230) ecific to the cancer subtype in which the gene was predicted to be specifically leth |
231) d 25 BRD samples were downloaded from the Gene Expression Omnibus (GEO) and then ana |
232) croarray datasets were retrieved from the Gene Expression Omnibus (GEO) database. |
233) onal Center for Biotechnology Information Gene Expression Omnibus Database of Americ |
234) ancer Genome Atlas (TCGA) program and the Gene Expression Omnibus for comparisons. |
235) analyzed by the Kaplan-Meier Plotter and Gene Expression Profiling Interactive Anal |
236) nd pressing concerns include detection of gene drive alleles with non-functional eff |
237) frequency of sampling in order to detect gene drive alleles, drive-resistant allele |
238) As gene drive mosquito projects advance from |
239) We explore these monitoring needs for gene drive mosquito projects progressing t |
240) f particular importance for non-localized gene drive projects, as the potential scal |
241) CRISPR/Cas9 gene editing in iPSC lines often has a low |
242) In addition to gene editing in the treatment of genetic d |
243) presented here indicate that CRISPR/Cas9 gene editing of a suboptimal exon 19/intro |
244) We analyzed the effects of gene editing of this cluster on organismal |
245) ated (Cas) protein system, as an emerging gene editing system, can be divided into c |
246) 2 cancer patients to jointly characterize gene mutations (n = 14,789) and mCAs ( |
247) should be considered in conjunction with gene mutations in the surveillance of pati |
248) Since Kir channel gene mutations may alter neuronal excitabi |
249) tions, most CH studies have characterized gene mutations or mosaic chromosomal alter |
250) ury, and de novo PRKD1 (protein kinase D1 gene) mutations have been identified in pa |
251) nd type Ⅰ collagen, fibrosis inhibiting gene of TGF-β3, and mechanotransduction-r |
252) ells (HUMSCs) transfected with the IFN-γ gene of human (h)/mice (m) (HUMSCs + Ad- |
253) utonomous manner to study the role of any gene of interest and its effect on CGN mor |
254) 11A1 and SORBS2 as a potential protective gene of substantial interest for TB, which |
255) Interestingly, Cyp2b10, a target gene of the nuclear receptor CAR, was also |
256) years, the functional roles for miRNAs in gene regulation have been well established |
257) nstrate a direct role of HSF1 in synaptic gene regulation that has important implica |
258) studies increase risk of disease through gene regulation via expression Quantitativ |
259) Epigenetic memory plays crucial roles in gene regulation. |
260) m corticosterone contributed to circadian gene regulation. |
261) terogeneous (HS) animals to map genes and gene networks associated with both behavio |
262) Our work has focused on the genes and gene networks associated with risk for exc |
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