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Single Nucleotide Polymorphisms in Noncoding Regions of Rad51C Do Not Change the Risk of Unselected Breast Cancer but They Modulate the Level of Oxidative Stress and the DNA Damage Characteristics: A Case-Control Study
Gresner, Peter, Gromadzinska, Jolanta, Jablonska, Ewa, Stepnik, Maciej, Zambrano Quispe, Oscar, Twardowska, Ewa, Wasowicz, Wojciech
Published in PloS one (24.10.2014)
Published in PloS one (24.10.2014)
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Single Nucleotide Polymorphisms in Noncoding Regions of Rad51C Do Not Change the Risk of Unselected Breast Cancer but They Modulate the Level of Oxidative Stress and the DNA Damage Characteristics: A Case-Control Study: e110696
Gresner, Peter, Gromadzinska, Jolanta, Jablonska, Ewa, Stepnik, Maciej, Quispe, Oscar Zambrano, Twardowska, Ewa, Wasowicz, Wojciech
Published in PloS one (01.10.2014)
Published in PloS one (01.10.2014)
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Divergent contributions of coding and noncoding sequences to initial high‐altitude adaptation in passerine birds endemic to the Qinghai–Tibet Plateau
Hao, Yan, Song, Gang, Zhang, Yong E., Zhai, Weiwei, Jia, Chenxi, Ji, Yanzhu, Tang, Shiyu, Lv, Hongrui, Qu, Yanhua, Lei, Fumin
Published in Molecular ecology (01.07.2023)
Published in Molecular ecology (01.07.2023)
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Primary familial brain calcification linked to deletion of 5’ noncoding region of SLC20A2
Pasanen, P., Mäkinen, J., Myllykangas, L., Guerreiro, R., Bras, J., Valori, M., Viitanen, M., Baumann, M., Tienari, P. J., Pöyhönen, M., Baumann, P.
Published in Acta neurologica Scandinavica (01.07.2017)
Published in Acta neurologica Scandinavica (01.07.2017)
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Influence of the genetic polymorphism in the 5′-noncoding region of the CYP1A2 gene on CYP1A2 phenotype and urinary mutagenicity in smokers
Pavanello, Sofia, Pulliero, Alessandra, Lupi, Silvia, Gregorio, Pasquale, Clonfero, Erminio
Published in Mutation research (10.11.2005)
Published in Mutation research (10.11.2005)
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Abstract 200: Functional Mapping of the 8q24 Noncoding Region Reveals Enhancer Elements and Association Between GWAS SNPs and TRIB1 Gene Expression
Berrido, Andrea M, Smith, Mikhaila A, Hand, Nicholas J, Brown, Christopher D, Rader, Daniel J, Bauer, Robert C
Published in Arteriosclerosis, thrombosis, and vascular biology (01.05.2017)
Published in Arteriosclerosis, thrombosis, and vascular biology (01.05.2017)
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Predicting gene expression in massively parallel reporter assays: A comparative study
Kreimer, Anat, Zeng, Haoyang, Edwards, Matthew D., Guo, Yuchun, Tian, Kevin, Shin, Sunyoung, Welch, Rene, Wainberg, Michael, Mohan, Rahul, Sinnott‐Armstrong, Nicholas A., Li, Yue, Eraslan, Gökcen, AMIN, Talal Bin, Tewhey, Ryan, Sabeti, Pardis C., Goke, Jonathan, Mueller, Nikola S., Kellis, Manolis, Kundaje, Anshul, Beer, Michael A, Keles, Sunduz, Gifford, David K., Yosef, Nir
Published in Human mutation (01.09.2017)
Published in Human mutation (01.09.2017)
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Human Lung DNA Methylation Quantitative Trait Loci Colocalize with Chronic Obstructive Pulmonary Disease Genome-Wide Association Loci
Morrow, Jarrett D., Glass, Kimberly, Cho, Michael H., Hersh, Craig P., Pinto-Plata, Victor, Celli, Bartolome, Marchetti, Nathaniel, Criner, Gerard, Bueno, Raphael, Washko, George, Choi, Augustine M. K., Quackenbush, John, Silverman, Edwin K., DeMeo, Dawn L.
Published in American journal of respiratory and critical care medicine (15.05.2018)
Published in American journal of respiratory and critical care medicine (15.05.2018)
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Assessment of 2q23.1 Microdeletion Syndrome Implicates MBD5 as a Single Causal Locus of Intellectual Disability, Epilepsy, and Autism Spectrum Disorder
Talkowski, Michael E., Mullegama, Sureni V., Rosenfeld, Jill A., van Bon, Bregje W.M., Shen, Yiping, Repnikova, Elena A., Gastier-Foster, Julie, Thrush, Devon Lamb, Kathiresan, Sekar, Ruderfer, Douglas M., Chiang, Colby, Hanscom, Carrie, Ernst, Carl, Lindgren, Amelia M., Morton, Cynthia C., An, Yu, Astbury, Caroline, Brueton, Louise A., Lichtenbelt, Klaske D., Ades, Lesley C., Fichera, Marco, Romano, Corrado, Innis, Jeffrey W., Williams, Charles A., Bartholomew, Dennis, Van Allen, Margot I., Parikh, Aditi, Zhang, Lilei, Wu, Bai-Lin, Pyatt, Robert E., Schwartz, Stuart, Shaffer, Lisa G., de Vries, Bert B.A., Gusella, James F., Elsea, Sarah H.
Published in American journal of human genetics (07.10.2011)
Published in American journal of human genetics (07.10.2011)
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Paternally inherited cis-regulatory structural variants are associated with autism
Brandler, William M., Antaki, Danny, Gujral, Madhusudan, Kleiber, Morgan L., Whitney, Joe, Maile, Michelle S., Hong, Oanh, Chapman, Timothy R., Tan, Shirley, Tandon, Prateek, Pang, Timothy, Tang, Shih C., Vaux, Keith K., Yang, Yan, Harrington, Eoghan, Juul, Sissel, Turner, Daniel J., Thiruvahindrapuram, Bhooma, Kaur, Gaganjot, Wang, Zhuozhi, Kingsmore, Stephen F., Gleeson, Joseph G., Bisson, Denis, Kakaradov, Boyko, Telenti, Amalio, Venter, J. Craig, Corominas, Roser, Toma, Claudio, Cormand, Bru, Rueda, Isabel, Guijarro, Silvina, Messer, Karen S., Nievergelt, Caroline M., Arranz, Maria J., Courchesne, Eric, Pierce, Karen, Muotri, Alysson R., Iakoucheva, Lilia M., Hervas, Amaia, Scherer, Stephen W., Corsello, Christina, Sebat, Jonathan
Published in Science (American Association for the Advancement of Science) (20.04.2018)
Published in Science (American Association for the Advancement of Science) (20.04.2018)
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Evolutionary dynamics of recent selection on cognitive abilities
Miller, Sara E., Legan, Andrew W., Henshaw, Michael T., Ostevik, Katherine L., Samuk, Kieran, Uy, Floria M. K., Sheehan, Michael J.
Published in Proceedings of the National Academy of Sciences - PNAS (11.02.2020)
Published in Proceedings of the National Academy of Sciences - PNAS (11.02.2020)
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LINC01149 variant modulates MICA expression that facilitates hepatitis B virus spontaneous recovery but increases hepatocellular carcinoma risk
Zhong, Rong, Tian, Jianbo, Fu, Mingpeng, Ma, Simin, Liu, Li, Li, Jiaoyuan, Shen, Na, Ke, Juntao, Yang, Yang, Gong, Yajie, Zhu, Ying, Wang, Ying, Gong, Jing, Chang, Jiang, Lei, Ping, Cheng, Xiang, Huang, Kun, Shen, Guanxin, Miao, Xiaoping
Published in Oncogene (01.02.2020)
Published in Oncogene (01.02.2020)
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Gene variants of the SLC2A5 gene encoding GLUT5, the major fructose transporter, do not contribute to clinical presentation of acquired fructose malabsorption
Taneva, Irina, Grumann, Dorothee, Schmidt, Dietmar, Taneva, Elina, von Arnim, Ulrike, Ansorge, Thomas, Wex, Thomas
Published in BMC gastroenterology (06.04.2022)
Published in BMC gastroenterology (06.04.2022)
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