Hogervorst Frans B L, Peock Susan, Stoppa-Lyonnet Dominique, , Peterlongo Paolo, Schmutzler Rita K, Nathanson Katherine L, Piedmonte Marion, Singer Christian F, Thomassen Mads, , Hansen Thomas v O, Neuhausen Susan L, Blanco Ignacio, Greene Mark H, Garber Judith, Weitzel Jeffrey N, Andrulis Irene L, Goldgar David E, D'Andrea Emma, Caldes Trinidad, Nevanlinna Heli, Osorio Ana, van Rensburg Elizabeth J, Arason Adalgeir, Rennert Gad, van den Ouweland Ans M W, van der Hout Annemarie H, Kets Carolien M, Aalfs Cora M, Wijnen Juul T, Ausems Margreet G E M, , , Frost Debra, Ellis Steve, Fineberg Elena, Platte Radka, Evans D Gareth, Jacobs Chris, Adlard Julian, Tischkowitz Marc, Porteous Mary E, Damiola Francesca, , Golmard Lisa, Barjhoux Laure, Longy Michel, Belotti Muriel, Ferrer Sandra Fert, Mazoyer Sylvie, Spurdle Amanda B, Manoukian Siranoush, Barile Monica, Genuardi Maurizio, Arnold Norbert, Meindl Alfons, Sutter Christian, Wappenschmidt Barbara, Domchek Susan M, Pfeiler Georg, Friedman Eitan, Jensen Uffe Birk, Robson Mark, Shah Sohela, Lazaro Conxi, Mai Phuong L, Benitez Javier, Southey Melissa C, Schmidt Marjanka K, Fasching Peter A, Peto Julian, Humphreys Manjeet K, Wang Qin, Michailidou Kyriaki, Sawyer Elinor J, Burwinkel Barbara, Guénel Pascal, Bojesen Stig E, Milne Roger L, Brenner Hermann, Lochmann Magdalena, , Aittomäki Kristiina, Dörk Thilo, Margolin Sara, Mannermaa Arto, Lambrechts Diether, Chang-Claude Jenny, Radice Paolo, Giles Graham G, Haiman Christopher A, Winqvist Robert, Devillee Peter, García-Closas Montserrat, Schoof Nils, Hooning Maartje J, Cox Angela, Pharoah Paul D P, Jakubowska Anna, Orr Nick, González-Neira Anna, Pita Guillermo, Alonso M Rosario, Hall Per, Couch Fergus J, Simard Jacques, Altshuler David, Easton Douglas F, Chenevix-Trench Georgia, Antoniou Antonis C, Offit Kenne |
Whole exome sequence analysis of Peters anomaly. Human genetics 2014 Dec 133 (12): 1497-511. Weh Eric, Reis Linda M, Happ Hannah C, Levin Alex V, Wheeler Patricia G, David Karen L, Carney Erin, Angle Brad, Hauser Natalie, Semina Elena |
Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium.
Diabetes 2015 May 64 (5): 1853-66. Palmer Nicholette D, Goodarzi Mark O, Langefeld Carl D, Wang Nan, Guo Xiuqing, Taylor Kent D, Fingerlin Tasha E, Norris Jill M, Buchanan Thomas A, Xiang Anny H, Haritunians Talin, Ziegler Julie T, Williams Adrienne H, Stefanovski Darko, Cui Jinrui, Mackay Adrienne W, Henkin Leora F, Bergman Richard N, Gao Xiaoyi, Gauderman James, Varma Rohit, Hanis Craig L, Cox Nancy J, Highland Heather M, Below Jennifer E, Williams Amy L, Burtt Noel P, Aguilar-Salinas Carlos A, Huerta-Chagoya Alicia, Gonzalez-Villalpando Clicerio, Orozco Lorena, Haiman Christopher A, Tsai Michael Y, Johnson W Craig, Yao Jie, Rasmussen-Torvik Laura, Pankow James, Snively Beverly, Jackson Rebecca D, Liu Simin, Nadler Jerry L, Kandeel Fouad, Chen Yii-Der I, Bowden Donald W, Rich Stephen S, Raffel Leslie J, Rotter Jerome I, Watanabe Richard M, Wagenknecht Lynne |
A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population. Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery 2015 Aug . Araujo Tânia Kawasaki de, Secolin Rodrigo, Félix Têmis Maria, Souza Liliane Todeschini de, Fontes Marshall Ítalo Barros, Monlleó Isabella Lopes, Souza Josiane de, Fett-Conte Agnes Cristina, Ribeiro Erlane Marques, Xavier Ana Carolina, Rezende Adriana Augusto de, Simioni Milena, Ribeiro-Dos-Santos Ândrea Kely Campos, Santos Sidney Emanuel Batista Dos, Gil-da-Silva-Lopes Vera Lúc |
Association of TFAP2A gene polymorphism with susceptibility to non-syndromic cleft lip with or without palate risk in south Indian population. Meta gene 2016 Sep 9 181-4. Babu Gurramkonda Venkatesh, Syed Altaf Hussain, Murthy Jyotsna, V K S Lakkakula Bhask |
MiR-193a-5p Targets the Coding Region of AP-2a mRNA and Induces Cisplatin Resistance in Bladder Cancers. Journal of Cancer 2016 7 (12): 1740-1746. Zhou Ji, Duan Huaxin, Xie Yu, Ning Yichong, Zhang Xing, Hui Na, Wang Chunqing, Zhang Jian, Zhou Jianl |
DNA hypomethylation of a transcription factor binding site within the promoter of a gout risk gene NRBP1 upregulates its expression by inhibition of TFAP2A binding. Clinical epigenetics 2017 9 99. Zhu Zaihua, Meng Weida, Liu Peiru, Zhu Xiaoxia, Liu Yun, Zou Heji |
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.
Nature communications 2017 Feb 8 14364. Yu Yanqin, Zuo Xianbo, He Miao, Gao Jinping, Fu Yuchuan, Qin Chuanqi, Meng Liuyan, Wang Wenjun, Song Yaling, Cheng Yong, Zhou Fusheng, Chen Gang, Zheng Xiaodong, Wang Xinhuan, Liang Bo, Zhu Zhengwei, Fu Xiazhou, Sheng Yujun, Hao Jiebing, Liu Zhongyin, Yan Hansong, Mangold Elisabeth, Ruczinski Ingo, Liu Jianjun, Marazita Mary L, Ludwig Kerstin U, Beaty Terri H, Zhang Xuejun, Sun Liangdan, Bian Zhu |
LncRNA GAS5 Indel Genetic Polymorphism Contributes to Glioma Risk Through Interfering Binding of Transcriptional Factor TFAP2A. DNA and cell biology 2018 Aug . Yuan Jupeng, Zhang Nasha, Zheng Yan, Chen Yi-Dong, Liu Jie, Yang Mi |
A functional CNVR_3425.1 damping lincRNA FENDRR increases lifetime risk of lung cancer and COPD in Chinese. Carcinogenesis 2018 1 39 (3): 347-359. Yang Lei, Wu Di, Chen Jinbin, Chen Jiansong, Qiu Fuman, Li Yinyan, Liu Li, Cao Yi, Yang Binyao, Zhou Yifeng, Lu Jiach |
Novel Myopia Genes and Pathways Identified From Syndromic Forms of Myopia. Investigative ophthalmology & visual science 2018 1 59 (1): 338-348. Flitcroft D Ian, Loughman James, Wildsoet Christine F, Williams Cathy, Guggenheim Jeremy A, |
Target Capture/Next-Generation Sequencing for Nonsyndromic Cleft Lip and Palate in the Japanese Population. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2019 7 57 (1): 80-87. Shibano Masayasu, Watanabe Akira, Takano Nobuo, Mishima Hiroyuki, Kinoshita Akira, Yoshiura Koh-Ichiro, Shibahara Takahi |
A functional indel polymorphism rs34396413 in TFAP2A intron-5 significantly increases female encephalocele risk in Han Chinese population. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2019 Apr . Su Ke, Chen Shuxia, Ye Jianhong, Kuang Lele, Zhang Ting, Wang Hongyan, Yang Xuey |
DACT2 modulated by TFAP2A-mediated allelic transcription promotes EGFR-TKIs efficiency in advanced lung adenocarcinoma. Biochemical pharmacology 2019 Dec 113772. Zhang Nasha, Li Yankang, Xie Mengyu, Song Yemei, Liu Jiandong, Lei Tianshui, Shen Yue, Yu Jinming, Yang Mi |
Family based and case-control designs reveal an association of TFAP2A in nonsyndromic cleft lip only among Vietnamese population. Molecular genetics & genomic medicine 2021 Jul e1754. Nguyen Duc Minh, Suzuki Satoshi, Imura Hideto, Niimi Teruyuki, Furukawa Hiroo, Ta Thanh-Van, Tong Son Minh, Nguyen Tra Thu, Pham Loc Nguyen Gia, Tran Duy Le, Natsume Naga |
Polymorphism of rs6426749 at 1p36.12 is associated with the risk of osteoarthritis in Taiwanese female population. Journal of the Chinese Medical Association : JCMA 2021 Mar . Tsai Dung-Jang, Tai Ming-Cheng, Kao Chung-Cheng, Chen Wei-Teing, Wu Li-Wei, Chiu Chih-Chien, Tu Ming-Yu, Chen Yi-Chou, Wu Chia-Chun, Su Sui-Lu |
Allele-specific transcription factor binding in a cellular model of orofacial clefting. Scientific reports 2022 2 12 (1): 1807. Ruff Katharina L M, Hollstein Ronja, Fazaal Julia, Thieme Frederic, Gehlen Jan, Mangold Elisabeth, Knapp Michael, Welzenbach Julia, Ludwig Kerstin |
A novel prognostic signature based on N7-methylguanosine-related long non-coding RNAs in breast cancer. Frontiers in genetics 2022 10 13 1030275. Huang Zhidong, Lou Kaixin, Liu Ho |
Transcriptional repression and apoptosis influence the effect of APOBEC3A/3B functional polymorphisms on biliary tract cancer risk. International journal of cancer 2022 1 150 (11): 1825-1837. Liu Wenbin, Ji Hongxiang, Zhao Jun, Song Jiahui, Zheng Shaoling, Chen Lei, Li Peng, Tan Xiaojie, Ding Yibo, Pu Rui, Yin Jianhua, Han Xue, Cao Guangw |
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