284) predicted methylation of several HPA axis genes, including novel gene associations w |
285) the intestinal expression profiles of the genes related to drug absorption, distribu |
286) ddition, the increased mRNA expression of genes related to fatty acid oxidation and |
287) They pave the way to identify genes related to important symbiotic trait |
288) dulated the expression of six clusters of genes related to structural constituents o |
289) med that hsfA regulates the expression of genes related to the HS response, cell wal |
290) h mTORC1 signalling and the expression of genes related to the metabolism of glucose |
291) STAT3, a transcription factor of several genes related to tumorigenesis, is activat |
292) CA+vehicle) altered the expression of 667 genes at 2-day and 187 genes at 2-week tim |
293) enes: 113 and 75 differentially expressed genes at 2-day and 2-week timepoint, respe |
294) CA+vehicle) differentially regulated 4061 genes at 2-day and 3169 genes at 2-week ti |
295) A (MS4A) and bridging integrator 1 (BIN1) genes at genome-wide significance that wer |
296) analyses show that 79.1% of the proximal genes at these loci and 76.2% of the genes |
297) AD and related disorders to validate the genes at these significant loci. |
298) Among candidate genes for GGE, a significant association w |
299) precipitation (HiChIP) to identify target genes for PrCa GWAS risk loci. |
300) enrichment among known complement system genes for SCZ. |
301) effect of MLR-1023 on the upregulation of genes for energy expenditure and insulin s |
302) l as identification of natural suppressor genes for neurodegenerative diseases. |
303) te subtype-specific vulnerability partner genes for the genetic drivers of individua |
304) only modulates the expression of specific genes but also has ripple effects on trans |
305) al-encoded electron transport chain (ETC) genes but not nuclear-encoded mitochondria |
306) result of not only activity of individual genes, but also gene-environment and gene- |
307) found in expression of about half of the genes, but in general the differences were |
308) ntification of a number of NDD-associated genes, but reports of cognitive and develo |
309) lity SNPs can interact with cancer driver genes to affect cancer progression and ide |
310) lity SNPs can interact with cancer driver genes to affect cancer progression and pre |
311) are distinct from symptoms and which link genes to manifest illness. |
312) (eQTLs) corresponding to tissue-specific genes to prioritize a relevant tissue unde |
313) Our results identified promising genes to pursue in functional studies to b |
314) n effect on 28 other outcomes, as well as genes which may have a more specific role |
315) ll clusters with differentially expressed genes which represent distinct neuronal an |
316) receptor (TLR) and interleukin-1 receptor genes, which are integral to cellular inna |
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