339) a change in 119 differentially expressed genes (DEGs) between mThy1-Asyn mice and w |
340) networks of the differentially expressed genes (DEGs) were built by the Search Tool |
341) luated the impact of human IFN-stimulated genes (ISGs) on viral replication. |
342) ntly, enrichment of interferon-stimulated genes (ISGs) predicted a favorable respons |
343) Type 1 interferon response genes (ISGs) were among those that were di |
344) germline variants in cancer-predisposing genes among 15 children with SMNs after ch |
345) ects to identify differentially expressed genes among PTSD cases and controls. |
346) The differentially expressed genes among the three groups were analyzed |
347) ium tuberculosis (Mtb) EmbR, and EmbC/A/B genes cause EMB resistance. |
348) Rare pathogenic variants in sarcomere genes cause HCM, but with unexplained phen |
349) therapeutic targets, mutations in 55 GPCR genes cause about 66 inherited monogenic d |
350) s associated loci, which are enriched for genes expressed in growth plate chondrocyt |
351) control metabolism through regulation of genes expressed in the brain, or that cont |
352) owever, it remains unclear which specific genes expressed in which layers of the gro |
353) ts show that interactions between SNPs in genes from the aging pathways influence su |
354) ne coexpression networks based on the hub genes from the candidate modules were then |
355) We selected candidate genes from well-known aging pathways (IGF1 |
356) that CCR2, LMO7, STEAP4, NNAT, and TCF7L2 genes had good diagnostic performance for |
357) th male mice, and 26 of the 35 BA-related genes had marked gender difference in mice |
358) Almost all identified genes had not previously been implicated i |
359) only a small number of disease-associated genes have been identified. |
360) nknown significance" (VUS) in transporter genes have not been characterized. |
361) 246 AD risk genes have not been identified as AD risk |
362) G pathway enrichment reanalysis of the 21 genes identified five key genes (CCNB1, BU |
363) in ten emerging recurrent NDD-associated genes identified from large scale sequenci |
364) a confirm previously reported PrCa target genes identified through GWAS/eQTL overlap |
365) howing cannabis-associated alterations at genes important for early development. |
366) e transcriptional network, normalizes the genes important for hepatocyte function, a |
367) network and normalizes the expression of genes important for hepatocyte function, i |
368) regulate expression of the corresponding genes through CRISPR interference (CRISPRi |
369) rogen receptor-coregulatory and essential genes through mRNA 3' UTR sequence complem |
370) edge about Mendelian phenotypes and their genes through the years. |
371) lead to the suppression of cilia-related genes while also inducing nucleolin. |
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