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195821por Qiu, Xusheng, Meng, Chunchun, Zhan, Yuan, Yu, Shengqing, Li, Shichao, Ren, Tingting, Yuan, Weifeng, Xu, Shuqin, Sun, Yingjie, Tan, Lei, Song, Cuiping, Liao, Ying, Ding, Zhuang, Liu, Xiufan, Ding, Chan“…The R value was calculated based on cross hemagglutination inhibition and cross virus neutralization results, and confirmed antigenic difference of the PPMV-1 strains isolated in 2013 from the LaSota vaccine strain. Several mutations were identified in the surface glycoproteins F and HN, which probably gave rise to those antigenic differences. …”
Publicado 2017
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195822por Forero, Andrea, Rivero, Olga, Wäldchen, Sina, Ku, Hsing-Ping, Kiser, Dominik P., Gärtner, Yvonne, Pennington, Laura S., Waider, Jonas, Gaspar, Patricia, Jansch, Charline, Edenhofer, Frank, Resink, Thérèse J., Blum, Robert, Sauer, Markus, Lesch, Klaus-Peter“…The consequence of CDH13 loss-of-function mutations on brain 5-HT system development was explored in a mouse model of Cdh13 deficiency. …”
Publicado 2017
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195823por Audoux, Jérôme, Salson, Mikaël, Grosset, Christophe F., Beaumeunier, Sacha, Holder, Jean-Marc, Commes, Thérèse, Philippe, Nicolas“…SimCT generates simulated datasets that get as close as possible to specific real biological conditions accompanied by the list of genomic incidents and mutations that have been inserted. BenchCT then compares the output of any bioinformatics pipeline that has been run against a SimCT dataset with the simulated genomic and transcriptional variations it contains to give an accurate performance evaluation in addressing specific biological question. …”
Publicado 2017
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195824por Vashee, Sanjay, Stockwell, Timothy B., Alperovich, Nina, Denisova, Evgeniya A., Gibson, Daniel G., Cady, Kyle C., Miller, Kristofer, Kannan, Krishna, Malouli, Daniel, Crawford, Lindsey B., Voorhies, Alexander A., Bruening, Eric, Caposio, Patrizia, Früh, Klaus“…However, this process is inefficient, results in adaptive mutations, and involves deletion of viral genes to avoid oversized genomes when inserting the BAC cassette. …”
Publicado 2017
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195825“…CONCLUSIONS: The CEG repertoires of related pathogens diverged dramatically in short evolutionary times because of rapid turnover and of positive selection fixing non-synonymous mutations. While signatures of positive selection on effector sequences are the expected outcome of the evolutionary “arms race” between pathogen and plant immune system, it is more difficult to infer the mechanisms and evolutionary forces that maintained an extreme turnover rate in CEG families of B. graminis for several millions of years. …”
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195826por Jamal, Rahima, Lapointe, Réjean, Cocolakis, Eftihia, Thébault, Paméla, Kazemi, Shirin, Friedmann, Jennifer E., Dionne, Jeanne, Cailhier, Jean-François, Bélanger, Karl, Ayoub, Jean-Pierre, Le, Huy, Lambert, Caroline, El-Hajjar, Jida, van Kempen, Léon C., Spatz, Alan, Miller, Wilson H.“…Response to treatment was positively correlated with a higher tumor CD3(+) infiltrate (immune score) at baseline. NRAS and BRAF mutations were less frequent in patients who experienced clinical benefit. …”
Publicado 2017
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195827por Ouattara, Abdoul Karim, Yameogo, Pouiré, Traore, Lassina, Diarra, Birama, Assih, Maléki, Compaore, Tegwindé Rébéca, Obiri-yeboah, Dorcas, Soubeiga, Serge Théophile, Djigma, Florencia Wendkuuni, Simpore, Jacques“…METHODS: A systematic review was carried out to analyze available published data on the prevalence, phenotypes and mutations responsible for G-6-PD deficiency in Burkina Faso. …”
Publicado 2017
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195828por Wang, Liming, Gu, Haiyong, Long, Tao, Pan, Huiwen, Lv, Lu, Shi, Yijun, Zhu, Jingfeng, Sun, Yangyong, Tang, Weifeng, Ding, Guowen, Chen, Suocheng, Fan, Yu, Ding, Hao, Qian, Cheng, Wang, Qun, Yao, Jun, Tan, Lijie, Yin, Jun“…However, larger studies among different ethnic populations and further experiments using genetically mutated cells or animals are warranted to verify our conclusion.…”
Publicado 2017
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195829por Luo, Guo, Lin, Ling, Jacob, Louis, Bonvalet, Mélodie, Ambati, Aditya, Plazzi, Giuseppe, Pizza, Fabio, Leib, Ryan, Adams, Christopher M., Partinen, Markku, Mignot, Emmanuel Jean-Marie“…Anti-HCRTR2 autoantibodies were detected using three strategies: (1) Human embryonic kidney (HEK) 293T cells with transient expression of HCRTR2 were stained with human sera and then analyzed by flow cytometer; (2) In vitro translation of [(35)S]-radiolabelled HCRTR2 was incubated with human sera and immune complexes of autoantibody and [(35)S]-radiolabelled HCRTR2 were quantified using a radioligand-binding assay; (3) Optical density (OD) at 450 nm (OD450) of human serum immunoglobulin G (IgG) binding to HCRTR2 stably expressed in Chinese hamster ovary (CHO)-K1 cell line was measured using an in-cell enzyme-linked immunosorbent assay (ELISA). RESULTS: NP 116M mutations were predominantly present in all batches of Pandemrix(®), Arepanrix(®) and Focetria(®). …”
Publicado 2017
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195830por Yan, Zhipeng, Tong, Xiang, Ma, Yao, Liu, Sitong, Yang, Lingjing, Yang, Xin, Yang, Xue, Bai, Min, Fan, Hong“…The ataxia telangiectasia mutated (ATM) gene plays an important role in the DNA DSB repair pathway. …”
Publicado 2017
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195831por Marks, Lianna J., Oberg, Jennifer A., Pendrick, Danielle, Sireci, Anthony N., Glasser, Chana, Coval, Carrie, Zylber, Rebecca J., Chung, Wendy K., Pang, Jiuhong, Turk, Andrew T., Hsiao, Susan J., Mansukhani, Mahesh M., Glade Bender, Julia L., Kung, Andrew L., Sulis, Maria Luisa“…CONCLUSION: Incorporating whole exome and transcriptome profiling of tumor and normal tissue into clinical practice is feasible, and the value that comprehensive testing provides extends beyond the ability to target-specific mutations.…”
Publicado 2017
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195832por Ji, Xiaoqian, Chen, Siyu, Guo, Yanwu, Li, Wende, Qi, Xiaolong, Yang, Han, Xiao, Sa, Fang, Guang, Hu, Jinfang, Wen, Chuangyu, Liu, Huanliang, Han, Zhen, Deng, Guangxu, Yang, Qingbin, Yang, Xiangling, Xu, Yuting, Peng, Zhihong, Li, Fengping, Cai, Nvlue, Li, Guoxin, Huang, Ren“…BACKGROUND: Patient-derived xenografts (PDX) have a biologically stable in tumor architecture, drug responsiveness, mutational status and global gene-expression patterns. …”
Publicado 2017
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195833por Choudhary, Preeti, Kumar, Shailesh, Bachhawat, Anand Kumar, Pandit, Shashi Bhushan“…Hence, such predictions can assist experimentalist to prioritize residues for mutational studies in their efforts to characterize catalytic residues. …”
Publicado 2017
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195834“…Conversely, deleterious point mutations of this gene do not show any clinical phenotypes. …”
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195835por Jun, Se-Ran, Wassenaar, Trudy M., Wanchai, Visanu, Patumcharoenpol, Preecha, Nookaew, Intawat, Ussery, David W.“…A number of these positively selected mutations resulted in an increased potential to be phosphorylated in the Brazilian lineage compared to the African linage, which may have increased their potential to interfere with neural fetal development. …”
Publicado 2017
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195836por Böttcher, René, Kweldam, Charlotte F., Livingstone, Julie, Lalonde, Emilie, Yamaguchi, Takafumi N., Huang, Vincent, Yousif, Fouad, Fraser, Michael, Bristow, Robert G., van der Kwast, Theodorus, Boutros, Paul C., Jenster, Guido, van Leenders, Geert J. L. H.“…Several of the affected genes were known to be associated with aggressive prostate cancer such as loss of PTEN, CDH1, BCAR1 and gain of MYC. Point mutations in TP53, SPOP and FOXA1were also associated with CR/IDC, but occurred less frequently than CNAs. …”
Publicado 2018
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195837por Hölscher, Alexander S., Schulz, Wolfgang A., Pinkerneil, Maria, Niegisch, Günter, Hoffmann, Michèle J.“…Small-molecule drugs targeting chromatin regulators are reasonable candidates because these regulators are frequently mutated or deregulated in UC. Indeed, in previous work, Romidepsin, which targets class I histone deacetylases (HDAC), efficiently killed UC cells, but did not elicit canonical apoptosis and affected benign urothelial cells indiscriminately. …”
Publicado 2018
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195838por Srisutham, Suttipat, Saralamba, Naowarat, Sriprawat, Kanlaya, Mayxay, Mayfong, Smithuis, Frank, Nosten, Francois, Pukrittayakamee, Sasithon, Day, Nicholas P. J., Dondorp, Arjen M., Imwong, Mallika“…For further vaccine development, carboxyl terminal of P48/45 would be a good candidate according to conserved amino acid at low genetic diversity (π = 0.2–0.3). CONCLUSIONS: High mutational diversity was observed in P. malariae trap and ama1 as compared to p48/45 in P. malariae samples isolated from Thailand, Myanmar, and Lao PDR. …”
Publicado 2018
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195839por Kim, Dong Kyu, Park, Joonho, Han, Dohyun, Yang, Jinhee, Kim, Ahbin, Woo, Jongmin, Kim, Youngsoo, Mook-Jung, Inhee“…The ADLP(APT) mice carry three human transgenes, including amyloid precursor protein, presenilin-1, and tau, with six mutations. To characterize the molecular and functional signatures of AD in ADLP(APT) mice, we analyzed the hippocampal proteome and performed comparisons with individual-pathology transgenic mice (i.e., amyloid or neurofibrillary tangles) and wild-type mice using quantitative proteomics with 10-plex tandem mass tag. …”
Publicado 2018
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195840por Chen, Yiran, Xie, Xiaoling, Wu, Anqin, Wang, Lei, Hu, Yuxing, Zhang, Honghao, Li, Yuhua“…A specific peptide (CP-EPS8-NLS) derived from the NLS of EPS8 (amino acids 298–310) was synthesized, and the anti-AML effects of CP-EPS8-NLS were analyzed in cancer cells and in xenograft models. Mutated CP-EPS8-NLS and penetratin served as controls. …”
Publicado 2018
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