Artículos de revistas sobre el tema "Association copy"
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Teare, Brian. "from Association Copy". New England Review 43, n.º 3 (2022): 107–13. http://dx.doi.org/10.1353/ner.2022.0089.
Texto completoBrezina, Stefanie, Moritz Feigl, Tanja Gumpenberger, Ricarda Staudinger, Andreas Baierl y Andrea Gsur. "Genome-wide association study of germline copy number variations reveals an association with prostate cancer aggressiveness". Mutagenesis 35, n.º 3 (7 de abril de 2020): 283–90. http://dx.doi.org/10.1093/mutage/geaa010.
Texto completoAi, Zhen, Ming Li, Wenting Liu, Jia-Nee Foo, Omniah Mansouri, Peiran Yin, Qian Zhou et al. "Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction". Science Translational Medicine 8, n.º 345 (29 de junio de 2016): 345ra88. http://dx.doi.org/10.1126/scitranslmed.aaf2106.
Texto completoZHANG, XueGong y XueYa ZHOU. "Copy number variation based genetic association studies". Chinese Science Bulletin 56, n.º 6 (1 de marzo de 2011): 370–82. http://dx.doi.org/10.1360/972010-1759.
Texto completoNygaard, Sune Boris, Maria Unni Rømer, Ib Jarle Christensen, Signe Lykke Nielsen, David Hersi Smith, Kirsten Vang Nielsen, Sven Müller, Ben Vainer, Hans J. Nielsen y Nils Brünner. "TOP1 gene copy number in stage III colorectal cancer (CRC) samples: Association to prognosis." Journal of Clinical Oncology 30, n.º 4_suppl (1 de febrero de 2012): 475. http://dx.doi.org/10.1200/jco.2012.30.4_suppl.475.
Texto completoValla, Marit, Signe Opdahl, Borgny Ytterhus y Anna Mary Bofin. "DTX3 copy number increase in breast cancer: a study of associations to molecular subtype, proliferation and prognosis". Breast Cancer Research and Treatment 187, n.º 1 (22 de febrero de 2021): 57–67. http://dx.doi.org/10.1007/s10549-021-06138-2.
Texto completoWhitman, Mary C., Sherin Shaaban, Sarah MacKinnon, Wai-Man Chan, David A. Mackey, David G. Hunter y Elizabeth C. Engle. "Genetic associations in esotropia: genome-wide association study and copy number variation". Journal of American Association for Pediatric Ophthalmology and Strabismus 23, n.º 4 (agosto de 2019): e63. http://dx.doi.org/10.1016/j.jaapos.2019.08.231.
Texto completoJiang, Rui, Jie Cheng, Xiu-Kai Cao, Yi-Lei Ma, Buren Chaogetu, Yong-Zhen Huang, Xian-Yong Lan, Chu-Zhao Lei, Lin-Yong Hu y Hong Chen. "Copy Number Variation of the SHE Gene in Sheep and Its Association with Economic Traits". Animals 9, n.º 8 (6 de agosto de 2019): 531. http://dx.doi.org/10.3390/ani9080531.
Texto completoLeón-Mimila, Paola, Hugo Villamil-Ramírez, Blanca López-Contreras, Sofía Morán-Ramos, Luis Macias-Kauffer, Víctor Acuña-Alonzo, Blanca del Río-Navarro et al. "Low Salivary Amylase Gene (AMY1) Copy Number Is Associated with Obesity and Gut Prevotella Abundance in Mexican Children and Adults". Nutrients 10, n.º 11 (1 de noviembre de 2018): 1607. http://dx.doi.org/10.3390/nu10111607.
Texto completoVenkatapoorna, Chandra, Priscilla Ayine, Emily Parra, Taylor Koenigs, Megan Phillips, Jeganathan Babu, Maninder Sandey y Thangiah Geetha. "Association of Salivary Amylase (AMY1) Gene Copy Number with Obesity in Alabama Elementary School Children". Nutrients 11, n.º 6 (19 de junio de 2019): 1379. http://dx.doi.org/10.3390/nu11061379.
Texto completoMuir, Scott P. y Sara Dallas. "ALA Committee on Professional Ethics". Journal of Intellectual Freedom and Privacy 1, n.º 2-3 (30 de diciembre de 2016): 13. http://dx.doi.org/10.5860/jifp.v1i2-3.6167.
Texto completoWang, Xiang, Ding Zhang, Guoqiang Wang, Anqi Duan, Xiang Ruan y Teng Zhao. "Association between PD-L1 variants and PD-L1 expression: A pan-cancer analysis." Journal of Clinical Oncology 38, n.º 15_suppl (20 de mayo de 2020): e13661-e13661. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e13661.
Texto completoMcDermott, Mary M., Charlotte A. Peterson, Robert Sufit, Luigi Ferrucci, Jack M. Guralnik, Melina R. Kibbe, Tamar S. Polonsky et al. "Peripheral artery disease, calf skeletal muscle mitochondrial DNA copy number, and functional performance". Vascular Medicine 23, n.º 4 (8 de mayo de 2018): 340–48. http://dx.doi.org/10.1177/1358863x18765667.
Texto completoAslam, M. Muaaz, Peter John, Kang-Hsien Fan, Javaid Mehmood Malik, Eleanor Feingold, F. Yesim Demirci y M. Ilyas Kamboh. "Association of Fc Gamma Receptor 3B Gene Copy Number Variation with Rheumatoid Arthritis Susceptibility". Genes 13, n.º 12 (29 de noviembre de 2022): 2238. http://dx.doi.org/10.3390/genes13122238.
Texto completoLi, Xing, Chenling Qu, Yan Wang, Zhenxing Mao, Chongjian Wang, Wenjie Li y Songcheng Yu. "Associations of CYP24A1 copy number variation with vitamin D deficiency and insulin secretion". Applied Physiology, Nutrition, and Metabolism 44, n.º 12 (diciembre de 2019): 1367–70. http://dx.doi.org/10.1139/apnm-2019-0193.
Texto completoBreheny, Patrick, Prabhakar Chalise, Anthony Batzler, Liewei Wang y Brooke L. Fridley. "Genetic Association Studies of Copy-Number Variation: Should Assignment of Copy Number States Precede Testing?" PLoS ONE 7, n.º 4 (6 de abril de 2012): e34262. http://dx.doi.org/10.1371/journal.pone.0034262.
Texto completoSkuratovskaia, D. A., J. K. Sofronova, P. A. Zatolokin, M. A. Vasilenko, L. S. Litvinova y I. O. Mazunin. "The association of the mitochondrial DNA oriB variants with metabolic syndrome". Biomeditsinskaya Khimiya 63, n.º 6 (2017): 533–38. http://dx.doi.org/10.18097/pbmc20176306533.
Texto completoChen, Rene, Esther Thorson y Stephen Lacy. "The Impact of Newsroom Investment on Newspaper Revenues and Profits: Small and Medium Newspapers, 1998–2002". Journalism & Mass Communication Quarterly 82, n.º 3 (septiembre de 2005): 516–32. http://dx.doi.org/10.1177/107769900508200303.
Texto completoYang, Peng, Zijing Zhang, Jiawei Xu, Kaixing Qu, Shijie Lyv, Xianwei Wang, Cuicui Cai et al. "The Association of the Copy Number Variation of the MLLT10 Gene with Growth Traits of Chinese Cattle". Animals 10, n.º 2 (5 de febrero de 2020): 250. http://dx.doi.org/10.3390/ani10020250.
Texto completoAhumada, Viviana A., Kristen McEachern, Kristy Kuplast-Barr y Kurt Alex Schalper. "Abstract 2508: Clinical significance of PARP7 (TIPARP) gene copy number alterations in human non-small cell and head & neck carcinomas". Cancer Research 83, n.º 7_Supplement (4 de abril de 2023): 2508. http://dx.doi.org/10.1158/1538-7445.am2023-2508.
Texto completoKarimi, Leila, Lies Lahousse, Mohsen Ghanbari, Natalie Terzikhan, André G. Uitterlinden, Johan van der Lei, Guy G. Brusselle, Bruno H. Stricker y Katia M. C. Verhamme. "β2-Adrenergic Receptor (ADRB2) Gene Polymorphisms and Risk of COPD Exacerbations: The Rotterdam Study". Journal of Clinical Medicine 8, n.º 11 (1 de noviembre de 2019): 1835. http://dx.doi.org/10.3390/jcm8111835.
Texto completoSUN, Yu-Lin, Fei LIU y Xiao-Hang ZHAO. "Genome-wide Association Analysis Based on Copy Number Variations*". PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS 36, n.º 8 (16 de octubre de 2009): 968–77. http://dx.doi.org/10.3724/sp.j.1206.2008.00881.
Texto completoLiu, Xue, Ryan J. Longchamps, Kerri L. Wiggins, Laura M. Raffield, Lawrence F. Bielak, Wei Zhao, Achilleas Pitsillides et al. "Association of mitochondrial DNA copy number with cardiometabolic diseases". Cell Genomics 1, n.º 1 (octubre de 2021): 100006. http://dx.doi.org/10.1016/j.xgen.2021.100006.
Texto completoMcCarroll, Steven A. y David M. Altshuler. "Copy-number variation and association studies of human disease". Nature Genetics 39, S7 (27 de junio de 2007): S37—S42. http://dx.doi.org/10.1038/ng2080.
Texto completoMcCarroll, S. A. "Extending genome-wide association studies to copy-number variation". Human Molecular Genetics 17, R2 (15 de octubre de 2008): R135—R142. http://dx.doi.org/10.1093/hmg/ddn282.
Texto completoPlagnol, Vincent. "Association tests and software for copy number variant data". Human Genomics 3, n.º 2 (2009): 191. http://dx.doi.org/10.1186/1479-7364-3-2-191.
Texto completoLin, Peng, Sarah M. Hartz, Jen-Chyong Wang, Robert F. Krueger, Tatiana M. Foroud, Howard J. Edenberg, John I. Nurnberger, Jr et al. "Copy Number Variation Accuracy in Genome-Wide Association Studies". Human Heredity 71, n.º 3 (2011): 141–47. http://dx.doi.org/10.1159/000324683.
Texto completoLee, Jae-Ho y Dae-Kwang Kim. "Association between Mitochondrial D-loop Polymorphism and Copy Number". Korean Journal of Physical Anthropology 27, n.º 3 (2014): 131. http://dx.doi.org/10.11637/kjpa.2014.27.3.131.
Texto completoAshar, Foram N., Yiyi Zhang, Ryan J. Longchamps, John Lane, Anna Moes, Megan L. Grove, Josyf C. Mychaleckyj et al. "Association of Mitochondrial DNA Copy Number With Cardiovascular Disease". JAMA Cardiology 2, n.º 11 (1 de noviembre de 2017): 1247. http://dx.doi.org/10.1001/jamacardio.2017.3683.
Texto completoBaker, William. "King Poppy : An Association Copy: An Addendum to McCormack". Victorian Poetry 61, n.º 1 (marzo de 2023): 129–30. http://dx.doi.org/10.1353/vp.2023.a905524.
Texto completoKumar, Bhupender, Zafar Iqbal Bhat, Savita Bansal, Sunil Saini, Afreen Naseem, Khushnuma Wahabi, Archana Burman, Geeta Trilok Kumar, Sundeep Singh Saluja y M. Moshahid Alam Rizvi. "Association of mitochondrial copy number variation and T16189C polymorphism with colorectal cancer in North Indian population". Tumor Biology 39, n.º 11 (noviembre de 2017): 101042831774029. http://dx.doi.org/10.1177/1010428317740296.
Texto completoWatson, R. G., F. Muhale, L. Thorne, J. Yu, B. O’Neil, J. M. Hoskins, M. O. Myers, H. L. McLeod y J. T. Auman. "Association of copy number variants in colorectal liver metastases with 5-fluorouracil resistance". Journal of Clinical Oncology 27, n.º 15_suppl (20 de mayo de 2009): e14502-e14502. http://dx.doi.org/10.1200/jco.2009.27.15_suppl.e14502.
Texto completoBrucker, Amanda, Wenbin Lu, Rachel Marceau West, Qi-You Yu, Chuhsing Kate Hsiao, Tzu-Hung Hsiao, Ching-Heng Lin et al. "Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis". PLOS Computational Biology 16, n.º 5 (4 de mayo de 2020): e1007797. http://dx.doi.org/10.1371/journal.pcbi.1007797.
Texto completoLi, LiJuan, Peng Yang, ShuYue Shi, ZiJing Zhang, QiaoTing Shi, JiaWei Xu, Hua He et al. "Association Analysis to Copy Number Variation (CNV) of Opn4 Gene with Growth Traits of Goats". Animals 10, n.º 3 (6 de marzo de 2020): 441. http://dx.doi.org/10.3390/ani10030441.
Texto completoCai, Meiying, Na Lin, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Ying Li, Yuan Lin, Hailong Huang y Liangpu Xu. "Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array". Molecular Biology Reports 47, n.º 10 (15 de septiembre de 2020): 7529–35. http://dx.doi.org/10.1007/s11033-020-05815-7.
Texto completoDunstan, Emma, Sue Lester, Rachel Black, Maureen Rischmueller, Helen Chan, Alex W. Hewitt y Catherine L. Hill. "No Association between FCγR3B Copy Number Variation and Susceptibility to Biopsy-Proven Giant Cell Arteritis". Arthritis 2013 (20 de agosto de 2013): 1–4. http://dx.doi.org/10.1155/2013/514914.
Texto completoGolubovic, Milica. "Judicial Professional Associations: Fostering Judicial Reform Through Civil Society Development". Southeastern Europe 33, n.º 1 (2009): 48–62. http://dx.doi.org/10.1163/187633309x421157.
Texto completoWong, Jason Yat-Yang, Richard Cawthon, Wei Hu, Somayina Ezennia, Shahinaz Gadalla, Charles Breeze, Batel Blechter et al. "Abstract 2251: Alu retroelement copy number, leukocyte telomere length, and lung cancer risk in the prospective Prostate, Lung, Colorectal and Ovarian Cancer (PLCO) Screening Trial". Cancer Research 82, n.º 12_Supplement (15 de junio de 2022): 2251. http://dx.doi.org/10.1158/1538-7445.am2022-2251.
Texto completoXiong, Lie, Pei-Fen Kuan, Jianan Tian, Sunduz Keles y Sijian Wang. "Multivariate Boosting for Integrative Analysis of High-Dimensional Cancer Genomic Data". Cancer Informatics 13s7 (enero de 2014): CIN.S16353. http://dx.doi.org/10.4137/cin.s16353.
Texto completoHu, Wei. "Abstract 2255: Alu retroelement copy number alterations and non-Hodgkin lymphoma". Cancer Research 82, n.º 12_Supplement (15 de junio de 2022): 2255. http://dx.doi.org/10.1158/1538-7445.am2022-2255.
Texto completoGu, Wenjuan, Hyungwon Choi y Debashis Ghosh. "Global Associations between Copy Number and Transcript mRNA Microarray Data: An Empirical Study". Cancer Informatics 6 (enero de 2008): CIN.S342. http://dx.doi.org/10.4137/cin.s342.
Texto completoHuang, Liansha, Dacai Teng, Hao Wang, Guoqing Sheng y Tonghua Liu. "Association of copy number variation in the AHI1 gene with risk of obesity in the Chinese population". European Journal of Endocrinology 166, n.º 4 (abril de 2012): 727–34. http://dx.doi.org/10.1530/eje-11-0999.
Texto completoLanktree, M. y R. A. Hegele. "COPY NUMBER VARIATION IN METABOLIC SYNDROME". Clinical & Investigative Medicine 31, n.º 4 (1 de agosto de 2008): 15. http://dx.doi.org/10.25011/cim.v31i4.4812.
Texto completoGlessner, Joseph T., Jin Li y Hakon Hakonarson. "ParseCNV integrative copy number variation association software with quality tracking". Nucleic Acids Research 41, n.º 5 (3 de enero de 2013): e64-e64. http://dx.doi.org/10.1093/nar/gks1346.
Texto completoLi, Man, Jacob Carey, Stephen Cristiano, Katalin Susztak, Josef Coresh, Eric Boerwinkle, Wen Hong L. Kao, Terri H. Beaty, Anna Köttgen y Robert B. Scharpf. "Genome-Wide Association of Copy Number Polymorphisms and Kidney Function". PLOS ONE 12, n.º 1 (30 de enero de 2017): e0170815. http://dx.doi.org/10.1371/journal.pone.0170815.
Texto completoSebat, J., B. Lakshmi, D. Malhotra, J. Troge, C. Lese-Martin, T. Walsh, B. Yamrom et al. "Strong Association of De Novo Copy Number Mutations with Autism". Science 316, n.º 5823 (20 de abril de 2007): 445–49. http://dx.doi.org/10.1126/science.1138659.
Texto completoBentley, Robert W., John Pearson, Richard B. Gearry, Murray L. Barclay, Cushla McKinney, Tony R. Merriman y Rebecca L. Roberts. "Association of Higher DEFB4 Genomic Copy Number With Crohnʼs Disease". American Journal of Gastroenterology 105, n.º 2 (febrero de 2010): 354–59. http://dx.doi.org/10.1038/ajg.2009.582.
Texto completoEleftherohorinou, H., J. C. Andersson-Assarsson, R. G. Walters, J. S. El-Sayed Moustafa, L. Coin, P. Jacobson, L. M. S. Carlsson et al. "famCNV: copy number variant association for quantitative traits in families". Bioinformatics 27, n.º 13 (5 de mayo de 2011): 1873–75. http://dx.doi.org/10.1093/bioinformatics/btr264.
Texto completoSerrano, Nicholas Anthony, Chang Xu, John Houck, Pei Wang, Wenhong Fan, Yan Liu y Pawadee Lohavanichbutr. "Association of DNA Copy Number and miRNA Expression in OSCC". Otolaryngology–Head and Neck Surgery 145, n.º 2_suppl (agosto de 2011): P60. http://dx.doi.org/10.1177/0194599811416318a63.
Texto completoThyagarajan, Bharat, Weihua Guan, Veronika Fedirko, Helene Barcelo, Huakang Tu, Myron Gross, Michael Goodman y Roberd M. Bostick. "No association between mitochondrial DNA copy number and colorectal adenomas". Molecular Carcinogenesis 55, n.º 8 (10 de agosto de 2015): 1290–96. http://dx.doi.org/10.1002/mc.22370.
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