Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: ASCL1[original query] |
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Genetic association analyses of PHOX2B and ASCL1 in neuropsychiatric disorders: evidence for association of ASCL1 with Parkinson's disease. Human genetics 2005 Oct 117 (6): 520-7. Ide Masayuki, Yamada Kazuo, Toyota Tomoko, Iwayama Yoshimi, Ishitsuka Yuichi, Minabe Yoshio, Nakamura Kazuhiko, Hattori Nobutaka, Asada Takashi, Mizuno Yoshikuni, Mori Norio, Yoshikawa Tak |
Analysis of coding-polymorphisms in NOTCH-related genes reveals NUMBL poly-glutamine repeat to be associated with schizophrenia in Brazilian and Danish subjects. Schizophrenia research 2006 Dec 88 (1-3): 275-82. Passos Gregorio Sheila, Gattaz Wagner F, Tavares Hildeberto, Kieling Christian, Timm Sally, Wang August G, Berg Rasmussen Henrik, Werge Thomas, Dias-Neto Emmanu |
Genetic variation in an miRNA-1827 binding site in MYCL1 alters susceptibility to small-cell lung cancer. Cancer research 2011 Aug 71 (15): 5175-81. Xiong Fang, Wu Chen, Chang Jiang, Yu Dianke, Xu Binghe, Yuan Peng, Zhai Kan, Xu Jian, Tan Wen, Lin Dongx |
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.
Circulation 2011 Feb 123 (7): 731-8. Dehghan Abbas, Dupuis Josée, Barbalic Maja, Bis Joshua C, Eiriksdottir Gudny, Lu Chen, Pellikka Niina, Wallaschofski Henri, Kettunen Johannes, Henneman Peter, Baumert Jens, Strachan David P, Fuchsberger Christian, Vitart Veronique, Wilson James F, Paré Guillaume, Naitza Silvia, Rudock Megan E, Surakka Ida, de Geus Eco J C, Alizadeh Behrooz Z, Guralnik Jack, Shuldiner Alan, Tanaka Toshiko, Zee Robert Y L, Schnabel Renate B, Nambi Vijay, Kavousi Maryam, Ripatti Samuli, Nauck Matthias, Smith Nicholas L, Smith Albert V, Sundvall Jouko, Scheet Paul, Liu Yongmei, Ruokonen Aimo, Rose Lynda M, Larson Martin G, Hoogeveen Ron C, Freimer Nelson B, Teumer Alexander, Tracy Russell P, Launer Lenore J, Buring Julie E, Yamamoto Jennifer F, Folsom Aaron R, Sijbrands Eric J G, Pankow James, Elliott Paul, Keaney John F, Sun Wei, Sarin Antti-Pekka, Fontes João D, Badola Sunita, Astor Brad C, Hofman Albert, Pouta Anneli, Werdan Karl, Greiser Karin H, Kuss Oliver, Meyer zu Schwabedissen Henriette E, Thiery Joachim, Jamshidi Yalda, Nolte Ilja M, Soranzo Nicole, Spector Timothy D, Völzke Henry, Parker Alexander N, Aspelund Thor, Bates David, Young Lauren, Tsui Kim, Siscovick David S, Guo Xiuqing, Rotter Jerome I, Uda Manuela, Schlessinger David, Rudan Igor, Hicks Andrew A, Penninx Brenda W, Thorand Barbara, Gieger Christian, Coresh Joe, Willemsen Gonneke, Harris Tamara B, Uitterlinden Andre G, Järvelin Marjo-Riitta, Rice Kenneth, Radke Dörte, Salomaa Veikko, Willems van Dijk Ko, Boerwinkle Eric, Vasan Ramachandran S, Ferrucci Luigi, Gibson Quince D, Bandinelli Stefania, Snieder Harold, Boomsma Dorret I, Xiao Xiangjun, Campbell Harry, Hayward Caroline, Pramstaller Peter P, van Duijn Cornelia M, Peltonen Leena, Psaty Bruce M, Gudnason Vilmundur, Ridker Paul M, Homuth Georg, Koenig Wolfgang, Ballantyne Christie M, Witteman Jacqueline C M, Benjamin Emelia J, Perola Markus, Chasman Daniel |
Influence of elevated-CRP level-related polymorphisms in non-rheumatic Caucasians on the risk of subclinical atherosclerosis and cardiovascular disease in rheumatoid arthritis. Scientific reports 2016 6 31979. López-Mejías Raquel, Genre Fernanda, Remuzgo-Martínez Sara, González-Juanatey Carlos, Robustillo-Villarino Montserrat, Llorca Javier, Corrales Alfonso, Vicente Esther, Miranda-Filloy José A, Magro César, Tejera-Segura Beatriz, Ramírez Huaranga Marco A, Pina Trinitario, Blanco Ricardo, Alegre-Sancho Juan J, Raya Enrique, Mijares Verónica, Ubilla Begoña, Mínguez Sánchez María D, Gómez-Vaquero Carmen, Balsa Alejandro, Pascual-Salcedo Dora, López-Longo Francisco J, Carreira Patricia, González-Álvaro Isidoro, Rodríguez-Rodríguez Luis, Fernández-Gutiérrez Benjamín, Ferraz-Amaro Iván, Castañeda Santos, Martín Javier, González-Gay Miguel |
Genes involved in angiogenesis and mTOR pathways are frequently mutated in Asian patients with pancreatic neuroendocrine tumors. International journal of biological sciences 2016 12 (12): 1523-1532. Chou Wen-Chi, Lin Po-Han, Yeh Yi-Chen, Shyr Yi-Ming, Fang Wen-Liang, Wang Shin-E, Liu Chun-Yu, Chang Peter Mu-Hsin, Chen Ming-Han, Hung Yi-Ping, Li Chung-Pin, Chao Yee, Chen Ming-Hua |
Genetic susceptibility to pre diabetes mellitus and related association with obesity and physical fitness components in Mexican-Mestizos. Primary care diabetes 2018 Jul . Costa-Urrutia Paula, Abud Carolina, Franco-Trecu Valentina, Colistro Valentina, Rodríguez-Arellano Martha Eunice, Granados Julio, Seelaender Maril |
Clinicopathological and genomic comparisons between different histologic components in combined small cell lung cancer and non-small cell lung cancer. Lung cancer (Amsterdam, Netherlands) 2018 11 125 282-290. Lin Mong-Wei, Su Kang-Yi, Su Te-Jen, Chang Chia-Ching, Lin Jing-Wei, Lee Yi-Hsuan, Yu Sung-Liang, Chen Jin-Shing, Hsieh Min-S |
ASCL1 is a MYCN- and LMO1-dependent member of the adrenergic neuroblastoma core regulatory circuitry. Nature communications 2019 12 10 (1): 5622. Wang Lu, Tan Tze King, Durbin Adam D, Zimmerman Mark W, Abraham Brian J, Tan Shi Hao, Ngoc Phuong Cao Thi, Weichert-Leahey Nina, Akahane Koshi, Lawton Lee N, Rokita Jo Lynne, Maris John M, Young Richard A, Look A Thomas, Sanda Takao |
Polymorphism in ASCL1 target gene DDC is associated with clinical outcomes of small cell lung cancer patients. Thoracic cancer 2019 Nov . Kim Ji Hyun, Lee Shin Yup, Choi Jin Eun, Do Sook Kyung, Lee Jang Hyuck, Hong Mi Jeong, Kang Hyo-Gyoung, Lee Won Kee, Shin Kyung Min, Jeong Ji Yun, Choi Sun Ha, Lee Yong Hoon, Seo Hyewon, Yoo Seung Soo, Lee Jaehee, Cha Seung Ick, Kim Chang Ho, Park Jae Yo |
Differential sensitivity of human neurons carrying ? opioid receptor (MOR) N40D variants in response to ethanol. Alcohol (Fayetteville, N.Y.) 2020 6 87 97-109. Scarnati Matthew S, Boreland Andrew J, Joel Marisa, Hart Ronald P, Pang Zhiping |
Elevation of DNA Methylation in the Promoter Regions of the Brain-Derived Neurotrophic Factor Gene is Associated with Heroin Addiction. Journal of molecular neuroscience : MN 2021 6 71 (9): 1752-1760. Xiao Yifan, Zhu Yongsheng, Li Yunxi |
Further description of two individuals with de novo p.(Glu127Lys) missense variant in the ASCL1 gene. Clinical genetics 2024 1 . Marlène Malbos, Emma Wakeling, Thierry Gautier, Odile Boespflug-Tanguy, Louise Busby, Tashunka Taylor-Miller, Benjamin Dudoignon, Plamen Bokov, Jérôme Govin, Margot Grisval, Adélaïde Rega, Marie-Gabrielle Mourot De Rougemont, Marie-Hélène Aubriot-Lorton, Véronique Darmency, Candace Bensignor, Anne Houzel, Frédéric Huet, Anne-Sophie Denommé-Pichon, Julian Delanne, Frédéric Tran Mau-Them, Ange-Line Bruel, Hana Safraou, Sophie Nambot, Aurore Garde, Christophe Philippe, Yannis Duffourd, Antonio Vitobello, Laurence Faivre, Christel Thauvin-Robin |
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