Materias dentro de su búsqueda.
Materias dentro de su búsqueda.
Historia
6
Genética
4
Condiciones económicas
3
Biología molecular
2
Campesinos
2
Condiciones sociales
2
Evolución (Biología)
2
Francia
2
Genética humana
2
ADN
1
Adaptación (Biología)
1
Administración
1
Agentes antineoplásicos
1
Agricultura
1
Agricultura y Estado
1
Algoritmos en informática
1
Algoritmos genéticos
1
América Latina
1
Aprendizaje colaborativo
1
Asociaciones
1
Aspectos económicos
1
Aspectos moleculares
1
Aspectos sociales
1
Aspectos sociológicos
1
Banano
1
Cambio social
1
Capitalismo
1
Civilización
1
Clubes
1
Condiciones rurales
1
-
196261“…The m(6)A scores calculated based on co-DEGs in these modification patterns were significantly positively correlated with immune infiltration and significantly negatively correlated with tumour mutational burden (TMB). Survival was significantly better in the high-m(6)A-score group than in the low-m(6)A-score group, and the m(6)A score could be used as an independent favourable prognostic factor. …”
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196262por Garziano, Micaela, Utyro, Olga, Poliseno, Mariacristina, Santantonio, Teresa Antonia, Saulle, Irma, Strizzi, Sergio, Lo Caputo, Sergio, Clerici, Mario, Introini, Andrea, Biasin, Mara“…Nevertheless, the presence of immune escape mutations as possibly represented by the SARS-CoV-2 Delta variant negatively affects both local and systemic efficacy of NA associated with vaccination.…”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196263por Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Glessner, Joseph, Sleiman, Patrick A. M., Hakonarson, Hakon“…Several studies from large cohorts have been performed to search for key SCZ network genes using different analytical approaches, such as differential expression tests, genome-wide association study (GWAS), copy number variations, and differential methylations, or from the analysis of mutations residing in the coding regions of the genome. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196264por Cheung, Teris, Ho, Yuen Shan, Yeung, Jerry Wing-Fai, Leung, Sau Fong, Fong, Kenneth N. K., Fong, Tommy, Kranz, Georg S., Beisteiner, Roland, Cheng, Calvin Pak Wing“…Missing data were managed by multiple mutations. The level of significance will be set to p < 0.05. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196265por Wei, Cheng, Wang, Bo, Peng, Dazhao, Zhang, Xiaoyang, Li, Zesheng, Luo, Lin, He, Yingjie, Liang, Hao, Du, Xuezhi, Li, Shenghui, Zhang, Shu, Zhang, Zhenyu, Han, Lei, Zhang, Jianning“…Genetic alterations including duplications and deep mutations of the ALKBH5 gene were identified in several cancer types. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196266por Garciaz, Sylvain, Hospital, Marie-Anne, Alary, Anne-Sophie, Saillard, Colombe, Hicheri, Yosr, Mohty, Bilal, Rey, Jérôme, D’Incan, Evelyne, Charbonnier, Aude, Villetard, Ferdinand, Maisano, Valerio, Lombardi, Laura, Ittel, Antoine, Mozziconacci, Marie-Joelle, Gelsi-Boyer, Véronique, Vey, Norbert“…ASXL1, IDH and SFSR2 mutations were associated with a trend in a higher response rate in the R/R group. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196267por Gargallo, Pablo, Molero, Merche, Bilbao, Cristina, Stuckey, Ruth, Carrillo-Cruz, Estrella, Hermosín, Lourdes, Pérez-López, Olga, Jiménez-Velasco, Antonio, Soria, Elena, Lázaro, Marián, Carbonell, Paula, Yáñez, Yania, Gómez, Iria, Izquierdo-García, Marta, Valero-García, Jennifer, Ruiz, Carlos, Such, Esperanza, Calabria, Inés“…Clinically relevant mutations were detected in 94% of all patients. An analysis of the correlation between the genetic risk classification of AML (according to ELN 2017) established by the hospitals and that obtained by the Haematology OncoKitDx panel showed an almost perfect correlation (K = 0.94). …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196268por Buccisano, Francesco, Palmieri, Raffaele, Piciocchi, Alfonso, Arena, Valentina, Candoni, Anna, Melillo, Lorella, Calafiore, Valeria, Cairoli, Roberto, de Fabritiis, Paolo, Storti, Gabriella, Salutari, Prassede, Lanza, Francesco, Martinelli, Giovanni, Luppi, Mario, Capria, Saveria, Maurillo, Luca, Del Principe, Maria Ilaria, Paterno, Giovangiacinto, Irno Consalvo, Maria Antonietta, Ottone, Tiziana, Lavorgna, Serena, Voso, Maria Teresa, Fazi, Paola, Vignetti, Marco, Arcese, William, Venditti, Adriano“…The 2017 version of the European LeukemiaNet (ELN) recommendations, by integrating cytogenetics and mutational status of specific genes, divides patients with acute myeloid leukemia into 3 prognostically distinct risk categories: favorable (ELN2017-FR), intermediate (ELN2017-IR), and adverse (ELN2017-AR). …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196269por Maiorano, Brigida Anna, Maiorano, Mauro Francesco Pio, Cormio, Gennaro, Maglione, Annamaria, Lorusso, Domenica, Maiello, Evaristo“…PD-L1 cannot predict ICI response, whereas other biomarkers such as MSI and tumor mutational burden seem more accurate. Ongoing randomized trials will further clarify the role of these therapeutic options. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196270por Foster, Brittni M., Shi, Lihong, Harris, Koran S., Patel, Chirayu, Surratt, Victoria E., Langsten, Kendall L., Kerr, Bethany A.“…Thus, targeting the SCF/CD117 signaling axis with tyrosine kinase inhibitors could affect primary prostate carcinomas or play a role in reducing bone metastasis dependent on the gene deletions or mutations driving the patients’ prostate cancer.…”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196271por Li, Siming, Wu, Xiaowen, Yan, Xieqiao, Zhou, Li, Chi, Zhihong, Si, Lu, Cui, Chuanliang, Tang, Bixia, Mao, Lili, Lian, Bin, Wang, Xuan, Bai, Xue, Dai, Jie, Kong, Yan, Tang, Xiongwen, Feng, Hui, Yao, Sheng, Flaherty, Keith T, Guo, Jun, Sheng, Xinan“…Tumor programmed cell death ligand-1 (PD-L1) expression, tumor mutational burden (TMB), and gene expression profile (GEP) by messenger RNA sequencing were evaluated for correlation with survival. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196272por Yao, Ninghua, Zuo, Ling, Yan, Xiaodi, Qian, Jing, Sun, Jie, Xu, Huawei, Zheng, Feifei, Efird, Jimmy T., Kawagoe, Izumi, Wang, Yan, Ni, Sujie“…Gene set enrichment analysis (GSEA) showed that the high-risk group was associated with pro-tumor pathways and high-frequency mutations in TP53 were present in both groups. Single sample gene set enrichment analysis (ssGSEA) showed significant differences in immune cell infiltration subtypes and corresponding functions between the two groups. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196273por Wang, Jiachen, Shen, Kefeng, Mu, Wei, Li, Weigang, Zhang, Meilan, Zhang, Wei, Li, Zhe, Ge, Tong, Zhu, Zhoujie, Zhang, Shangkun, Chen, Caixia, Xing, Shugang, Zhu, Li, Chen, Liting, Wang, Na, Huang, Liang, Li, Dengju, Xiao, Min, Zhou, Jianfeng“…Heterozygous germline UNC13D mutations had the highest intergroup differences (26.9% vs. 0%; p=0.008). …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196274por O Murchu, Eamon, Marshall, Liam, Teljeur, Conor, Harrington, Patricia, Hayes, Catherine, Moran, Patrick, Ryan, Mairin“…PrEP was found to be safe, but unrecognised HIV at enrolment increased the risk of viral drug resistance mutations. Evidence for behaviour change or an increase in sexually transmitted infections was not found. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196275por Ni, Shujuan, Wang, Xin, Chang, Jinjia, Sun, Hui, Weng, Weiwei, Wang, Xu, Tan, Cong, Zhang, Meng, Wang, Lei, Huang, Zhaohui, Huang, Dan, Xu, Midie, Sheng, Weiqi“…Furthermore, the HER2 protein expression was significantly negatively correlated with RAS/BRAF mutations according to the HERACLES criteria. CONCLUSION: To our knowledge, this is the largest study of HER2 status in Asian patients with CRC. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196276por Chinigò, Giorgia, Grolez, Guillaume P., Audero, Madelaine, Bokhobza, Alexandre, Bernardini, Michela, Cicero, Julien, Toillon, Robert-Alain, Bailleul, Quentin, Visentin, Luca, Ruffinatti, Federico Alessandro, Brysbaert, Guillaume, Lensink, Marc F., De Ruyck, Jerome, Cantelmo, Anna Rita, Fiorio Pla, Alessandra, Gkika, Dimitra“…Molecular modeling analysis allowed the identification of four putative residues involved in TRPM8-Rap1A interaction. Point mutations of these sites impaired PPI as shown by GST-pull-down, co-immunoprecipitation, and PLA experiments and revealed their key functional role in the adhesion and migration of PC3 prostate cancer cells. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196277por Carlino, Francesca, Diana, Anna, Piccolo, Antonio, Ventriglia, Anna, Bruno, Vincenzo, De Santo, Irene, Letizia, Ortensio, De Vita, Ferdinando, Daniele, Bruno, Ciardiello, Fortunato, Orditura, Michele“…Through the characterization of the tumor microenvironment (TME), the analysis of peripheral blood and the evaluation of immune gene signatures, novel potential biomarkers have been explored, such as the Tumor Mutational Burden (TMB), Microsatellite Instability/Mismatch Repair Deficiency (MSI/dMMR) status, genomic and epigenomic alterations and tumor-infiltrating lymphocytes (TILs). …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196278por Socorro, Mairobys, Hoskere, Priyanka, Roberts, Catherine, Lukashova, Lyudmila, Verdelis, Kostas, Beniash, Elia, Napierala, Dobrawa“…This rare inherited skeletal dysplasia is caused by mutations in the TRPS1 gene coding for the TRPS1 transcription factor. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196279por Ahmed, Warish, Bivins, Aaron, Metcalfe, Suzanne, Smith, Wendy J.M., Ziels, Ryan, Korajkic, Asja, McMinn, Brian, Graber, Tyson E., Simpson, Stuart L.“…In particular, reverse transcription-quantitative PCR (RT-qPCR) has been used to detect and quantify SARS-CoV-2 RNA in wastewater, while monitoring viral genome mutations requires separate approaches such as deep sequencing. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
196280por Levitis, Elizabeth, Vogel, Jacob W, Funck, Thomas, Hachinski, Vladimir, Gauthier, Serge, Vöglein, Jonathan, Levin, Johannes, Gordon, Brian A, Benzinger, Tammie, Iturria-Medina, Yasser, Evans, Alan C“…Amyloid-beta deposition is one of the hallmark pathologies in both sporadic Alzheimer’s disease and autosomal-dominant Alzheimer’s disease, the latter of which is caused by mutations in genes involved in amyloid-beta processing. …”
Publicado 2022
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto