Artículos de revistas sobre el tema "Non coding variations"
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Pan, Qi, Yue-Juan Liu, Xue-Feng Bai, Xiao-Le Han, Yong Jiang, Bo Ai, Shan-Shan Shi et al. "VARAdb: a comprehensive variation annotation database for human". Nucleic Acids Research 49, n.º D1 (23 de octubre de 2020): D1431—D1444. http://dx.doi.org/10.1093/nar/gkaa922.
Texto completoLaurent, Jon M., Sudarshan Pinglay, Leslie Mitchell y Ran Brosh. "Probing the dark matter of the human genome with big DNA". Biochemist 41, n.º 3 (1 de junio de 2019): 46–48. http://dx.doi.org/10.1042/bio04103046.
Texto completoSedláková, V., P. Sedlák, D. Zeka, J. Domkářová, P. Doležal y P. Vejl. "Evaluation of variations in plastid DNA non-coding regions in selected species of the genus Solanum". Czech Journal of Genetics and Plant Breeding 53, No. 3 (13 de septiembre de 2017): 127–31. http://dx.doi.org/10.17221/76/2015-cjgpb.
Texto completoMeerschaut, Ilse, Sarah Vergult, Annelies Dheedene, Björn Menten, Katya De Groote, Hans De Wilde, Laura Muiño Mosquera et al. "A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome". Genes 12, n.º 7 (8 de julio de 2021): 1048. http://dx.doi.org/10.3390/genes12071048.
Texto completoBhartiya, Deeksha y Vinod Scaria. "Genomic variations in non-coding RNAs: Structure, function and regulation". Genomics 107, n.º 2-3 (marzo de 2016): 59–68. http://dx.doi.org/10.1016/j.ygeno.2016.01.005.
Texto completoBozgeyik, Esra y Ibrahim Bozgeyik. "Non-coding RNA variations in oral cancers: A comprehensive review". Gene 851 (enero de 2023): 147012. http://dx.doi.org/10.1016/j.gene.2022.147012.
Texto completoScarpa, Aldo y Andrea Mafficini. "Non-coding regulatory variations: the dark matter of pancreatic cancer genomics". Gut 67, n.º 3 (28 de junio de 2017): 399–400. http://dx.doi.org/10.1136/gutjnl-2017-314310.
Texto completoHaas, Jan, Stefan Mester, Alan Lai, Karen S. Frese, Farbod Sedaghat‐Hamedani, Elham Kayvanpour, Tobias Rausch et al. "Genomic structural variations lead to dysregulation of important coding and non‐coding RNA species in dilated cardiomyopathy". EMBO Molecular Medicine 10, n.º 1 (14 de noviembre de 2017): 107–20. http://dx.doi.org/10.15252/emmm.201707838.
Texto completoSedano, Melina J., Alana L. Harrison, Mina Zilaie, Chandrima Das, Ramesh Choudhari, Enrique Ramos y Shrikanth S. Gadad. "Emerging Roles of Estrogen-Regulated Enhancer and Long Non-Coding RNAs". International Journal of Molecular Sciences 21, n.º 10 (25 de mayo de 2020): 3711. http://dx.doi.org/10.3390/ijms21103711.
Texto completoMattick, John S. "The central role of RNA in the genetic programming of complex organisms". Anais da Academia Brasileira de Ciências 82, n.º 4 (diciembre de 2010): 933–39. http://dx.doi.org/10.1590/s0001-37652010000400016.
Texto completoKim, Eun Jin, Hyun Jin Yu y Dong Wook Kim. "Sequence Variations in the Non-Coding Sequence of CTX Phages in Vibrio cholerae". Journal of Microbiology and Biotechnology 26, n.º 8 (28 de agosto de 2016): 1473–80. http://dx.doi.org/10.4014/jmb.1604.04022.
Texto completoLabani, Mahdieh, Amin Beheshti, Ahmadreza Argha y Hamid Alinejad-Rokny. "A Comprehensive Investigation of Genomic Variants in Prostate Cancer Reveals 30 Putative Regulatory Variants". International Journal of Molecular Sciences 24, n.º 3 (27 de enero de 2023): 2472. http://dx.doi.org/10.3390/ijms24032472.
Texto completoTsilimigras, Diamantis I., Sofia-Iris Bibli, Gerasimos Siasos, Evangelos Oikonomou, Despina N. Perrea, Konstantinos Filis, Dimitrios Tousoulis y Fragiska Sigala. "Regulation of Long Non-Coding RNAs by Statins in Atherosclerosis". Biomolecules 11, n.º 5 (22 de abril de 2021): 623. http://dx.doi.org/10.3390/biom11050623.
Texto completoYasmin, Tahirah. "In silico comprehensive analysis of coding and non-coding SNPs in human mTOR protein". PLOS ONE 17, n.º 7 (5 de julio de 2022): e0270919. http://dx.doi.org/10.1371/journal.pone.0270919.
Texto completoLange, Marios, Rodiola Begolli y Antonis Giakountis. "Non-Coding Variants in Cancer: Mechanistic Insights and Clinical Potential for Personalized Medicine". Non-Coding RNA 7, n.º 3 (2 de agosto de 2021): 47. http://dx.doi.org/10.3390/ncrna7030047.
Texto completoYarahmadi, Elham, Parnaz Borjian Boroujeni, Mehdi Totonchi y Hamid Gourabi. "Genotyping of the EIF1AY Gene in Iranian Patients with Non-Obstructive Azoospermia". Current Urology 13, n.º 1 (2019): 46–50. http://dx.doi.org/10.1159/000499295.
Texto completoWilson, Claire y Aditi Kanhere. "8q24.21 Locus: A Paradigm to Link Non-Coding RNAs, Genome Polymorphisms and Cancer". International Journal of Molecular Sciences 22, n.º 3 (22 de enero de 2021): 1094. http://dx.doi.org/10.3390/ijms22031094.
Texto completoAllen, Ethan J. y Roberta K. Weber. "An Exploration of Indexed and Non-Indexed Open Access Journals: Identifying Metadata Coding Variations". Journal of Web Librarianship 9, n.º 2-3 (3 de julio de 2015): 65–84. http://dx.doi.org/10.1080/19322909.2015.1020185.
Texto completoTorgersen, H., T. Skern y D. Blaas. "Typing of Human Rhinoviruses Based on Sequence Variations in the 5' Non-coding Region". Journal of General Virology 70, n.º 11 (1 de noviembre de 1989): 3111–16. http://dx.doi.org/10.1099/0022-1317-70-11-3111.
Texto completoWilliams, Sarah M., Joon Yong An, Janette Edson, Michelle Watts, Valentine Murigneux, Andrew J. O. Whitehouse, Colin J. Jackson, Mark A. Bellgrove, Alexandre S. Cristino y Charles Claudianos. "An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder". Molecular Psychiatry 24, n.º 11 (27 de abril de 2018): 1707–19. http://dx.doi.org/10.1038/s41380-018-0049-x.
Texto completoUvarova, Aksinya N., Elena A. Tkachenko, Ekaterina M. Stasevich, Elina A. Zheremyan, Kirill V. Korneev y Dmitry V. Kuprash. "Methods for Functional Characterization of Genetic Polymorphisms of Non-Coding Regulatory Regions of the Human Genome". Biochemistry (Moscow) 89, n.º 6 (junio de 2024): 1002–13. http://dx.doi.org/10.1134/s0006297924060026.
Texto completoBegum, Ghausia, Ammar Albanna, Asma Bankapur, Nasna Nassir, Richa Tambi, Bakhrom K. Berdiev, Hosneara Akter et al. "Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome". International Journal of Molecular Sciences 22, n.º 4 (19 de febrero de 2021): 2060. http://dx.doi.org/10.3390/ijms22042060.
Texto completoProdan-Bărbulescu, Cătălin, Edward Paul Şeclăman, Virgil Enătescu, Ionuţ Flaviu Faur, Laura Andreea Ghenciu, Paul Tuţac, Paul Paşca y Laura Octavia Grigoriţă. "Evaluating the Connection between MicroRNAs and Long Non-Coding RNAs for the Establishment of the Major Depressive Disorder Diagnosis". Biomedicines 12, n.º 3 (25 de febrero de 2024): 516. http://dx.doi.org/10.3390/biomedicines12030516.
Texto completoOlufunmilayo, Edward O. y R. M. Damian Holsinger. "Roles of Non-Coding RNA in Alzheimer’s Disease Pathophysiology". International Journal of Molecular Sciences 24, n.º 15 (6 de agosto de 2023): 12498. http://dx.doi.org/10.3390/ijms241512498.
Texto completoTan, Fengxiao, Weixi Li, Hui Feng, Yelin Huang y Achyut Kumar Banerjee. "Interspecific variation and phylogenetic relationship between mangrove and non-mangrove species of a same family (Meliaceae)—insights from comparative analysis of complete chloroplast genome". PeerJ 11 (26 de junio de 2023): e15527. http://dx.doi.org/10.7717/peerj.15527.
Texto completoChawla, Anjali, Corina Nagy y Gustavo Turecki. "Chromatin Profiling Techniques: Exploring the Chromatin Environment and Its Contributions to Complex Traits". International Journal of Molecular Sciences 22, n.º 14 (16 de julio de 2021): 7612. http://dx.doi.org/10.3390/ijms22147612.
Texto completoShapiro, James A. "Biological action in Read–Write genome evolution". Interface Focus 7, n.º 5 (18 de agosto de 2017): 20160115. http://dx.doi.org/10.1098/rsfs.2016.0115.
Texto completoCao, Ting, ShuangYang Zhang, Qian Chen, CuiRong Zeng, LiWei Wang, ShiMeng Jiao, Hui Chen, BiKui Zhang y HuaLin Cai. "Long non-coding RNAs in schizophrenia: Genetic variations, treatment markers and potential targeted signaling pathways". Schizophrenia Research 260 (octubre de 2023): 12–22. http://dx.doi.org/10.1016/j.schres.2023.07.027.
Texto completoPinjou Tsai, Becky, Liang Li, Min Li, Patrick Halliday, Anastasia Rosales, Stephen J. Forman, Smita Bhatia y Ravi Bhatia. "Development Of t-MDS In Patients Undergoing Autologous Transplantation For Lymphoma Is Not Associated With Increased Frequency Of Mitochondrial DNA Mutations". Blood 122, n.º 21 (15 de noviembre de 2013): 1535. http://dx.doi.org/10.1182/blood.v122.21.1535.1535.
Texto completoPolicarpo, Rafaela y Constantin d’Ydewalle. "Missing lnc(RNAs) in Alzheimer’s Disease?" Genes 13, n.º 1 (23 de diciembre de 2021): 39. http://dx.doi.org/10.3390/genes13010039.
Texto completoCalin, George A. "Abstract IA025: About motifs, non-codingRNAs and metastases". Cancer Research 83, n.º 2_Supplement_2 (15 de enero de 2023): IA025. http://dx.doi.org/10.1158/1538-7445.metastasis22-ia025.
Texto completoHuo, Yan, Han Yang, Wenjie Ding, Zhaohe Yuan y Zunling Zhu. "Exploring the Relationship between Genomic Variation and Phenotype in Ornamental Pomegranate: A Study of Single and Double-Petal Varieties". Horticulturae 9, n.º 3 (9 de marzo de 2023): 361. http://dx.doi.org/10.3390/horticulturae9030361.
Texto completoEl-Hageen, Hazem M., Aadel M. Alatwi y Ahmed Nabih Zaki Rashed. "Advanced modulation coding schemes for an optical transceiver systems–based OWC communication channel model". Bulletin of Electrical Engineering and Informatics 10, n.º 2 (1 de abril de 2021): 767–75. http://dx.doi.org/10.11591/eei.v10i2.2433.
Texto completoBui, Linh T., Heini M. Natri, Lance M. Peter, Bianca Argente, Austin J. Gutierrez, Arnold Federico, Mei-I. Chung, Jonathan Keats y Nicholas E. Banovich. "Abstract 5780: Functions of genetic variation on gene expression and survival in multiple myeloma". Cancer Research 82, n.º 12_Supplement (15 de junio de 2022): 5780. http://dx.doi.org/10.1158/1538-7445.am2022-5780.
Texto completoSu, Yi, Xi Yang, Hai Yi, Fangyi Fan, Haoping Sun, Sihan Lai y Ting Niu. "Identification and Characterization of EBV Genome in NKT Cell Lymphoma". Blood 132, Supplement 1 (29 de noviembre de 2018): 5304. http://dx.doi.org/10.1182/blood-2018-99-118710.
Texto completoHong, Thanh Phuoc y Ling Guan. "A Scale and Rotational Invariant Key-point Detector based on Sparse Coding". ACM Transactions on Intelligent Systems and Technology 12, n.º 3 (11 de junio de 2021): 1–19. http://dx.doi.org/10.1145/3452009.
Texto completoALKANLI, Nevra y Arzu AY. "Kanser Gelişimi ve Progresyonunda miRNA’LAR VE miRNA Gen Varyasyonları". Gevher Nesibe Journal IESDR 6, n.º 13 (25 de julio de 2021): 38–45. http://dx.doi.org/10.46648/gnj.226.
Texto completoTang, Jianmin, Rong Zou, Taiguo Chen, Lipo Pan, Shujing Zhu, Tao Ding, Shengfeng Chai y Xiao Wei. "Comparative Analysis of the Complete Chloroplast Genomes of Six Endangered Cycas Species: Genomic Features, Comparative Analysis, and Phylogenetic Implications". Forests 14, n.º 10 (16 de octubre de 2023): 2069. http://dx.doi.org/10.3390/f14102069.
Texto completoMoutsopoulos, Ilias, Lukas Maischak, Elze Lauzikaite, Sergio A. Vasquez Urbina, Eleanor C. Williams, Hajk-Georg Drost y Irina I. Mohorianu. "noisyR: enhancing biological signal in sequencing datasets by characterizing random technical noise". Nucleic Acids Research 49, n.º 14 (2 de junio de 2021): e83-e83. http://dx.doi.org/10.1093/nar/gkab433.
Texto completoBaumgart, Simon J., Ekaterina Nevedomskaya y Bernard Haendler. "Dysregulated Transcriptional Control in Prostate Cancer". International Journal of Molecular Sciences 20, n.º 12 (13 de junio de 2019): 2883. http://dx.doi.org/10.3390/ijms20122883.
Texto completoHawkins, Gregory A., David J. Friedman, Lingyi Lu, David R. McWilliams, Jeff W. Chou, Satria Sajuthi, Jasmin Divers et al. "Re-Sequencing of the APOL1-APOL4 and MYH9 Gene Regions in African Americans Does Not Identify Additional Risks for CKD Progression". American Journal of Nephrology 42, n.º 2 (2015): 99–106. http://dx.doi.org/10.1159/000439448.
Texto completoOuedraogo, Zangbéwendé Guy, Caroline Janel, Alexandre Janin, Gilles Millat, Sarah Langlais, Bénédicte Pontier, Marie Biard et al. "Relevance of Extending FGFR3 Gene Analysis in Osteochondrodysplasia to Non-Coding Sequences: A Case Report". Genes 15, n.º 2 (10 de febrero de 2024): 225. http://dx.doi.org/10.3390/genes15020225.
Texto completoNorman, Jane E., Matthew L. Jones, Neil V. Morgan, Jacqui Stockley, Martina E. Daly, Stuart J. Mundell, Steve P. Watson y Andrew D. Mumford. "Functional Variations In Genes Encoding Platelet G-Protein Coupled Receptors In Unselected and Platelet Function Disorder Populations". Blood 122, n.º 21 (15 de noviembre de 2013): 3511. http://dx.doi.org/10.1182/blood.v122.21.3511.3511.
Texto completoZorc, Minja y Tanja Kunej. "In silico screening of the chicken genome for overlaps between genomic regions: microRNA genes, coding and non-coding transcriptional units, QTL, and genetic variations". Chromosome Research 24, n.º 2 (22 de enero de 2016): 225–30. http://dx.doi.org/10.1007/s10577-016-9517-9.
Texto completoAmirkhah, Raheleh, Hojjat Naderi-Meshkin, Jaynish Shah, Philip Dunne y Ulf Schmitz. "The Intricate Interplay between Epigenetic Events, Alternative Splicing and Noncoding RNA Deregulation in Colorectal Cancer". Cells 8, n.º 8 (19 de agosto de 2019): 929. http://dx.doi.org/10.3390/cells8080929.
Texto completoAdriaanse, Fabienne R. S., Sadie M. Sakurada, Shondra M. Pruett-Miller, Ronald W. Stam, Michel C. Zwaan y Tanja A. Gruber. "Non-Coding HOX Fusions in Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia". Blood 134, Supplement_1 (13 de noviembre de 2019): 533. http://dx.doi.org/10.1182/blood-2019-127014.
Texto completoUmlauf, David, Peter Fraser y Takashi Nagano. "The role of long non-coding RNAs in chromatin structure and gene regulation: variations on a theme". Biological Chemistry 389, n.º 4 (1 de abril de 2008): 323–31. http://dx.doi.org/10.1515/bc.2008.047.
Texto completoKin, Katherine, Xi Chen, Manuel Gonzalez-Garay y Walid D. Fakhouri. "The effect of non-coding DNA variations on P53 and cMYC competitive inhibition at cis-overlapping motifs". Human Molecular Genetics 25, n.º 8 (7 de febrero de 2016): 1517–27. http://dx.doi.org/10.1093/hmg/ddw030.
Texto completoLezirovitz, Karina, Gleiciele A. Vieira-Silva, Ana C. Batissoco, Débora Levy, Joao P. Kitajima, Alix Trouillet, Ellen Ouyang et al. "A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58". Human Molecular Genetics 29, n.º 9 (27 de abril de 2020): 1520–36. http://dx.doi.org/10.1093/hmg/ddaa075.
Texto completoRischewski, Johannes R., Johanna Wyss, Sylvie Stocker, Martin Hergersberg, Andreas R. Huber y Thomas Kühne. "Rare SOX13 Sequence Variations in Pediatric Idiopathic Thrombocytopenic Purpura Patients." Blood 112, n.º 11 (16 de noviembre de 2008): 3420. http://dx.doi.org/10.1182/blood.v112.11.3420.3420.
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