335) , particularly one-carbon metabolites, on gene pathways and neurodevelopment. |
336) Expression differences in gene pathways related to the immune system |
337) and primary DPCs group; the variation of gene profile data of more than 90% of DPCs |
338) is diagnostically helpful as the mutated gene profile is shared between the convent |
339) ven Cre (dLckCre) in which the distal Lck gene promoter drives Cre expression in the |
340) ntributing to the activation of the grp78 gene promoter. |
341) Multi-gene sequencing identified a species of at |
342) The 16S rRNA V4 gene sequencing was performed in the feces |
343) SBA analysis identified three significant gene sets after Bonferroni correction, imp |
344) roach for BC development to detect shared gene sets in enriched subnetworks across B |
345) -protein induces nucleolin and suppresses gene transcripts specific to ciliated cell |
346) Deeper analyses revealed 382 gene transcripts varied by age and 315 var |
347) ood samples and the 17 exons of the TGFBI gene were amplified by PCR and sequenced b |
348) 0-64 CAG repeats) in the huntingtin (HTT) gene were found in three (0.12%) patients |
349) haplotype within the Fc gamma receptor 2C gene (FCGR2C) reduced the risk of HIV-1 ac |
350) al methods have been proposed for testing gene-environment (G-E) interactions under |
351) Variants in the Apolipoprotein L1 (APOL1) gene (G1-rs60910145, rs73885319, G2-rs7178 |
352) ous deletion of α-1-3-galactotransferase gene (GGTA1; GTKO) using the clustered reg |
353) scribed from its parental mGLUR4 receptor gene (GRM4) functions as a "molecular-spon |
354) Pharmacogenetic (PGx) literature has shown benefic |
355) iants in the voltage-gated sodium channel gene (SCN1A) are amongst the most common g |
356) ing the alveolar type 2 (AT2) cell marker gene (SFTPC) and the alveolar macrophage m |
357) is caused by dysfunctional maternal UBE3A gene (maternal 15q11-13 deletions, materna |
358) ) results from loss of a tumor suppressor gene - TSC1 or TSC2, encoding hamartin and |
359) d analyses, only two variants, one in the gene ATP-binding cassette transporter B1 ( |
360) GARCOM ("Gene And Region Count Of Mutations") libra |
361) nation of the third copy of chromosome 21 gene BACE2, but prevented by combined chem |
362) The fusion gene BCR‑ABL is an important biological |
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 |
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