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1081por Liu, Chuan, Jin, Yuzhi, Zhang, Hangyu, Yan, Junrong, Guo, Yixuan, Bao, Xuanwen, Zhao, Peng“…BACKGROUND: KMT2D mutation (KMT2D(MT)) was found to play an important role in cancer immunity and response to immune checkpoint inhibitors (ICIs). …”
Publicado 2023
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1082por Han, Jialong, Wang, Ya, Zhong, Lili, Zhou, Huijie, Yu, Min, Li, Yanying, Lu, You, Wang, Yan, Zhu, Jiang“…This case report demonstrates a rare mutation pattern in a male patient with a pathologic diagnosis of non-small cell lung cancer (NSCLC) harboring an EGFR exon 19 deletion (19Del) mutation, who then acquired an EGFR-T790M mutation after developing resistance to the first generation EGFR-TKI (gefitinib). …”
Publicado 2018
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1083“…In this work we determine the transformations of these single-centered indices under mutations. Moreover, we generalize these mutations to quivers whose nodes carry single-centered indices different from unity. …”
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1084“…The discussion is based on a number of new methods, in particular multiple scale analysis, nonlinear Markov processes and their entrance laws, atomic measure-valued evolutions and new forms of duality (for state-dependent mutation and multitype selection) which are used to prove ergodic theorems in this context and are applicable for many other questions and renormalization analysis for a variety of phenomena (stasis, punctuated equilibrium, failure of naive branching approximations, biodiversity) which occur due to the combination of rare mutation, mutation, resampling, migration and selection and make it necessary to mathematically bridge the gap (in the limit) between time and space scales.…”
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1085por Temaj, Gazmend, Telkoparan-Akillilar, Pelin, Nuhii, Nexhibe, Chichiarelli, Silvia, Saha, Sarmistha, Saso, Luciano“…Approximately 11% of genetic human diseases are caused by nonsense mutations that introduce a premature termination codon (PTC) into the coding sequence. …”
Publicado 2023
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1086“…Somatic mutations of calreticulin (CRT), an endoplasmic reticulum (ER)‐localized lectin chaperone, are driver mutations in approximately 25% of ET and 35% of MF patients. …”
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1087por Cote-L’Heureux, Auden, Maithania, Yogesh NK, Franco, Melissa, Khrapko, Konstantin“…A large-scale study of mutations in mitochondrial DNA has revealed a subset that do not accumulate with age.…”
Publicado 2023
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1088“…For prioritization of noncoding mutations in imbalanced datasets, the ReMM score performed much better than other variation scores. …”
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1089por Hong, Junshik“…Increasing knowledge of the molecular features of myeloproliferative neoplasms (MPNs) is being combined with existing prognostic models based on clinical, laboratory, and cytogenetic information. Mutation-enhanced international prognostic systems (MIPSS) for polycythemia vera (PV) and essential thrombocythemia (ET) have improved prognostic assessments. …”
Publicado 2023
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1090“…SIMPLE SUMMARY: More than a third of all colorectal cancers have a KRAS mutation. The complex biology of these cancers has challenged the development of direct targeting inhibitors. …”
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1091por Besselink, Nicolle, Keijer, Janneke, Vermeulen, Carlo, Boymans, Sander, de Ridder, Jeroen, van Hoeck, Arne, Cuppen, Edwin, Kuijk, Ewart“…However, there was no increase in mutational burden, enrichment for certain mutational signatures or accumulation of structural variation to the genome. …”
Publicado 2023
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1092por Tlais, Dana, Barros Guinle, Maria Isabel, Wheeler, Joshua Riley, Prolo, Laura M, Vogel, Hannes, Partap, SoniaEnlace del recurso
Publicado 2023
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1093“…PM(2.5) increases EGFR pre-mutated alveolar type II cell progenitor function and tumorigenic activity through interstitial macrophage-secreted IL-1β, providing potential prevention approaches to inhibit cancer initiation.…”
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1094por Saldivar-Espinoza, Bryan, Garcia-Segura, Pol, Novau-Ferré, Nil, Macip, Guillem, Martínez, Ruben, Puigbò, Pere, Cereto-Massagué, Adrià, Pujadas, Gerard, Garcia-Vallve, Santiago“…Mutation research is crucial for detecting and treating SARS-CoV-2 and developing vaccines. …”
Publicado 2023
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1096“…Epidermal growth factor receptor (EGFR) mutations are important events in carcinogenesis. The present study summarized the common germline mutations of EGFR, including T790M, V843I, R776H and P848L, and provided detailed information regarding each mutation site and potential treatment strategies. …”
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1098por Sood, Mansi, Sridhar, Anirudh, Eletreby, Rashad, Wu, Chai Wah, Levin, Simon A., Yağan, Osman, Poor, H. Vincent“…Most epidemiological models do not consider the role of mutations and heterogeneity in the type of contact events. …”
Publicado 2023
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1099“…This approach formalizes our proposal that most mutations have a lower mutation rate than the average mutation rate measured experimentally. …”
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1100“…Somatic mutations have important biological ramifications while exerting substantial rate, type, and genomic location heterogeneity. …”
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