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First author	Title	PubMed ID
Lewinski ND	Detection of aldolase activity on polyacrylamide gels: application to 2-keto-4-hydroxyglutarate aldolase.	354428
DeLeo AB	Detection of a transformation-related antigen in chemically induced sarcomas and other transformed cells of the mouse.	221923
Sirois S	Detection of XerC and XerD recombinases in gram-negative bacteria of the family Enterobacteriaceae.	7608100
Kawano M	Detection of 5'- and 3'-UTR-derived small RNAs and cis-encoded antisense RNAs in Escherichia coli.	15718303
Kob R	Detection and identification of transcription factors as interaction partners of alien in vivo.	17438371
Kunarso G	Detailed characterization of the mouse embryonic stem cell transcriptome reveals novel genes and intergenic splicing associated with pluripotency.	18400104
Lee SB	Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni Syndrome.	11719428
Xia HC	Deregulated expression of the Per1 and Per2 in human gliomas.	20481271
Scheidtmann KH	Dephosphorylation of simian virus 40 large-T antigen and p53 protein by protein phosphatase 2A: inhibition by small-t antigen.	1848668
Johnson RE	Deoxynucleotide triphosphate binding mode conserved in Y family DNA polymerases.	12665597
Masuda Y	Deoxycytidyl transferase activity of the human REV1 protein is closely associated with the conserved polymerase domain.	11278384
Koivisto P	Demethylation of 3-methylthymine in DNA by bacterial and human DNA dioxygenases.	15269201
Ono R	Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality.	16341224
Cang Y	Deletion of DDB1 in mouse brain and lens leads to p53-dependent elimination of proliferating cells.	17129780
Boorstein RJ	Definitive identification of mammalian 5-hydroxymethyluracil DNA N-glycosylase activity as SMUG1.	11526119
Hsu HL	Defining interactions between DNA-PK and ligase IV/XRCC4.	12509254
Trapp C	Deficiency of the Cockayne syndrome B (CSB) gene aggravates the genomic instability caused by endogenous oxidative DNA base damage in mice.	17213818
Akhter S	Deficiency in SNM1 abolishes an early mitotic checkpoint induced by spindle stress.	15542852
Zhou T	Deficiency in 3'-phosphoglycolate processing in human cells with a hereditary mutation in tyrosyl-DNA phosphodiesterase (TDP1).	15647511
Rossi DJ	Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age.	17554309
Takayama K	Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy.	8571952
Takayama K	Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D.	7585650
Mann MB	Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome.	15703196
Mukhopadhyay SS	Defective mitochondrial peroxiredoxin-3 results in sensitivity to oxidative stress in Fanconi anemia.	17060495
Liu J	Defective interplay of activators and repressors with TFIH in xeroderma pigmentosum.	11239393

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