363) nting at 2.5 years old would predict HPA gene DNA methylation similarly to abuse an |
364) Only one gene, HDAC8, could explain the phenotype i |
365) ased expression of prosurvival p53 target gene KITLG and attenuation of p53-mediated |
366) s the expression of its downstream target gene NUAK2. |
367) yclopedia of Genes and Genomes (KEGG) and Gene Ontology (GO) enrichment analyses of |
368) flavin-containing monooxygenase encoding gene OsYUC11 as a key contributor to auxin |
369) In particular, a telomere maintenance gene, POT1, was recurrently mis-spliced by |
370) osterone levels and glucocorticoid target gene, Redd1, in muscle. |
371) isolate only contains one copy of the vhp gene, S. |
372) in the promoter region (5-HTTLPR) of the gene SLC6A4. |
373) One example is the sweet taste receptor gene Tas1r2 Previous analysis of partial s |
374) The International Society for Cell & Gene Therapy mesenchymal stromal cell (MSC |
375) Microbiome analysis with 16S rRNA gene V4 sequencing showed that the gut mic |
376) locus spans 214 kb, and contains 112 TRBV genes, a single TRBD gene, 31 TRBJ genes a |
377) ts, other subjects at risk are carries of gene abnormalities codifying for ion chann |
378) and 17,610 matched controls, the PHGDH gene achieves genome-wide significance (P |
379) Epigenetic regulation-control of gene action through chemical and structura |
380) PEI-pVEGF might be a potential 3D printed gene activated scaffold for bone regenerat |
381) oreover, ZKSCAN3, a repressor of lysosome gene activation by TFEB, was amplified by |
382) lls (GCs) and surprisingly found that the gene-regulation activity of androgen recep |
383) otective variant, rs955263, in the SORBS2 gene against both Maf and Mtb infections ( |
384) d composition with environmental 16S rRNA gene amplicon sequencing. |
385) Using gene-set analyses, we found the genes that |
386) In addition, the complete catfish TR gene annotation was used to compile a TR g |
387) data were analyzed using both a candidate gene approach that targeted variants in ba |
388) The gene arrangement and content are consisten |
389) ompared to a pregnane X receptor reporter gene assay. |
390) oped R package 'snpsettest', we performed gene-based association tests and identifie |
391) f several HPA axis genes, including novel gene associations with AVPRB1, CRHR1, CRHR |
392) s obtaining allelic counts within defined gene/region boundaries are unavailable or |
393) These gene by nutrient interactions affect the l |
394) Using MSN-PEG as a gene carrier, the plasmids were successful |
395) Blood gene-expression changes within individuals |
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