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10,281 Possible Causes for PGBD3, gene

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  • Premature Ovarian Failure

    Five genes were selected for analysis, including 10 common gene polymorphisms [BMP15 (-9C G, 788insTCT and 852C T), ESR1 (-351A G and -397C T), FMR1 CGG repeat, FSHR (919A[ncbi.nlm.nih.gov] The localization of the CSB-PGBD3 fusion protein to UVA-induced nuclear DNA repair foci further suggests that the CSB-PGBD3 fusion protein, like many other proteins that can[ncbi.nlm.nih.gov] It also possesses a critical role in the germ cell maintenance, and loss of HELQ gene leads to subfertility.[ncbi.nlm.nih.gov]

  • Cockayne Syndrome

    Transcriptome analysis of human fibroblasts revealed that even in the absence of DNA damage, CSB affects the expression of thousands of genes, many of which are neuronal genes[ncbi.nlm.nih.gov] As a result, primate CSB genes now generate both CSB protein and a conserved CSB-PGBD3 fusion protein in which the first 5 exons of CSB are alternatively spliced to the PGBD3[ncbi.nlm.nih.gov] Use of these SSOs induced a frame shift in order to generate an alternative stop codon at the upstream region of the PGBD3 invasion site.[ncbi.nlm.nih.gov]

  • Acute Gastroenteritis

    Phylogenetic analysis of nucleotide sequences classified GCR strains of the study in to I2 genotype of the VP6 gene.[ncbi.nlm.nih.gov] Within the strains nucleotide/amino acid divergence of 0.1-3.4%/0.0-4.1% was noted in all the RVA structural and non-structural genes.[ncbi.nlm.nih.gov] Child-parent associations were found for bacterial pathogenicity genes, viruses, G. lamblia and D. fragilis.[ncbi.nlm.nih.gov]

    Missing: PGBD3
  • Urinary Tract Infection

    We report here that UPEC upregulates the expression of ethanolamine utilization genes during uncomplicated UTIs in humans.[ncbi.nlm.nih.gov] The gene frequency of genes was determined using PCR, and analyzed using SPSS version 21 software.[ncbi.nlm.nih.gov] Maybe that yet unknown gene polymorphisms together with geographical and /or socio-economic differences can influence on the development of RS.[ncbi.nlm.nih.gov]

    Missing: PGBD3
  • Insect Bite

    Immunophenotyping, direct immunofluorescence (DIF) tests, and IgH gene rearrangement studies were performed in the lesions associated with MCL only.[ncbi.nlm.nih.gov] […] insensitive to permethrin is discussed along with the surprising contrary clinical evidence from Europe about efficacy of permethrin in children with head lice carrying kdr-like gene[ncbi.nlm.nih.gov]

    Missing: PGBD3
  • Influenza

    […] triple-reassortant influenza A virus with a HA that resembles H3 of human seasonal influenza from 2004 to 2005, N2 from influenza A virus already established in swine, and the internal gene[ncbi.nlm.nih.gov] We detected six reassortants with gene segments derived from human H1N1/H1N1pdm09 and various human H3N2 viruses that circulated during various periods since 1968.[ncbi.nlm.nih.gov] WGS confirmed clustered transmission of two genetically different influenza A(H1N1)pdm09 strains initially identified by analysis of HA and NA genes.[ncbi.nlm.nih.gov]

    Missing: PGBD3
  • Skin Infection

    There was also increased expression of genes encoding virulence factors, namely secreted toxins and fibronectin and/or fibrinogen-binding proteins.[ncbi.nlm.nih.gov] Leukocyte adhesion deficiency (LAD) I is a well-described genetic disorder in which leukocytes are unable to migrate to sites of inflammation due to mutations in the ITGB2 gene[ncbi.nlm.nih.gov] The VZV genome has at least 70 known or predicted open reading frames (ORFs), but understanding how these gene products function in virulence is difficult because VZV is a[ncbi.nlm.nih.gov]

    Missing: PGBD3
  • Acute Bronchitis

    Studies have reported gene-by-environment interaction for chronic respiratory conditions but none on acute illnesses in children.[ncbi.nlm.nih.gov] […] pneumoniae and the 16S rRNA gene of C . pneumoniae [ 19 ].[journals.plos.org] Air pollution and childhood bronchitis: Interaction with xenobiotic, immune regulatory and DNA repair genes. Environ Int . 2016 Feb. 87:94-100. [Medline] .[emedicine.medscape.com]

    Missing: PGBD3
  • UV-Sensitive Syndrome

    UV damage, is located on chromosome 10, we sequenced the CSB gene from UVs1KO and detected a homozygous null mutation.[ncbi.nlm.nih.gov] 7 protein N-terminus binding GO:0047485 9.65 ERCC2 ERCC3 ERCC5 ERCC6 PGBD3 8 protein C-terminus binding GO:0008022 9.63 ERCC2 ERCC3 ERCC6 PGBD3 RAD51 USP7 9 insulin-like[malacards.org] [from OMIM ] Genes See tests for all associated and related genes Associated genes Help Also known as: ARMD5, CKN2, COFS, COFS1, CSB, CSB-PGBD3, POF11, RAD26, UVSS1, ERCC6[ncbi.nlm.nih.gov]

  • Pharyngitis

    The molecular investigation of biofilm-associated genes revealed that 84.13% (n 53) of isolates were found positive for icaADBC genes.[ncbi.nlm.nih.gov] The group A streptococcus (GAS) M protein, encoded by the emm gene, acts as a major virulence factor.[ncbi.nlm.nih.gov] […] mutations with a possible functional effect on the inflammasomes (MEFV E148Q and NLRP3 Q703K) have been found in several PFAPA cohorts, the role of inflammasome-related genes[ncbi.nlm.nih.gov]

    Missing: PGBD3

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