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194141por Pech-May, Angélica, Ramsey, Janine M., González Ittig, Raúl E., Giuliani, Magali, Berrozpe, Pablo, Quintana, María G., Salomón, Oscar D.“…At least eight haplogroups (three of these identified in Argentina), each separated by multiple mutational steps using the ND4, are differentiated across the Neotropical realm. …”
Publicado 2018
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194142por Shen, Jia, Zhang, Tao, Cheng, Zheng, Zhu, Ni, Wang, Hua, Lin, Li, Wang, Zexia, Yi, Haotian, Hu, Meichun“…Epidermal Growth Factor Receptor (EGFR) gene amplification and mutations are the most common oncogenic events in GBM. …”
Publicado 2018
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194143por Sun, Jiaoli, Li, Ningbo, Duan, Guangyou, Liu, Yi, Guo, Shanna, Wang, Cong, Zhu, Changmao, Zhang, Xianwei“…Na(v)1.7, in particular, of which mutations in the encoding gene (SCN9A) can determine whether pain occurs, has aroused most attention. …”
Publicado 2018
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194144“…The vaccine encodes a fusion protein composed of a truncated HBV core protein, mutated polymerase protein, and two envelope domains. …”
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194145por Yan, S. Betty, Um, Suzane L., Peek, Victoria L., Stephens, Jennifer R., Zeng, Wei, Konicek, Bruce W., Liu, Ling, Manro, Jason R., Wacheck, Volker, Walgren, Richard A.“…Purpose Approximately 3% of lung cancer bears mutations leading to MET exon 14 skipping, an oncogenic driver which is further evidenced by case reports of patient response to MET kinase inhibitor treatment. …”
Publicado 2017
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194146por Yoshida, Go J.“…That is why the loss-of-functional mutations of FBW7 gene are expected to trigger “awakening” of dormant CSCs in the niche with c-Myc up-regulation. …”
Publicado 2018
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194147por Robbins, Jacqueline P., Perfect, Leo, Ribe, Elena M., Maresca, Marcello, Dangla-Valls, Adrià, Foster, Evangeline M., Killick, Richard, Nowosiad, Paulina, Reid, Matthew J., Polit, Lucia Dutan, Nevado, Alejo J., Ebner, Daniel, Bohlooly-Y, Mohammad, Buckley, Noel, Pangalos, Menelas N., Price, Jack, Lovestone, Simon“…Advances in identifying components of the amyloid cascade are progressing, including the role of the protein clusterin in mediating β-amyloid (Aβ) toxicity. Mutations in the clusterin gene (CLU), a major genetic AD risk factor, are known to have important roles in Aβ processing. …”
Publicado 2018
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194148“…The 5‐year OS for drug‐resistant recurrent ovarian cancer patients (44 ± 11.07 months, 95% CI: 231.24–53.66 months) was significantly lower than that of drug‐sensitive recurrent ovarian cancer patients (58 ± 3.97 months; 95% CI: 50.05–65.59 months; p = 0.024) TP53 was the most frequently mutated gene in both drug‐resistant (9/10, 90%) and drug‐sensitive recurrent ovarian cancers (10/11, 91%). …”
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194149por Tian, Jun, Vemula, Satya R., Xiao, Jianfeng, Valente, Enza Maria, Defazio, Giovanni, Petrucci, Simona, Gigante, Angelo Fabio, Rudzińska‐Bar, Monika, Wszolek, Zbigniew K., Kennelly, Kathleen D., Uitti, Ryan J., van Gerpen, Jay A., Hedera, Peter, Trimble, Elizabeth J., LeDoux, Mark S.“…To our knowledge, none of these genes have previously been associated with isolated BSP, although other CACNA1A mutations have been associated with both positive and negative motor disorders including ataxia, episodic ataxia, hemiplegic migraine, and dystonia. …”
Publicado 2018
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194150“…Antiretroviral resistance mutations were defined using the 2017 International AIDS Society-USA HIV drug resistance algorithm, and drug resistance was compared using the HIVdb program of the Stanford University HIV Drug Resistance Database. …”
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194151por Chen, Xu, Wu, Lei, Li, Dezhi, Xu, Yanmei, Zhang, Luping, Niu, Kai, Kong, Rui, Gu, Jiaoyang, Xu, Zihan, Chen, Zhengtang, Sun, Jianguo“…Dual luciferase report system and miR‐18a‐5p overexpression identified ataxia telangiectasia mutated (ATM) and hypoxia inducible factor 1 alpha (HIF‐1α) as the targets of miR‐18a‐5p. …”
Publicado 2018
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194152“…In neurons, FMRP acts as a translational repressor under activity-dependent control and is mutated in Fragile X Syndrome (FXS). Knock-down of endogenous NG2 in primary OPC reduced translation and mTOR/p70S6K1 phosphorylation in Oli-neu. …”
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194153por Oh, Stephanie E., Park, Hye-Jin, He, Liqiang, Skibiel, Catherine, Junn, Eunsung, Mouradian, M. Maral“…DJ-1 is a highly conserved protein that protects neurons against oxidative stress and whose loss of function mutations are linked to recessively inherited Parkinson's disease (PD). …”
Publicado 2018
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194154por Rooney, John, Oshida, Keiyu, Vasani, Naresh, Vallanat, Beena, Ryan, Natalia, Chorley, Brian N., Wang, Xuting, Bell, Douglas A., Wu, Kai C., Aleksunes, Lauren M., Klaassen, Curtis D., Kensler, Thomas W., Corton, J. Christopher“…Nrf2 was activated in 5 models of disrupted GH signaling containing mutations in Pit1, Prop1, Ghrh, Ghrhr, and Ghr. Out of 59 chemical treatments that activated Nrf2, 36 exhibited STAT5b suppression in the male liver. …”
Publicado 2018
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194155por Bui, Huyen, Greenhalgh, Robert, Ruckert, Alice, Gill, Gunbharpur S., Lee, Sarah, Ramirez, Ricardo A., Clark, Richard M.“…On maize plants harboring mutations in several benzoxazinoid biosynthesis genes, T. urticae performance dramatically increased compared to wild-type plants. …”
Publicado 2018
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194156por Chandy, Mark, Ishida, Masayoshi, Shikatani, Eric A., El-Mounayri, Omar, Park, Lawrence Changsu, Afroze, Talat, Wang, Tao, Marsden, Philip A., Husain, Mansoor“…PP-reporter constructs revealed that point mutations in MBS1 and MBS4 abrogated c-Myb-dependent transcription from the miR-143/145 PP (P<0.01). …”
Publicado 2018
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194157“…RESULTS: 2-hydroxyglutarate, an oncometabolite associated with gliomas with IDH mutations, was successfully detected and assigned by both (1)H-(13)C HSQC and (1)H-(1)H COSY experiments as well as (1)H 1D experiments in two of the tissue samples. …”
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194158por Wang, Tianying, Sinha, Adya Saran, Akita, Tenpei, Yanagawa, Yuchio, Fukuda, Atsuo“…Exposure to prenatal stress (PS) and mutations in Gad1, which encodes GABA synthesizing enzyme glutamate decarboxylase (GAD) 67, are the primary risk factors for psychiatric disorders associated with abnormalities in parvalbumin (PV)-positive GABAergic interneurons in the medial prefrontal cortex (mPFC). …”
Publicado 2018
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194159por Radford, Devon, Strange, Philip, Lepp, Dion, Hernandez, Marta, Rehman, Muhammad Attiq, Diarra, Moussa Sory, Balamurugan, S.“…Genetic and abundance changes to specific carbon and nitrogen metabolism enzymes, not traditionally associated with beta-lactam metabolism, establish an enzymatic framework with the potential to detoxify/degrade ceftiofur, while mutations and changes in subcellular localization in specific cell surface factors enhance the stability of the Gram-negative cell envelop despite the compromising effect of ceftiofur. …”
Publicado 2018
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194160por Simonsen, Anita T., Hansen, Marcus C., Kjeldsen, Eigil, Møller, Peter L., Hindkjær, Johnny J., Hokland, Peter, Aggerholm, Anni“…In this setting, known OCI-AML3 mutations as well as large copy number alterations could be identified, adding to the current knowledge of cytogenetic status. …”
Publicado 2018
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