378) PCs and predicts differentially expressed genes between the two lineages. |
379) in obese children, and differences in VF genes between these two cohorts. |
380) years, acquire new antibiotic resistance genes by horizontal gene transfer, and ini |
381) ng pathway, which reduces hepatic gluconeogenesis by inhibiting the gene expression |
382) expression level of IL-1β and MCP-1, two genes contributing to MMPs expression. |
383) he master regulator for the expression of genes contributing to the bacterial infect |
384) Trait Loci hotspot for a wider network of genes enriched for SCFD1 function and Amyo |
385) e associated with a block of co-expressed genes enriched for adaptive immune, histon |
386) o turn different carbohydrate utilization genes on and off in response to changing n |
387) xport factor) as candidate CDH-associated genes on the basis of de novo variants at |
388) Significantly, genes regulated by both formoterol and bud |
389) qPCR data showed that several genes regulated by isocitrate dehydrogenas |
390) rategy aimed at identifying non-essential genes required by tumour cells to sustain |
391) The genes required for K-antigen capsule synth |
392) Bacteroides have many genes responsible for breaking down differ |
393) ltures, with messenger RNA expression for genes responsible for key hepatic function |
394) hylene biosynthesis and signaling-related genes than B-385. |
395) of bivalent programming of developmental genes than that found between human and no |
396) duct of one of the putative antibacterial genes, the N. |
397) f CKD are SNPs in the MYH9/APOL1 and UMOD genes, the proteomic CKD273 biomarker pane |
398) ring time in Arabidopsis In this issue of Genes & Development, Zhao and colleagu |
399) eam genes, so-called cooperation response genes (CRGs). |
400) an expression pattern of immediate early genes (IEG) in the mouse somatosensory cor |
401) d not reduce the number of flow-sensitive genes (LCA+statin versus RCA+statin) compa |
402) incosamide-streptogramin (MLS) resistance genes (P = 0.037) increased after trea |
403) eviously unreported significantly mutated genes (SMGs) (including MSN, GPX1, SPRED3, |
404) nucleotide (CDN) stimulator of interferon genes (STING) agonists and Mn2+. |
405) ic activation of stimulator of interferon genes (STING), a PRR highly expressed in P |
406) ng sequences of both sweet taste receptor genes (Tas1r2 and Tas1r3) in 34 representa |
407) Lastly, we identified four genes (UBA7, HLA-F, HSPA1B, and RERE) with |
408) receptors (TLR-2/4) and tight junctional genes (ZO-1, occludin, claudin-1) along wi |
409) Then a ratio of two B cell informative genes (a target gene and a stably expresse |
410) re of Drosophila stimulator of interferon genes (dSTING) in complex with 3'2'-cGAMP |
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