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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