REPAIRtoire - a database of DNA repair pathways
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First author
Title
PubMed ID
Wright J
A high frequency of distinct ATM gene mutations in ataxia-telangiectasia.
8808599
Philipova D
A hierarchy of SSB protomers in replication protein A.
8804316
Tyynismaa H
A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions.
19664747
Nick McElhinny SA
A gradient of template dependence defines distinct biological roles for family X polymerases in nonhomologous end joining.
16061182
Osterod M
A global DNA repair mechanism involving the Cockayne syndrome B (CSB) gene product can prevent the in vivo accumulation of endogenous oxidative DNA base damage.
12447686
Luca JW
A germline missense mutation R337C in exon 10 of the human p53 gene.
9452042
Law JC
A germ line mutation in exon 5 of the p53 gene in an extended cancer family.
1933902
Wilson TE
A genomics-based screen for yeast mutants with an altered recombination/end-joining repair ratio.
12399380
Medicherla B
A genomic screen identifies Dsk2p and Rad23p as essential components of ER-associated degradation.
15167887
McKee AE
A genome-wide in situ hybridization map of RNA-binding proteins reveals anatomically restricted expression in the developing mouse brain.
16033648
Adeyemo A
A genome-wide association study of hypertension and blood pressure in African Americans.
19609347
Collins JE
A genome annotation-driven approach to cloning the human ORFeome.
15461802
Wilmes GM
A genetic interaction map of RNA-processing factors reveals links between Sem1/Dss1-containing complexes and mRNA export and splicing.
19061648
Clementz T
A gene coding for 3-deoxy-D-manno-octulosonic-acid transferase in Escherichia coli. Identification, mapping, cloning, and sequencing.
2033061
Lee SJ
A functional role for the p62-ERK1 axis in the control of energy homeostasis and adipogenesis.
20154642
Miranda-Carboni GA
A functional link between Wnt signaling and SKP2-independent p27 turnover in mammary tumors.
19056892
Lin W
A full-length cDNA of hREV3 is predicted to encode DNA polymerase zeta for damage-induced mutagenesis in humans.
10102035
Li L
A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans.
12055248
Hernandez D
A family showing no evidence of linkage between the ataxia telangiectasia gene and chromosome 11q22-23.
8445618
Jin J
A family of diverse Cul4-Ddb1-interacting proteins includes Cdt2, which is required for S phase destruction of the replication factor Cdt1.
16949367
van Belzen MJ
A double missense mutation in the ATM gene of a Dutch family with ataxia telangiectasia.
9521587
Raynard S
A double Holliday junction dissolvasome comprising BLM, topoisomerase IIIalpha, and BLAP75.
16595695
Wilkinson DS
A direct intersection between p53 and transforming growth factor beta pathways targets chromatin modification and transcription repression of the alpha-fetoprotein gene.
15657445
Gastaldello S
A deneddylase encoded by Epstein-Barr virus promotes viral DNA replication by regulating the activity of cullin-RING ligases.
20190741
Lebel M
A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity.
9789047
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