301) rn a C-terminally tagged copy of the PF16 gene to the original locus, which resulted |
302) France Genomics and Ethics Network (UK-FR GENE), which has been set up to reflect on |
303) ing to the formation of the fused EWSFLI1 gene, which codes for an aberrant transcri |
304) entified a copy of IS6110 within the moaX gene, which turned out to be specific for |
305) Gene-ontology analysis revealed the role o |
306) lly relevant populations, undetectable by gene-expression analysis. |
307) Mutations in the ABCA4 gene are a common cause of Stargardt disea |
308) or SK4 channels and encoded by the KCNN4 gene, are activated by a rise of the intra |
309) paRG did not activate PXR in the reporter gene assay, illustrating the limitations o |
310) ) HepaRG cells, as well as a PXR reporter gene assay, were used to investigate the m |
311) All those who took part had changes in a gene called ALK, which is involved in cell |
312) a certain resistance mutation in the EGFR gene, called T790M. |
313) Paralogs of the Obp50 gene cluster are expressed in metabolic an |
314) 3 (rs10735079, P = 1.65 × 10-8) in a gene cluster that encodes antiviral restri |
315) As expected, MSN-PEG possessed excellent gene delivery capacity with good binding, |
316) Among the current gene delivery carriers, cell-derived extra |
317) h after transfection, luciferase reporter gene detection kit was used to detect the |
318) rase were detected by luciferase reporter gene detection kit, and the ratio of the t |
319) role of RNA modifications in fine-tuning gene expressions at several levels has bee |
320) RNAs (lncRNAs), have been ascertained in gene expressions. |
321) e (HSC-3) with homozygous deletion of the gene for cathepsin S (CTSS) with CRISPR/Ca |
322) and brain-targeted delivery of the pApoE2 gene for effective AD therapy. |
323) th DAC induced the conversion of the FBW7 gene from a methylated form to an unmethyl |
324) mers to amplify the Acanthamoeba 18S-rRNA gene from mouse ocular tissue. |
325) n, allele variants of GPCRs, pseudogenes, gene fusion, and gene dosage, contribute t |
326) f GPCRs, uniparental disomy, pseudogenes, gene fusion, and gene dosage, need to be e |
327) Genetic variants in the SLCO1B1 gene have been associated with altered pro |
328) binding protein C (encoded by the MYBPC3 gene) have been associated with hypertroph |
329) oss of function in both copies of the RB1 gene is the causal mutation of retinoblast |
330) The SorLA protein, encoded by the SORL1 gene, is a major player in Alzheimer's dis |
331) erature and used GeneMANIA to investigate gene ontologies and predicted protein-inte |
332) Pathway analysis identified 15 gene ontologies that were differentially a |
333) nd lentiviral vector therapy to deliver a gene or secretory protein); 2. |
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