REPAIRtoire - a database of DNA repair pathways

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First author	Title	PubMed ID
Gonzalez-Vioque E	Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population.	16401742
Wu Y	Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations.	10521294
Smith NL	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	20445134
Yoshida T	Association of genetic variants with hemorrhagic stroke in Japanese individuals.	20198315
Yoshida T	Association of gene polymorphisms with chronic kidney disease in Japanese individuals.	19724895
Hirsch B	Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood.	14670928
Ye L	Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population.	9021029
Zhong Q	Association of BRCA1 with the hRad50-hMre11-p95 complex and the DNA damage response.	10426999
Orimo H	Association between single nucleotide polymorphisms in the hMSH3 gene and sporadic colon cancer with microsatellite instability.	10944853
Cohen D	Assignment of the human dUTPase gene (DUT) to chromosome 15q15-q21. 1 by fluorescence in situ hybridization.	9070952
Okumura K	Assignment of the 36.5-kDa (RFC5), 37-kDa (RFC4), 38-kDa (RFC3), and 40-kDa (RFC2) subunit genes of human replication factor C to chromosome bands 12q24.2-q24.3, 3q27, 13q12.3-q13, and 7q11.23.	7774928
Genuardi M	Assessment of pathogenicity criteria for constitutional missense mutations of the hereditary nonpolyposis colorectal cancer genes MLH1 and MSH2.	10573010
Oguri M	Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals.	19851296
Allen GC Jr	Assembly of the primosome of DNA replication in Escherichia coli.	8366072
Gasior SL	Assembly of RecA-like recombinases: distinct roles for mediator proteins in mitosis and meiosis.	11459983
Rothwell DG	Asparagine 212 is essential for abasic site recognition by the human DNA repair endonuclease HAP1.	8932375
Moshous D	Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.	11336668
Zhang X	Artemis is a phosphorylation target of ATM and ATR and is involved in the G2/M DNA damage checkpoint response.	15456891
Wang J	Artemis deficiency confers a DNA double-strand break repair defect and Artemis phosphorylation status is altered by DNA damage and cell cycle progression.	15811628
Qiu J	Arginine residues 47 and 70 of human flap endonuclease-1 are involved in DNA substrate interactions and cleavage site determination.	11986308
El-Andaloussi N	Arginine methylation regulates DNA polymerase beta.	16600869
Morales-Ruiz T	Arabidopsis thaliana Ogg1 protein excises 8-hydroxyguanine and 2,6-diamino-4-hydroxy-5-formamidopyrimidine from oxidatively damaged DNA containing multiple lesions.	12627976
Wall MK	Arabidopsis thaliana DNA gyrase is targeted to chloroplasts and mitochondria.	15136745
Wen R	Arabidopsis UEV1D promotes Lysine-63-linked polyubiquitination and is involved in DNA damage response.	18178771
Bagherieh-Najjar MB	Arabidopsis RecQsim, a plant-specific member of the RecQ helicase family, can suppress the MMS hypersensitivity of the yeast sgs1 mutant.	12856935

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