Artículos de revistas sobre el tema "Mutation"
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GARCÍA-DORADO, A., C. LÓPEZ-FANJUL y A. CABALLERO. "Properties of spontaneous mutations affecting quantitative traits". Genetical Research 74, n.º 3 (diciembre de 1999): 341–50. http://dx.doi.org/10.1017/s0016672399004206.
Texto completoEllis, Nathan A. "Mutation-causing mutations". Nature 381, n.º 6578 (mayo de 1996): 110–11. http://dx.doi.org/10.1038/381110a0.
Texto completoMatsutani, Taro, Yuki Ueno, Tsukasa Fukunaga y Michiaki Hamada. "Discovering novel mutation signatures by latent Dirichlet allocation with variational Bayes inference". Bioinformatics 35, n.º 22 (16 de abril de 2019): 4543–52. http://dx.doi.org/10.1093/bioinformatics/btz266.
Texto completoLee, Joon-Hyop, Jiyoung Ahn, Won Seo Park, Eun Kyung Choe, Eunyoung Kim, Rumi Shin, Seung Chul Heo et al. "Colorectal Cancer Prognosis is Not Associated with BRAF and KRAS Mutations-A STROBE Compliant Study". Journal of Clinical Medicine 8, n.º 1 (17 de enero de 2019): 111. http://dx.doi.org/10.3390/jcm8010111.
Texto completoBustamante, A. V., A. M. Sanso, D. O. Segura, A. E. Parma y P. M. A. Lucchesi. "Dynamic of Mutational Events in Variable Number Tandem Repeats ofEscherichia coliO157:H7". BioMed Research International 2013 (2013): 1–9. http://dx.doi.org/10.1155/2013/390354.
Texto completoPawlik, Timothy M., Darrell R. Borger, Yuhree Kim, David Cosgrove, Sorin Alexandrescu, Ryan Thomas Groeschl, Vikram Deshpande et al. "Genomic profiling of intrahepatic cholangiocarcinoma: Refining prognostic determinants and identifying therapeutic targets." Journal of Clinical Oncology 32, n.º 3_suppl (20 de enero de 2014): 210. http://dx.doi.org/10.1200/jco.2014.32.3_suppl.210.
Texto completoRobinson, Philip S., Tim H. H. Coorens, Claire Palles, Emily Mitchell, Federico Abascal, Sigurgeir Olafsson, Bernard C. H. Lee et al. "Increased somatic mutation burdens in normal human cells due to defective DNA polymerases". Nature Genetics 53, n.º 10 (30 de septiembre de 2021): 1434–42. http://dx.doi.org/10.1038/s41588-021-00930-y.
Texto completoTrindade, Sandra, Lilia Perfeito y Isabel Gordo. "Rate and effects of spontaneous mutations that affect fitness in mutator Escherichia coli". Philosophical Transactions of the Royal Society B: Biological Sciences 365, n.º 1544 (27 de abril de 2010): 1177–86. http://dx.doi.org/10.1098/rstb.2009.0287.
Texto completoWatters, M. K. y D. R. Stadler. "Spontaneous mutation during the sexual cycle of Neurospora crassa." Genetics 139, n.º 1 (1 de enero de 1995): 137–45. http://dx.doi.org/10.1093/genetics/139.1.137.
Texto completoLee, Seung-Shin, Jae-Sook Ahn, Taehyung Kim, Hyeoung Joon Kim, Yeo-Kyeoung Kim, Seo-Yeon Ahn, Sung-Hoon Jung et al. "RUNX1 Mutation in Cytogenetically Normal Acute Myeloid Leukemia : Clinical Implications, Co-Mutation Analysis". Blood 128, n.º 22 (2 de diciembre de 2016): 5253. http://dx.doi.org/10.1182/blood.v128.22.5253.5253.
Texto completoWayne, Marta L. y Trudy F. C. Mackay. "Quantitative Genetics of Ovariole Number in Drosophila melanogaster. II. Mutational Variation and Genotype-Environment Interaction". Genetics 148, n.º 1 (1 de enero de 1998): 201–10. http://dx.doi.org/10.1093/genetics/148.1.201.
Texto completoPálinkás, Hajnalka Laura, Lőrinc Pongor, Máté Balajti, Ádám Nagy, Kinga Nagy, Angéla Békési, Giampaolo Bianchini, Beáta G. Vértessy y Balázs Győrffy. "Primary Founder Mutations in the PRKDC Gene Increase Tumor Mutation Load in Colorectal Cancer". International Journal of Molecular Sciences 23, n.º 2 (6 de enero de 2022): 633. http://dx.doi.org/10.3390/ijms23020633.
Texto completoTarlock, Katherine, Todd M. Cooper, Todd A. Alonzo, Robert Gerbing, Jessica Pollard, Richard Aplenc, E. Anders Kolb, Alan S. Gamis y Soheil Meshinchi. "Mutational Concordance from Diagnosis and Relapse in Pediatric Acute Myeloid Leukemia: A Report from the Children's Oncology Group". Blood 128, n.º 22 (2 de diciembre de 2016): 2846. http://dx.doi.org/10.1182/blood.v128.22.2846.2846.
Texto completoShang, Yanhong, Hao Zhang, Aiming Zang, Shaohua Yuan, Xiaofang Li, Wenpan Zhang, Ran Huo et al. "Abstract 5754: The molecular characteristics of EGFR co-mutations in lung adenocarcinoma". Cancer Research 82, n.º 12_Supplement (15 de junio de 2022): 5754. http://dx.doi.org/10.1158/1538-7445.am2022-5754.
Texto completoKapoor, Ritika R., Sarah E. Flanagan, Piers Fulton, Anupam Chakrapani, Bernadette Chadefaux, Tawfeg Ben-Omran, Indraneel Banerjee, Julian P. Shield, Sian Ellard y Khalid Hussain. "Hyperinsulinism–hyperammonaemia syndrome: novel mutations in the GLUD1 gene and genotype–phenotype correlations". European Journal of Endocrinology 161, n.º 5 (noviembre de 2009): 731–35. http://dx.doi.org/10.1530/eje-09-0615.
Texto completoBalamurugan, Kuppareddi, Martin L. Tracey, Uwe Heine, George C. Maha y George T. Duncan. "Mutation at the Human D1S80 Minisatellite Locus". Scientific World Journal 2012 (2012): 1–8. http://dx.doi.org/10.1100/2012/917235.
Texto completoClaes, Kathleen, Eva Machackova, Michel De Vos, Bruce Poppe, Anne De Paepe y Ludwine Messiaen. "Mutation Analysis of the BRCA1 and BRCA2 Genes in the Belgian Patient Population and Identification of a Belgian Founder Mutation BRCA1 IVS5+3A>G". Disease Markers 15, n.º 1-3 (1999): 69–73. http://dx.doi.org/10.1155/1999/241046.
Texto completoWood, Anthony C., Yonghong Zhang, Qianxing Mo, Ling Cen, Jacques Fontaine, Sarah E. Hoffe, Jessica Frakes et al. "Evaluation of Tumor DNA Sequencing Results in Patients with Gastric and Gastroesophageal Junction Adenocarcinoma Stratified by TP53 Mutation Status". Oncologist 27, n.º 4 (26 de febrero de 2022): 307–13. http://dx.doi.org/10.1093/oncolo/oyac018.
Texto completoAhn, Jae-Sook, Hyeoung-Joon Kim, Yeo-Kyeoung Kim, Il-Kwon Lee, Nan Young Kim, Mark D. Minden, Chul Won Jung et al. "An Adverse Prognostic Effect of Homozygous TET2 Mutational Status on the Relapse Risk of Acute Myeloid Leukemia Patients of Normal Karyotype". Blood 124, n.º 21 (6 de diciembre de 2014): 1052. http://dx.doi.org/10.1182/blood.v124.21.1052.1052.
Texto completoKang, S., S. S. Seo, H. J. Chang, C. W. Yoo, S. Y. Park y S. M. Dong. "Mutual exclusiveness between PIK3CA and KRAS mutations in endometrial carcinoma". International Journal of Gynecologic Cancer 18, n.º 6 (2008): 1339–43. http://dx.doi.org/10.1111/j.1525-1438.2007.01172.x.
Texto completoFRY, JAMES D. "Rapid mutational declines of viability in Drosophila". Genetical Research 77, n.º 1 (febrero de 2001): 53–60. http://dx.doi.org/10.1017/s0016672300004882.
Texto completoDelaugerre, Constance, Mireille Mouroux, Anne Yvon-Groussin, Anne Simon, Francis Angleraud, Jean-Marie Huraux, Henri Agut, Christine Katlama y Vincent Calvez. "Prevalence and Conditions of Selection of E44D/A and V118I Human Immunodeficiency Virus Type 1 Reverse Transcriptase Mutations in Clinical Practice". Antimicrobial Agents and Chemotherapy 45, n.º 3 (1 de marzo de 2001): 946–48. http://dx.doi.org/10.1128/aac.45.3.946-948.2001.
Texto completoGolding, G. Brian, Patricia J. Gearhart y Barry W. Glickman. "Patterns of Somatic Mutations in Immunoglobulin Variable Genes". Genetics 115, n.º 1 (1 de enero de 1987): 169–76. http://dx.doi.org/10.1093/genetics/115.1.169.
Texto completoDunson, David B. y Kenneth R. Tindall. "Bayesian Analysis of Mutational Spectra". Genetics 156, n.º 3 (1 de noviembre de 2000): 1411–18. http://dx.doi.org/10.1093/genetics/156.3.1411.
Texto completoAstudillo, H., J. Sanchez-Guillen, P. Romero-Garcia, J. Bastarrachea-ortiz, G. Morgan-Villela, J. M. Salazar, V. M. Vazquez-Rivera, H. Ruiz-Calzada y P. Cortes-Esteban. "Polymorphism detection of K-Ras mutations using high-resolution melting analysis in Mexican patients with metastatic colorectal cancer (mCRC)". Journal of Clinical Oncology 27, n.º 15_suppl (20 de mayo de 2009): e15135-e15135. http://dx.doi.org/10.1200/jco.2009.27.15_suppl.e15135.
Texto completoPiombino, Claudia, Angela Toss, Alessandra Bologna, Elisa Gasparini, Vittoria Tarantino, Maria Elisabetta Filieri, Luca Cottafavi et al. "The prognostic role of somatic BRCA mutations in ovarian cancer: Preliminary results from an observational multicenter cohort study." Journal of Clinical Oncology 38, n.º 15_suppl (20 de mayo de 2020): e13674-e13674. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e13674.
Texto completoKuang, Shelley, Sally C. M. Lau, Kieran Sharma, Juehea Lee, Malcolm Isaiah Ryan, Sabine Schmid, Penelope Ann Bradbury et al. "Impact of KRAS mutational variant on response to immunotherapy in metastatic NSCLC." Journal of Clinical Oncology 39, n.º 15_suppl (20 de mayo de 2021): e21127-e21127. http://dx.doi.org/10.1200/jco.2021.39.15_suppl.e21127.
Texto completoBorowczyk, Martyna, Ewelina Szczepanek-Parulska, Szymon Dębicki, Bartłomiej Budny, Małgorzata Janicka-Jedyńska, Lidia Gil, Frederik A. Verburg et al. "High incidence of FLT3 mutations in follicular thyroid cancer: potential therapeutic target in patients with advanced disease stage". Therapeutic Advances in Medical Oncology 12 (enero de 2020): 175883592090753. http://dx.doi.org/10.1177/1758835920907534.
Texto completoMachado, Heather E., Nina Friesgaard Øbro, Emily Mitchell, Megan Davies, Anthony R. Green, Kourosh Saeb-Parsy, Daniel James Hodson, David Kent y Peter J. Campbell. "Life History of Normal Human Lymphocytes Revealed By Somatic Mutations". Blood 134, Supplement_1 (13 de noviembre de 2019): 1045. http://dx.doi.org/10.1182/blood-2019-128188.
Texto completoZeineddine, Fadl, Benjamin Garmezy, Timothy A. Yap y John Paul Y. C. Shen. "PMC: A more precise classifier of POLE mutations to identify candidates for immune therapy." Journal of Clinical Oncology 39, n.º 15_suppl (20 de mayo de 2021): 3548. http://dx.doi.org/10.1200/jco.2021.39.15_suppl.3548.
Texto completoStratton, Michael R. "Abstract PL02-01: The pathogenesis of cancer susceptibility due to inherited DNA repair defects". Cancer Research 82, n.º 12_Supplement (15 de junio de 2022): PL02–01—PL02–01. http://dx.doi.org/10.1158/1538-7445.am2022-pl02-01.
Texto completoJaffar, Nazish, Shahnaz Imdad Kehar, Aliya Zaman, Saadia Akram y Kiran Abbas. "Spectrum of Tp53 gene mutation in basal cell carcinoma and its morphological subtypes in people of color." Professional Medical Journal 26, n.º 10 (10 de octubre de 2019): 1783–88. http://dx.doi.org/10.29309/tpmj/2019.26.10.4141.
Texto completoLee, Ye Ji, Yejin Lee, Youn Jung Kim, Zang Hee Lee y Jung-Wook Kim. "Novel PAX9 Mutations Causing Isolated Oligodontia". Journal of Personalized Medicine 14, n.º 2 (8 de febrero de 2024): 191. http://dx.doi.org/10.3390/jpm14020191.
Texto completoJeffers, Michael, Christian Kappeler, Iris Kuss, Georg Beckmann, Daniel H. Mehnert, Johannes Fredebohm y Michael Teufel. "Broad spectrum of regorafenib activity on mutant KIT and absence of clonal selection in gastrointestinal stromal tumor (GIST): correlative analysis from the GRID trial". Gastric Cancer 25, n.º 3 (20 de enero de 2022): 598–608. http://dx.doi.org/10.1007/s10120-021-01274-6.
Texto completoXu, Hong-Tao, Maureen Oliveira, Peter K. Quashie, Matthew McCallum, Yingshan Han, Yudong Quan, Bluma G. Brenner y Mark A. Wainberg. "Subunit-Selective Mutational Analysis and Tissue Culture Evaluations of the Interactions of the E138K and M184I Mutations in HIV-1 Reverse Transcriptase". Journal of Virology 86, n.º 16 (23 de mayo de 2012): 8422–31. http://dx.doi.org/10.1128/jvi.00271-12.
Texto completoJuriloff, D. M., S. D. Porter y M. J. Harris. "Three spontaneous mutations at the albino locus in SELH/Bc mice". Genome 37, n.º 2 (1 de abril de 1994): 190–97. http://dx.doi.org/10.1139/g94-026.
Texto completoMaldonado, J. Alberto, Chin-Hsien Tai y Christine Alewine. "Genomic characterization of somatic mutations by race and ethnicity in pancreatic cancer defined through AACR project GENIE." Journal of Clinical Oncology 41, n.º 16_suppl (1 de junio de 2023): 4138. http://dx.doi.org/10.1200/jco.2023.41.16_suppl.4138.
Texto completoWiens, G. D., K. A. Heldwein, M. P. Stenzel-Poore y M. B. Rittenberg. "Somatic mutation in VH complementarity-determining region 2 and framework region 2: differential effects on antigen binding and Ig secretion." Journal of Immunology 159, n.º 3 (1 de agosto de 1997): 1293–302. http://dx.doi.org/10.4049/jimmunol.159.3.1293.
Texto completoLin, Selena Y., Ting-Tsung Chang, Jamin D. Steffen, Sitong Chen, Surbhi Jain, Wei Song, Yih-Jyh Lin y Ying-Hsiu Su. "Detection of CTNNB1 Hotspot Mutations in Cell-Free DNA from the Urine of Hepatocellular Carcinoma Patients". Diagnostics 11, n.º 8 (14 de agosto de 2021): 1475. http://dx.doi.org/10.3390/diagnostics11081475.
Texto completoPatterson, Andrew, Abdurrahman Elbasir, Bin Tian y Noam Auslander. "Computational Methods Summarizing Mutational Patterns in Cancer: Promise and Limitations for Clinical Applications". Cancers 15, n.º 7 (24 de marzo de 2023): 1958. http://dx.doi.org/10.3390/cancers15071958.
Texto completoLyons, Daniel y Adam Lauring. "Mutation and Epistasis in Influenza Virus Evolution". Viruses 10, n.º 8 (3 de agosto de 2018): 407. http://dx.doi.org/10.3390/v10080407.
Texto completoHwang, Tae Sook, Wook Youn Kim, Hye Seung Han, So Dug Lim, Wan-Seop Kim, Young Bum Yoo, Kyoung Sik Park, Seo Young Oh, Suk Kyeong Kim y Jung Hyun Yang. "Preoperative RAS Mutational Analysis Is of Great Value in Predicting Follicular Variant of Papillary Thyroid Carcinoma". BioMed Research International 2015 (2015): 1–8. http://dx.doi.org/10.1155/2015/697068.
Texto completoThomas, Renjan, Gautam Balaram, Hrishi Varayathu, Suhas N. Ghorpade, Prarthana V. Kowsik, Baby Dharman, Beulah Elsa Thomas et al. "Molecular epidemiology and clinical characteristics of epidermal growth factor receptor mutations in NSCLC: A single-center experience from India". Journal of Cancer Research and Therapeutics 19, n.º 5 (2023): 1398–406. http://dx.doi.org/10.4103/jcrt.jcrt_1986_21.
Texto completoIto-Harashima, Sayoko, Phillip E. Hartzog, Himanshu Sinha y John H. McCusker. "The tRNA-Tyr Gene Family ofSaccharomyces cerevisiae: Agents of Phenotypic Variation and Position Effects on Mutation Frequency". Genetics 161, n.º 4 (1 de agosto de 2002): 1395–410. http://dx.doi.org/10.1093/genetics/161.4.1395.
Texto completoKeightley, Peter D. y Ohmi Ohnishi. "EMS-Induced Polygenic Mutation Rates for Nine Quantitative Characters in Drosophila melanogaster". Genetics 148, n.º 2 (1 de febrero de 1998): 753–66. http://dx.doi.org/10.1093/genetics/148.2.753.
Texto completoAlohali, Sama, Alexandra E. Payne, Marc Pusztaszeri, Mohannad Rajab, Véronique-Isabelle Forest, Michael P. Hier, Michael Tamilia y Richard J. Payne. "Effect of Having Concurrent Mutations on the Degree of Aggressiveness in Patients with Thyroid Cancer Positive for TERT Promoter Mutations". Cancers 15, n.º 2 (8 de enero de 2023): 413. http://dx.doi.org/10.3390/cancers15020413.
Texto completoLi, Hongxia, Qianqian Duan y Yuan Tan. "Somatic and germline mutation profiles of Chinese young colorectal cancer patients." Journal of Clinical Oncology 39, n.º 15_suppl (20 de mayo de 2021): e15522-e15522. http://dx.doi.org/10.1200/jco.2021.39.15_suppl.e15522.
Texto completoHa, Jung Sook, Jae Hee Lee, Sung Gyun Park, Nam Hee Ryoo, Dong Suk Jeon, Jae Ryong Kim, Young Rok Do et al. "Correlations Between TET2 Mutation and Clinicohematologic Parameters in Myeloproliferative Neoplasms". Blood 120, n.º 21 (16 de noviembre de 2012): 1455. http://dx.doi.org/10.1182/blood.v120.21.1455.1455.
Texto completoMüller, Martin C., Jorge Cortes, Dong-Wook Kim, Brian J. Druker, Philipp Erben, Ricardo Pasquini, Timothy P. Hughes, Yousif Matloub, Lynn Ploughman y Andreas Hochhaus. "Dasatinib Efficacy in Patients with Chronic Myeloid Leukemia in Chronic Phase (CML-CP) and Pre-Existing BCR-ABL Mutations". Blood 112, n.º 11 (16 de noviembre de 2008): 449. http://dx.doi.org/10.1182/blood.v112.11.449.449.
Texto completoHughes, Timothy, Giuseppe Saglio, Giovanni Martinelli, Dong-Wook Kim, S. Soverini, Martin Mueller, A. Haque et al. "Responses and Disease Progression in CML-CP Patients Treated with Nilotinib after Imatinib Failure Appear To Be Affected by the BCR-ABL Mutation Status and Types." Blood 110, n.º 11 (16 de noviembre de 2007): 320. http://dx.doi.org/10.1182/blood.v110.11.320.320.
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