Found: 17
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Two E3 ubiquitin ligases, SCF-Skp2 and DDB1-Cul4, target human Cdt1 for proteolysis.
- Published in:
- EMBO Journal, 2006, v. 25, n. 5, p. 1126, doi. 10.1038/sj.emboj.7601002
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- Article
Xeroderma pigmentosum group F protein binds to Eg5 and is required for proper mitosis: implications for XP-F and XFE.
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- Genes to Cells, 2012, v. 17, n. 3, p. 173, doi. 10.1111/j.1365-2443.2012.01582.x
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- Article
Constructive rescue of TFIIH instability by an alternative isoform of XPD derived from a mutated XPD allele in mild but not severe XP-D/CS.
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- Journal of Human Genetics, 2015, v. 60, n. 5, p. 259, doi. 10.1038/jhg.2015.18
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- Article
A Japanese trichothiodystrophy patient with XPD mutations.
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- Journal of Human Genetics, 2011, v. 56, n. 1, p. 77, doi. 10.1038/jhg.2010.123
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- Article
Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair.
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- Nature Genetics, 2012, v. 44, n. 5, p. 593, doi. 10.1038/ng.2228
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- Article
RPAP3 interacts with Reptin to regulate UV-induced phosphorylation of H2AX and DNA damage.
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- Journal of Cellular Biochemistry, 2009, v. 106, n. 5, p. 920, doi. 10.1002/jcb.22073
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- Article
Mutant Cockayne syndrome group B protein inhibits repair of DNA topoisomerase I-DNA covalent complex.
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- Genes to Cells, 2011, v. 16, n. 1, p. 101, doi. 10.1111/j.1365-2443.2010.01467.x
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- Article
A novel cytoplasmic GTPase XAB1 interacts with DNA repair protein XPA.
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- Nucleic Acids Research, 2000, v. 28, n. 21, p. 4212, doi. 10.1093/nar/28.21.4212
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- Article
Mutational analysis of a function of xeroderma pigmentosum group A (XPA) protein instrand‐specific DNA repair.
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- Nucleic Acids Research, 1998, v. 26, n. 20, p. 4662, doi. 10.1093/nar/26.20.4662
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- Article
Sequential Binding of DNA Repair Proteins RPA and ERCC1 to XPA in vitro.
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- Nucleic Acids Research, 1996, v. 24, n. 23, p. 4719, doi. 10.1093/nar/24.23.4719
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- Article
Inhibition of UVSSA ubiquitination suppresses transcription‐coupled nucleotide excision repair deficiency caused by dissociation from USP7.
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- FEBS Journal, 2018, v. 285, n. 5, p. 965, doi. 10.1111/febs.14382
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- Article
Xeroderma pigmentosum A homolog from Hydra partially complements DNA repair defect in human XPA-deficient cells.
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- Journal of Biosciences, 2021, v. 46, n. 2, p. 1, doi. 10.1007/s12038-021-00170-6
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- Article
Solution structure of the DNA- and RPA-binding domain of the human repair factor XPA.
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- Nature Structural Biology, 1998, v. 5, n. 8, p. 701, doi. 10.1038/1400
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- Article
Structural basis of ubiquitin recognition by the winged-helix domain of Cockayne syndrome group B protein.
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- Nucleic Acids Research, 2019, v. 47, n. 7, p. 3784, doi. 10.1093/nar/gkz081
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- Article
BRCA1 contributes to transcription-coupled repair of DNA damage through polyubiquitination and degradation of Cockayne syndrome B protein.
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- Cancer Science, 2011, v. 102, n. 10, p. 1840, doi. 10.1111/j.1349-7006.2011.02037.x
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- Article
Mutations in the XPD gene leading to xeroderma pigmentosum symptoms.
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- Human Mutation, 1997, v. 9, n. 4, p. 322, doi. 10.1002/(SICI)1098-1004(1997)9:4<322::AID-HUMU4>3.0.CO;2-7
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- Article
Resonance Assignments, Solution Structure, and Backbone Dynamics of the DNA- and RPA-Binding Domain of Human Repair Factor XPA1.
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- Journal of Biochemistry, 1999, v. 125, n. 3, p. 495, doi. 10.1093/oxfordjournals.jbchem.a022313
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- Article