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196321por González-Moles, Miguel Ángel, Moya-González, Eloísa, García-Ferrera, Alberto, Nieto-Casado, Paola, Ramos-García, Pablo“…On the other hand, TERT gene mutations obtained constantly nonsignificant null effect sizes for all outcomes investigated, evidencing no prognostic or clinicopathological value. …”
Publicado 2022
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196322por Shahapur, Praveen R, Shahapur, Roopa, Kandi, Venkataramana, Suvvari, Tarun Kumar, Vadakedath, Sabitha“…The virus is undergoing mutations and is evolving into variants that are responsible for wave after wave. …”
Publicado 2022
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196323“…CONCLUSIONS AND RELEVANCE: The findings of this study suggest that SARS-CoV-2 has evolved and mutated continuously throughout the COVID-19 pandemic, producing variants with different enhanced transmission and virulence. …”
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196324por Iqbal, Naveed, Rafiq, Muhammad, Masooma, Tareen, Sanaullah, Ahmad, Maqsood, Nawaz, Faheem, Khan, Sumair, Riaz, Rida, Yang, Ting, Fatima, Ambrin, Jamal, Muhsin, Mansoor, Shahid, Liu, Xin, Ahmed, Nazeer“…Recent studies showed that various environmental selection pressures challenge the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infectivity and, in response, the virus engenders new mutations, leading to the emergence of more virulent strains of WHO concern. …”
Publicado 2022
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196325por Laukka, Jeremy J, Kain, Kevin M, Rathnam, Anirudha S, Sohi, Jasloveleen, Khatib, Dalal, Kamholz, John, Stanley, Jeffrey A“…Pelizaeus–Merzbacher disease is an X-linked recessive leucodystrophy of the central nervous system caused by mutations affecting the major myelin protein, proteolipid protein 1. …”
Publicado 2022
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196326por Prabhakar, Apurva T., James, Claire D., Das, Dipon, Fontan, Christian T., Otoa, Raymonde, Wang, Xu, Bristol, Molly L., Morgan, Iain M.“…Here, we demonstrate that in U2OS cells expressing wild-type E2 and a non-TopBP1-binding mutant (S23A, serine 23 mutated to alanine), interaction with TopBP1 is essential for E2 recruitment of plasmids to mitotic chromatin. …”
Publicado 2022
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196327por Camidge, D. Ross, Morgensztern, Daniel, Heist, Rebecca S., Barve, Minal, Vokes, Everett, Goldman, Jonathan W., Hong, David S., Bauer, Todd M., Strickler, John H., Angevin, Eric, Motwani, Monica, Parikh, Apurvasena, Sun, Zhaowen, Bach, Bruce Allen, Wu, Jun, Komarnitsky, Philip B., Kelly, Karen“…The dose-expansion phase enrolled patients with NSCLC and c-Met H-score ≥150 (c-Met+) or MET amplification/exon 14 skipping mutations. Safety, pharmacokinetics, and efficacy were assessed. …”
Publicado 2021
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196328por Milinski, Manfred“…Synthesized peptides supplemented to a male’s signal affect choice in the predicted way, however, not when anchors are mutated. Also, the human brain detects smelled synthesized self-peptides as such. …”
Publicado 2022
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196329por Shirasaki, Takayoshi, Feng, Hui, Duyvesteyn, Helen M. E., Fusco, William G., McKnight, Kevin L., Xie, Ling, Boyce, Mark, Kumar, Sathish, Barouch-Bentov, Rina, González-López, Olga, McNamara, Ryan, Wang, Li, Hertel-Wulff, Adriana, Chen, Xian, Einav, Shirit, Duncan, Joseph A., Kapustina, Maryna, Fry, Elizabeth E., Stuart, David I., Lemon, Stanley M.“…Fusing pX to a self-assembling engineered protein nanocage (EPN-pX) resulted in its ESCRT-dependent release in extracellular vesicles. Mutational analysis identified a 24 amino acid peptide sequence located within the center of pX that was both necessary and sufficient for nanocage release. …”
Publicado 2022
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196330por Li, Jie, Zhang, Liuyang, Xu, Qing, Zhang, Wenting, Li, Zhihua, Chen, Lei, Dong, Xiuzhu“…Further, as a proof of concept, precise mutagenesis at the nucleotide level allowed the engineering of both transcriptional and translational activities. Mutations were introduced into an archaeal promoter BRE (transcription factor B [TFB] recognition element), a terminator U-tract region, and a gene coding region. …”
Publicado 2022
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196331por Li, Xinhui, Zhang, Jisheng, Yang, Chengru, Li, Jie, Wang, Jianmin, Huang, Wan, Zeng, Lingyi, Liang, Xushan, Long, Wenzhang, Zhang, Xiaoli“…Four reduced-susceptibility strains evolved resistance under selective pressure of CAZ/AVI with the bla(KPC-2) expression level increased, and two of these strains had mutations in the Ω-loop. The study found a strain of CRKP55 with changes in the resistance phenotype during conjugation, evolving from reduced sensitivity to high-level resistance to CAZ/AVI. …”
Publicado 2022
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196332por Navarro-Lleó, Noemi, Santiso-Bellón, Cristina, Vila-Vicent, Susana, Carmona-Vicente, Noelia, Gozalbo-Rovira, Roberto, Cárcamo-Calvo, Roberto, Rodríguez-Díaz, Jesús, Buesa, Javier“…Noroviruses show wide genetic variability due to a high rate of mutations but also due to genomic recombinations, as we demonstrate in this study. …”
Publicado 2022
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196333“…Loss-of-function (LOF) mutated allele was included in 56.9% of CYP2C19 genotypes, and their corresponding phenotypes were intermediate metabolizers (46.2%) and poor metabolizers (10.7%). (2) The incidence of CR in this study population was 31.4%. …”
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196334por Qian, Xiaoyu, Guo, Xiaodan, Li, Ting, Hu, Wei, Zhang, Lin, Wu, Caisheng, Ye, Feng“…Background: Epidermal growth factor receptor (EGFR) mutations are common in patients with non-small-cell lung cancer (NSCLC), particularly in Asian populations. …”
Publicado 2022
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196335“…Protonation and deprotonation of the conserved carboxyl group on each c-subunit is facilitated by separate groups of subunit-a residues, which were determined to have different pKa’s. Mutations of any of any residue from either group changed both pKa values, which changed the occurrence of the 11° rotation proportionately. …”
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196336por Zhang, Ting, Zhu, Shasha, Miao, Haixia, Yang, Jianbin, Shi, Yezhen, Yue, Yuwei, Zhang, Yu, Yang, Rulai, Wu, Benqing, Huang, Xinwen“…All abnormal characteristic metabolic indicators in the “Newborn-screen Group” came back to normal levels at earlier ages than the “Clinical diagnosed Group.” c.852_855del (41.2%), IVS16ins3kb (17.6%), c.615 + 5G>A (9.6%), 1638_1660dup (4.4%), and c.1177 + 1G>A (3.7%) accounted for 76.5% of all the mutated SLC25A13 alleles in our population. Conclusion: Argininosuccinate synthesis, gluconeogenesis, ketogenesis, fatty acid oxidation, liver function, and cholestasis were more severely affected in the “Clinical diagnosed Group.” …”
Publicado 2022
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196337por Keulers, Tom G., Koch, Alexander, van Gisbergen, Marike W., Barbeau, Lydie M.O., Zonneveld, Marijke I., de Jong, Monique C., Savelkouls, Kim G.M., Wanders, Roel G., Bussink, Johan, Melotte, Veerle, Rouschop, Kasper M.A.“…Paradoxically, in several cancer types, mutations or loss of essential autophagy genes have been reported that are associated with earlier onset of tumor growth. …”
Publicado 2021
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196338por Verduri, Alessia, Short, Roxanna, Carter, Ben, Braude, Philip, Vilches-Moraga, Arturo, Quinn, Terence J, Collins, Jemima, Lumsden, Jane, McCarthy, Kathryn, Evans, Louis, Myint, Phyo K, Hewitt, Jonathan“…BACKGROUND: Effective shielding measures and virus mutations have progressively modified the disease between the waves, likewise healthcare systems have adapted to the outbreak. …”
Publicado 2022
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196339por Lassche, Gerben, van Helvert, Sjoerd, Eijkelenboom, Astrid, Tjan, Martijn J. H., Jansen, Erik A. M., van Cleef, Patricia H. J., Verhaegh, Gerald W., Kamping, Eveline J., Grünberg, Katrien, van Engen-van Grunsven, Adriana C. H., Ligtenberg, Marjolijn J. L., van Herpen, Carla M. L.“…This research aimed to identify these actionable aberrations by combining NGS-based analysis of RNA (gene fusions) and DNA (single and multiple nucleotide variants, copy number variants, microsatellite instability and tumor mutational burden) in a large cohort of SGC patients. …”
Publicado 2022
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196340por Cruz-Nova, Pedro, Ocampo-García, Blanca, Carrión-Estrada, Dayan Andrea, Briseño-Diaz, Paola, Ferro-Flores, Guillermina, Jiménez-Mancilla, Nallely, Correa-Basurto, José, Bello, Martiniano, Vega-Loyo, Libia, Thompson-Bonilla, María del Rocío, Hernández-Rivas, Rosaura, Vargas, Miguel“…In 40–50% of colorectal cancer (CRC) cases, K-Ras gene mutations occur, which induce the expression of the K-Ras4B oncogenic isoform. …”
Publicado 2022
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