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 |
396) urated content in CTD, including chemical-gene, chemical-phenotype, and chemical-dis |
397) Gene-edited clones were identified by quan |
398) es2 is similar to human CES2A-CES3A-CES4A gene cluster, with highly similar gene str |
399) o-occurrence network analysis detected VF gene clusters closely related to host infl |
400) n Black and White HKCs, modulation of the gene, coding for an enzyme involved in sex |
401) ese cohort-specific clusters varied in VF gene combinations and cascade reactions af |
402) The data show that deletion of the PG0720 gene confers a defect in the presentation |
403) In the dense space of gene connectivity, TopNet reveals a sparse |
404) ndividuals and identified LONP1 as a risk gene contributing to CDH through both de n |
405) erential expression analysis and weighted gene correlation network analysis (WGCNA) |
406) t these particular mutations in the ABCA4 gene could be associated with a specific d |
407) h has the smiA (sensitive to miltefosine) gene deleted, conferring a phenotype of su |
408) iants (SNVs) and one linking recurrent HP gene deletion and cholesterol levels (p = |
409) als for applications like controlled drug/gene/protein delivery, biosensors, and art |
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