Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: MEOX2[original query] |
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| Multiple genetic loci modulate lung adenocarcinoma clinical staging. Clinical cancer research : an official journal of the American Association for Cancer Research 2011 Apr 17 (8): 2410-6. Frullanti Elisa, Galvan Antonella, Falvella Felicia S, Manenti Giacomo, Colombo Francesca, Vannelli Alberto, Incarbone Matteo, Alloisio Marco, Nosotti Mario, Santambrogio Luigi, Gonzalez-Neira Anna, Pastorino Ugo, Dragani Tommaso |
Genome-wide association study of kidney function decline in individuals of European descent.
Kidney international 2015 May 87 (5): 1017-29. Gorski Mathias, Tin Adrienne, Garnaas Maija, McMahon Gearoid M, Chu Audrey Y, Tayo Bamidele O, Pattaro Cristian, Teumer Alexander, Chasman Daniel I, Chalmers John, Hamet Pavel, Tremblay Johanne, Woodward Marc, Aspelund Thor, Eiriksdottir Gudny, Gudnason Vilmundur, Harris Tamara B, Launer Lenore J, Smith Albert V, Mitchell Braxton D, O'Connell Jeffrey R, Shuldiner Alan R, Coresh Josef, Li Man, Freudenberger Paul, Hofer Edith, Schmidt Helena, Schmidt Reinhold, Holliday Elizabeth G, Mitchell Paul, Wang Jie Jin, de Boer Ian H, Li Guo, Siscovick David S, Kutalik Zoltan, Corre Tanguy, Vollenweider Peter, Waeber Gérard, Gupta Jayanta, Kanetsky Peter A, Hwang Shih-Jen, Olden Matthias, Yang Qiong, de Andrade Mariza, Atkinson Elizabeth J, Kardia Sharon L R, Turner Stephen T, Stafford Jeanette M, Ding Jingzhong, Liu Yongmei, Barlassina Cristina, Cusi Daniele, Salvi Erika, Staessen Jan A, Ridker Paul M, Grallert Harald, Meisinger Christa, Müller-Nurasyid Martina, Krämer Bernhard K, Kramer Holly, Rosas Sylvia E, Nolte Ilja M, Penninx Brenda W, Snieder Harold, Fabiola Del Greco M, Franke Andre, Nöthlings Ute, Lieb Wolfgang, Bakker Stephan J L, Gansevoort Ron T, van der Harst Pim, Dehghan Abbas, Franco Oscar H, Hofman Albert, Rivadeneira Fernando, Sedaghat Sanaz, Uitterlinden André G, Coassin Stefan, Haun Margot, Kollerits Barbara, Kronenberg Florian, Paulweber Bernhard, Aumann Nicole, Endlich Karlhans, Pietzner Mike, Völker Uwe, Rettig Rainer, Chouraki Vincent, Helmer Catherine, Lambert Jean-Charles, Metzger Marie, Stengel Benedicte, Lehtimäki Terho, Lyytikäinen Leo-Pekka, Raitakari Olli, Johnson Andrew, Parsa Afshin, Bochud Murielle, Heid Iris M, Goessling Wolfram, Köttgen Anna, Kao W H Linda, Fox Caroline S, Böger Carsten |
| Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population. BMC genetics 2015 16 116. Yang Wen-Yi, Petit Thibault, Thijs Lutgarde, Zhang Zhen-Yu, Jacobs Lotte, Hara Azusa, Wei Fang-Fei, Salvi Erika, Citterio Lorena, Delli Carpini Simona, Gu Yu-Mei, Knez Judita, Cauwenberghs Nicholas, Barcella Matteo, Barlassina Cristina, Manunta Paolo, Coppiello Giulia, Aranguren Xabier L, Kuznetsova Tatiana, Cusi Daniele, Verhamme Peter, Luttun Aernout, Staessen Jan |
| Epigenomic study identifies a novel mesenchyme homeobox2-GLI1 transcription axis involved in cancer drug resistance, overall survival and therapy prognosis in lung cancer patients. Oncotarget 2017 Sep 8 (40): 67056-67081. Armas-López Leonel, Piña-Sánchez Patricia, Arrieta Oscar, de Alba Enrique Guzman, Ortiz-Quintero Blanca, Santillán-Doherty Patricio, Christiani David C, Zúñiga Joaquín, Ávila-Moreno Federi |
| Association of MEOX2 polymorphism with nonsyndromic cleft palate only in a Vietnamese population. Congenital anomalies 2017 Oct . Tran Duy L, Imura Hideto, Mori Akihiro, Suzuki Satoshi, Niimi Teruyuki, Ono Maya, Sakuma Chisato, Nakahara Shinichi, Nguyen Tham T H, Pham Phuong T, Hoang Viet, Tran Van T T, Nguyen Minh D, Natsume Naga |
| Mutational burden and potential oligogenic model of TBX6-mediated genes in congenital scoliosis. Molecular genetics & genomic medicine 2020 8 8 (10): e1453. Yang Yang, Zhao Sen, Zhang Yuanqiang, Wang Shengru, Shao Jiashen, Liu Bowen, Li Yaqi, Yan Zihui, Niu Yuchen, Li Xiaoxin, Wang Lianlei, Ye Yongyu, Weng Xisheng, Wu Zhihong, , Zhang Jianguo, Wu N |
| Failure to EGFR-TKI-based therapy and tumoural progression are promoted by MEOX2/GLI1-mediated epigenetic regulation of EGFR in the human lung cancer. European journal of cancer (Oxford, England : 1990) 2021 Nov . Peralta-Arrieta Irlanda, Trejo-Villegas Octavio A, Armas-López Leonel, Ceja-Rangel Hugo A, Ordóñez-Luna María Del Carmen, Pineda-Villegas Priscila, González-López Marco A, Ortiz-Quintero Blanca, Mendoza-Milla Criselda, Zatarain-Barrón Zyanya L, Arrieta Oscar, Zúñiga Joaquín, Ávila-Moreno Federi |
| Functional annotation and investigation of the 10q24.33 melanoma risk locus identifies a common variant that influences transcriptional regulation of OBFC1. Human molecular genetics 2021 Oct . Cardinale Antonella, Cantalupo Sueva, Lasorsa Vito Alessandro, Montella Annalaura, Cimmino Flora, Succoio Mariangela, Vermeulen Michiel, Baltissen Marijke P, Esposito Matteo, Avitabile Marianna, Formicola Daniela, Testori Alessandro, Bonfiglio Ferdinando, Ghiorzo Paola, Scalvenzi Massimiliano, Ayala Fabrizio, Zambrano Nicola, Iles Mark M, Xu Mai, Law Matthew H, Brown Kevin M, Iolascon Achille, Capasso Mar |
| Long noncoding RNA NRAV in the 12q24.31 risk locus drives gastric cancer development through glucose metabolism reprogramming. Carcinogenesis 2023 11 . Yan Zhang, Yun Gao, Fengyuan Li, Qi Qi, Qian Li, Yuanliang Gu, Zhonghua Zheng, Beiping Hu, Tianpei Wang, Erbao Zhang, Hao Xu, Li Liu, Tian Tian, Guangfu Jin, Caiwang Y |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 04, 2023
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