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18 Possible Causes for (S, RAD18, homolog

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  • Familial Congenital Mirror Movements 2

    S. Terry Canale, James H. Beaty, and 42 other authorities from the world-renowned Campbell Clinic.[books.google.com] The highly conserved RAD51 gene encodes a protein involved in DNA repair through the Homologous Recombination (HR) pathway.[cags.org.ae] DNA binding Related Protein POLR2G; OBFC2B; RAD51C; SSBP1; MCM4; ERCC4; C10orf2; PMS1; HNRNPK; WBP11 Function single-stranded DNA-dependent ATPase activity Related Protein RAD18[creativebiomart.net]

  • Werner Syndrome

    Genet. 62 , 25–30 (1982). 32 Samantray, S. K., Samantray, S., Johnson, S. C. & Bhaktaviziam, A. Aust. N.Z. J. Med. 7 , 309–311 (1977). 33 Sparkes, R. S. et al.[doi.org] Such homology does not necessarily mean that WRN encodes an active helicase.[ncbi.nlm.nih.gov] ., Tomilin, N. 2004 DNA damage-induced accumulation of Rad18 protein at stalled replication forks in mammalian cells involves upstream protein phosphorylation Biochem.[doi.org]

  • Fanconi Anemia

    Monoubiquitinated FANCD2 colocalizes with BRCA1 and RAD51 in S-phase-specific nuclear foci.[ncbi.nlm.nih.gov] […] in mutagenic non-homologous end joining (m-NHEJ) and increases in canonical NHEJ, which was independently confirmed by measuring V(D)J recombination.[ncbi.nlm.nih.gov] The E3 ubiquitin ligase RAD18 regulates ubiquitylation and chromatin loading of FANCD2 and FANCI.[ncbi.nlm.nih.gov]

  • Hepatitis B Virus

    […] corresponding region of the DHBV genome, a hypothetical protein which closely matches the hydrophilicity profile of X proteins can be predicted, despite limited sequence homology[ncbi.nlm.nih.gov] Characterization of a novel human SMC heterodimer homologous to the Schizosaccharomyces pombe Rad18/Spr18 complex . Mol. Biol. Cell 12 , 1583–1594 (2001) 40.[nature.com] According to the mutation type, five pre-S/S variants have been identified: pre-S deletion, pre-S point mutation, pre-S1 splice variant, C-terminus S point mutation, and pre-S[ncbi.nlm.nih.gov]

  • X-Linked Intellectual Disability Type Nascimento

    [Date last reviewed: 2016-06-23] Comments on ortholog(s) Ortholog of human genes UBE2A and UBE2B (1 Drosophila to 2 human).[flybase.org] […] ligase A; ubiquitin carrier protein A; ubiquitin conjugating enzyme E2A (RAD6 homolog); HR6A; ubiquitin-conjugating enzyme E2A (RAD6 homolog); wu:fa01h11; si:bz46j2.4; mp[creative-biogene.com] UBE2A cooperates with RAD18 to ubiquitinate PCNA in response to DNA damage [5] .[wikigenes.org]

  • Psoralen

    Together, our results demonstrate that hPso4 participates in cell proliferation and the maintenance of genome stability by regulating homologous recombination.[ncbi.nlm.nih.gov] Loss of REV3 function, in the error-prone branch, and of RAD5 and UBC13, in the error-free branch, produced moderate increases in deletions and triplications; rad18 cells,[ncbi.nlm.nih.gov] Identification of molecular biomarkers of PUVA sensitivity may facilitate treatment predictability.The glutathione S-transferases (GSTs) influence cutaneous defence against[ncbi.nlm.nih.gov]

  • Trypanosoma Brucei

    The ability of an ERK8 homolog to phosphorylate a PCNA homolog is a novel biochemical property that is first demonstrated here in T. brucei and may be unique to this pathogen[ncbi.nlm.nih.gov] Ramesh for isolation and sequence of Giardia Rad18 , to Robert B. Moore for partial T. vaginalis Spo11 sequence, to Justine M.[doi.org] In particular, elevated levels of metabolites involved in the metabolism of S-adenosyl-L-methionine, an essential methyl group donor, were found.[ncbi.nlm.nih.gov]

  • Ataxia Telangiectasia

    Enhancer of zeste homolog 2 (EZH2), a core catalytic component of PRC2, is a new ATM kinase target, and ATM-mediated phosphorylation of EZH2 on Ser734 reduces protein stability[ncbi.nlm.nih.gov] Kanu, T Zhang, R A Burrell, A Chakraborty, J Cronshaw, C DaCosta, E Grönroos, H N Pemberton, E Anderton, L Gonzalez, S Sabbioneda, H D Ulrich, C Swanton and A Behrens , RAD18[doi.org] Nat Genet. 2006; 38 :873–5. [ PubMed : 16832357 ] Sahama I, Sinclair K, Fiori S, Pannek K, Lavin M, Rose S.[ncbi.nlm.nih.gov]

  • Ruijs Aalfs Syndrome

    […] repair has been shown to be mediated by specific enzymes such as tyrosyl- DNA phosphodiesterase, nucleases and/or the coordinated action of nucleotide excision repair and homologous[grantome.com] Recruited to sites of UV damage and interacts with ubiquitinated PCNA and RAD18, the E3 ubiquitin ligase that monoubiquitinates PCNA.[ghr.nlm.nih.gov] Mol Genet Genomic Med 2018; 6(6):1148-1156 PMID: 30393977 Horvath S, Oshima J, Martin GM, Lu AT, Quach A, Cohen H, Felton S, Matsuyama M, Lowe D, Kabacik S, Wilson JG, Reiner[pathology.washington.edu]

  • Giardia Lamblia

    Abstract Epsins serve as recruitment platforms for clathrin membrane coat protein components and induce membrane curvature via their N-terminal homology (ENTH) domain.[ncbi.nlm.nih.gov] Ramesh for isolation and sequence of Giardia Rad18 , to Robert B. Moore for partial T. vaginalis Spo11 sequence, to Justine M.[doi.org] Smith, David S. Reiner and Frances D.[doi.org]