about
New functions of Ctf18-RFC in preserving genome stability outside its role in sister chromatid cohesion.Genetic and biochemical analysis of Msh2p-Msh6p: role of ATP hydrolysis and Msh2p-Msh6p subunit interactions in mismatch base pair recognition.The 26S proteasome drives trinucleotide repeat expansionsRapid unwinding of triplet repeat hairpins by Srs2 helicase of Saccharomyces cerevisiaeMrc1, Tof1 and Csm3 inhibit CAG.CTG repeat instability by at least two mechanisms.The Saccharomyces cerevisiae Mre11-Rad50-Xrs2 complex promotes trinucleotide repeat expansions independently of homologous recombination.Inhibition of FEN-1 processing by DNA secondary structure at trinucleotide repeatsMismatch repair in replication fidelity, genetic recombination, and cancer biologyPartial reconstitution of DNA large loop repair with purified proteins from Saccharomyces cerevisiaeAnc1, a protein associated with multiple transcription complexes, is involved in postreplication repair pathway in S. cerevisiae.A selective inhibitor of histone deacetylase 3 prevents cognitive deficits and suppresses striatal CAG repeat expansions in Huntington's disease miceEfficient repair of large DNA loops in Saccharomyces cerevisiaeStabilizing effects of interruptions on trinucleotide repeat expansions in Saccharomyces cerevisiaeCis-elements governing trinucleotide repeat instability in Saccharomyces cerevisiae.CAG*CTG repeat instability in cultured human astrocytesPostreplication repair inhibits CAG.CTG repeat expansions in Saccharomyces cerevisiae.Histone deacetylase complexes as caretakers of genome stability.DNA elements important for CAG*CTG repeat thresholds in Saccharomyces cerevisiae.DNA polymerase delta, RFC and PCNA are required for repair synthesis of large looped heteroduplexes in Saccharomyces cerevisiae.Characterization of a DNA mismatch-binding activity in yeast extracts.Saccharomyces cerevisiae Srs2 DNA helicase selectively blocks expansions of trinucleotide repeats.Expansions of CAG.CTG repeats in immortalized human astrocytes.MutSβ abundance and Msh3 ATP hydrolysis activity are important drivers of CTG•CAG repeat expansions.Nucleotide excision repair and the 26S proteasome function together to promote trinucleotide repeat expansions.RTEL1 inhibits trinucleotide repeat expansions and fragility.RTEL1 Inhibits Trinucleotide Repeat Expansions and FragilityRev1 enhances CAG.CTG repeat stability in Saccharomyces cerevisiaeGenetic assays for triplet repeat instability in yeastCorrection of large mispaired DNA loops by extracts of Saccharomyces cerevisiaeDifferential effects of the mismatch repair genes MSH2 and MSH3 on homeologous recombination in Saccharomyces cerevisiaeCommunication between polypeptide chains in aspartate transcarbamoylase. Conformational changes at the active sites of unliganded chains resulting from ligand binding to other chainsThe influence of quaternary structure on the active site of an oligomeric enzyme. Catalytic subunit of aspartate transcarbamoylase
P50
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P50
description
Forscher
@de
chercheur
@fr
investigador
@es
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
研究者
@zh
name
Robert Lahue
@ast
Robert Lahue
@en
Robert Lahue
@es
Robert Lahue
@nl
type
label
Robert Lahue
@ast
Robert Lahue
@en
Robert Lahue
@es
Robert Lahue
@nl
altLabel
Robert S. Lahue
@en
prefLabel
Robert Lahue
@ast
Robert Lahue
@en
Robert Lahue
@es
Robert Lahue
@nl
P106
P31
P496
0000-0002-8870-5616