Keyword Analysis & Research: cgggg

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Keyword CPC PCC Volume Score Length of keyword
cgggg1.450.57590355

Keyword Research: People who searched cgggg also searched

Keyword CPC PCC Volume Score
cgggg1.510.4274435
cggggh1.190.4321084
cggggf0.720.1707471
cggggv0.360.7272745
cggggff0.570.8522826
cggggc1.310.8876970
cggggy10.715072
cggggt1.320.6319338
cggggd1.030.3900111
gggghhhh0.860.2199897
cggggb0.180.270816
chegg1.050.8295624
cggggu1.59161618
cggggfd0.710.8720617
cgggghip0.10.240554

Search Results related to cgggg on Search Engine

  • CGGG - YouTube

    youtube.com

    https://www.youtube.com/channel/UCbjxYa1F_1Lbm-IA5yAgWxg

    WEBCGGG. @CGGG168 ‧. 8.04M subscribers ‧ 736 videos. facebook.com/cggg1tao and 2 more links. Home. Videos. Live. Playlists. Community. FREE FIRE คือ GMTH ได้ยินเสียง. …

    DA: 68 PA: 48 MOZ Rank: 92

  • Comprehensive evaluation of the genetic variants of interferon

    nih.gov

    https://pubmed.ncbi.nlm.nih.gov/18063667/

    WEBMar 15, 2008 · The CGGGG indel explains the association signal from multiple SNPs in the IRF5 gene, including rs2004640, rs10954213 and rs729302 previously considered to be causal variants in SLE. The CGGGG indel contains three or four repeats of the sequence CGGGG with the longer allele containing an additional SP1 binding site as the risk allele …

    DA: 53 PA: 82 MOZ Rank: 55

  • Genetic variants and disease-associated factors contribute to …

    nih.gov

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213692/

    WEBThe CGGGG indel explained the association signal from multiple SNPs in the IRF5 gene, including rs2004640 and rs10954213, previously considered to be causal variants in SLE (Fig. 1A). Here, we examine the functional association of the risk alleles of these four polymorphisms (CGGGG indel, rs2004640, rs10488631, and rs10954213) with IRF-5 ...

    DA: 28 PA: 77 MOZ Rank: 93

  • Genetics and epigenetics in primary Sjögren’s syndrome - PMC

    nih.gov

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121440/

    WEBMay 13, 2021 · This article reviews the hitherto published genetic studies and our current understanding of epigenetic mechanisms in pSS. Keywords: primary Sjögren’s syndrome, genetics, GWAS, HLA, IRF5, STAT4, epigenetics, DNA methylation, histone modification, non-coding RNA.

    DA: 2 PA: 65 MOZ Rank: 21

  • The CGGGG Insertion/Deletion Polymorphism of the

    wiley.com

    https://onlinelibrary.wiley.com/doi/pdf/10.1002/art.24662

    WEBThis study was undertaken to investigate whether a 5-bp (CGGGG insertion/deletion) promoter polymorphism is involved in genetic predisposition to primary Sjo ̈gren’s syndrome (SS) and to assess the functional consequences of this polymorphism. Methods.

    DA: 38 PA: 10 MOZ Rank: 84

  • The CGGGG insertion/deletion polymorphism of the

    wiley.com

    https://onlinelibrary.wiley.com/doi/10.1002/art.24662

    WEBJun 29, 2009 · Recently, a 5-bp insertion/deletion polymorphism (CGGGG insertion/deletion) located in the promoter region of the IRF5 transcript containing exon 1A was described, which may resolve this question. The IRF5 CGGGG insertion/deletion has been associated with ulcerative colitis, Crohn's disease ( 8 ), and lupus ( 6 ).

    DA: 99 PA: 42 MOZ Rank: 5

  • The CGGGG insertion/deletion polymorphism of the IRF5 …

    nih.gov

    https://pubmed.ncbi.nlm.nih.gov/19565491/

    WEBOur findings indicate an association of the CGGGG insertion/deletion polymorphism of the IRF5 promoter with primary SS. Patients carrying the 4R CGGGG IRF5 allele had a high level of mRNA for IRF5 in PBMCs and salivary gland epithelial cells, …

    DA: 93 PA: 25 MOZ Rank: 77

  • Entry - *607218 - INTERFERON REGULATORY FACTOR 5; …

    omim.org

    https://www.omim.org/entry/607218

    WEBSep 30, 2019 · PheneGene Graphics. TEXT. Description. Interferon regulatory factors (IRFs) are transcription factors that possess a novel helix-turn-helix DNA-binding motif and mediate virus- and interferon (IFN)-induced signaling pathways. Cloning and Expression.

    DA: 60 PA: 4 MOZ Rank: 8

  • Genetic Versus Non-genetic Drivers of SLE: Implications of

    springer.com

    https://link.springer.com/article/10.1007/s11926-019-0803-3

    WEBJan 15, 2019 · 850 Accesses. 8 Citations. Explore all metrics. Abstract. Purpose of Review. Systemic lupus erythematosus (SLE) is characterized by a breakdown of immune tolerance, resulting in inflammation and tissue destruction. While the primary causes of SLE are still obscure, the disorder is highly heritable.

    DA: 49 PA: 16 MOZ Rank: 28

  • Columbus Consolidated Government

    columbusga.gov

    https://www.columbusga.gov/Home/vm/portals=

    WEBCouncil District 9 at Large. 200 Spring Harbor Dr Columbus, Georgia 31904 706-587-8322 [email protected].

    DA: 47 PA: 43 MOZ Rank: 22