• Thumbnail for TREX1
    prime repair exonuclease 1 is an enzyme that in humans is encoded by the TREX1 gene. This gene encodes the major 3'->5' DNA exonuclease in human cells...
    14 KB (1,425 words) - 22:34, 9 December 2024
  • Thumbnail for Aicardi–Goutières syndrome
    of different genes, of which nine have been identified to date, namely: TREX1, RNASEH2A, RNASEH2B, RNASEH2C (which together encode the ribonuclease H2...
    30 KB (3,342 words) - 11:26, 22 August 2024
  • Thumbnail for Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
    C-terminal region of the TREX1 gene. This disease is associated witih DNA damage (chromosome damage) caused by a toxic mutant TREX1 protein, which causes...
    17 KB (1,801 words) - 06:00, 24 June 2024
  • for XML), a subset of Regular Language description for XML The proteins TREX1 and TREX2 T. rex (disambiguation) This disambiguation page lists articles...
    546 bytes (101 words) - 15:23, 19 December 2024
  • vasoconstriction or microvascular injury brought on by cold. A missense mutation in TREX1, encoding the 3′–5′ repair exonuclease 1, was found in affected individuals...
    15 KB (1,470 words) - 05:07, 9 August 2024
  • Aicardi–Goutières syndrome, a hereditary disease caused by mutations in the TREX1, RNASEH2B, RNASEH2C, RNASEH2A, ADAR1, SAMHD1, IFIH1, LSM11, or RNU7-1 gene...
    16 KB (1,614 words) - 17:54, 27 November 2024
  • 1:30,000-50,000 ADULT syndrome TP63 dominant Aicardi–Goutières syndrome TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, IFIH1 1:19,500,000 Albinism...
    43 KB (995 words) - 00:47, 12 December 2024
  • Thumbnail for Lupus
    2024 were classified as inborn errors of immunity genes, i.e., DNASE1L3, TREX1, IFIH1, Tartrate-resistant acid phosphatase and PRKCD and 28 other genes...
    136 KB (14,834 words) - 21:34, 20 December 2024
  • active L1 genomic retroelements by the three prime repair exonuclease 1 (TREX1) and excision repair cross complementing 1(ERCC) appear to mimic the action...
    55 KB (5,853 words) - 02:46, 17 December 2024
  • Aicardi–Goutières syndrome (AGS). Mutations in the 3’ repair exonuclease, TREX1, cause endogenous retroelements to accumulate in the cytosol, which can...
    23 KB (2,886 words) - 15:56, 23 September 2024
  • Thumbnail for Symptoms of COVID-19
    disease or during convalescence. Certain genetic polymorphisms (in the TREX1 gene) have been linked to susceptibility towards developing COVID-toe. A...
    57 KB (6,600 words) - 03:39, 9 December 2024
  • Thumbnail for Ribonuclease H
    type I interferon. AGS can also be caused by mutations in other genes: TREX1, SAMHD1, ADAR, and MDA5/IFIH1, all of which are involved in nucleic acid...
    54 KB (5,823 words) - 20:53, 22 July 2024
  • deposition). Familial Mediterranean fever Aicardi–Goutières syndrome with TREX1, SAMHD1 or IFIH1 mutations Spondyloenchondro-dysplasia with immune dysregulation...
    19 KB (1,836 words) - 09:52, 5 July 2024
  • active L1 genomic retroelements by the three prime repair exonuclease 1 (TREX1) and excision repair cross complementing 1 (ERCC) appear to mimic the action...
    20 KB (2,668 words) - 02:28, 20 June 2024
  • Thumbnail for TREX2
    Mazur DJ, Perrino FW (Aug 1999). "Identification and expression of the TREX1 and TREX2 cDNA sequences encoding mammalian 3'-->5' exonucleases". J Biol...
    9 KB (1,146 words) - 07:58, 28 October 2024
  • Thumbnail for Tomas Lindahl
    092448. PMID 15568983. Yang, Y. G.; Lindahl, T; Barnes, D. E. (2007). "Trex1 exonuclease degrades ssDNA to prevent chronic checkpoint activation and...
    16 KB (1,308 words) - 08:15, 18 September 2024
  • domain that carries out the 3’→5’ exonuclease and proofreading function. TREX1, the major 3'→5' exonuclease in humans, was initially called DNase III because...
    11 KB (1,473 words) - 02:27, 2 October 2024
  • Thumbnail for Abscopal effect
    2015;75:2232-2242. Vanpouille-Box C, Alard A, Aryankalayil MJ, et al. DNA exonuclease Trex1 regulates radiotherapy-induced tumour immunogenicity. Nat Commun. 2017 Jun...
    9 KB (1,126 words) - 01:12, 21 August 2024
  • are classified as inborn errors of immunity genes, i.e., the DNASE1L3, TREX1, IFIH1, Tartrate-resistant acid phosphatase, and PRKCD genes and 29 other...
    84 KB (10,377 words) - 00:47, 3 December 2024
  • Q5T2D2 17336 TREML4 HGNC:30807 Q6UXN2 17337 TRERF1 HGNC:18273 Q96PN7 17338 TREX1 HGNC:12269 Q9NSU2 17339 TREX2 HGNC:12270 Q9BQ50 17340 TRG HGNC:12271 [3]...
    242 KB (17 words) - 18:43, 6 October 2024
  • Thumbnail for TFEB
    Juvenile Batten disease and Sanfilippo syndrome type B. TFEB is activated in Trex1-deficient cells via inhibition of mTORC1 activity, resulting in an expanded...
    18 KB (2,233 words) - 11:48, 16 January 2024
  • Activation of Innate Immunity Depends Strongly on the Intracellular Level of TREX1 and Sensing of Incomplete Reverse Transcription Products". Journal of Virology...
    10 KB (974 words) - 10:10, 20 May 2024
  • 218000; SLC12A6 Aicardi–Goutières syndrome 1, dominant and recessive; 225750; TREX1 Aicardi–Goutières syndrome 2; 610181; RNASEH2B Aicardi–Goutières syndrome...
    234 KB (18,877 words) - 06:16, 6 November 2024