Helicase-inactivating mutations as a basis for dominant negative phenotypes

Sequence-specific processing of telomeric 3' overhangs by the Werner syndrome protein exonuclease activity

(2016) Baomin Li et al.   Aging-US

WRN helicase defective in the premature aging disorder Werner syndrome genetically interacts with topoisomerase 3 and restores the top3 slow growth phenotype of sgs1 top3

(2016) Monika Aggarwal et al.   Aging-US

Cooperation of DNA-PKcs and WRN helicase in the maintenance of telomeric D-loops

(2016) Rika Kusumoto-Matsuo et al.   Aging-US

Unique and important consequences of RECQ1 deficiency in mammalian cells

(2011) Sudha Sharma et al.   CELL CYCLE

WRN helicase promotes repair of DNA double-strand breaks caused by aberrant mismatch repair of chromium-DNA adducts

(2010) Alma Zecevic et al.   CELL CYCLE

Whither the replisome: Emerging perspectives on the dynamic nature of the DNA replication machinery

(2010) Lance D. Langston et al.   CELL CYCLE

Genetic mutants illuminate the roles of RecQ helicases in recombinational repair or response to replicational stress

(2010) Monika Aggarwal et al.   CELL CYCLE

RecQ4: the second replicative helicase?

(2010) Christopher Capp et al.   CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY

Delineation of WRN helicase function with EXO1 in the replicational stress response

(2010) Monika Aggarwal et al.   DNA REPAIR

FANCJ: Solving problems in DNA replication

(2010) Kevin Hiom   DNA REPAIR

Helicase and translocases required for the maintenance of genome stability

(2010) Simon J. Boulton   DNA REPAIR

Distinct roles of RECQ1 in the maintenance of genomic stability

(2010) Yuliang Wu et al.   DNA REPAIR

Human RECQL5 overcomes thymidine-induced replication stress

(2010) Rachel Blundred et al.   DNA REPAIR

Roles of Werner syndrome protein in protection of genome integrity

(2010) Marie L. Rossi et al.   DNA REPAIR

Rothmund–Thomson syndrome helicase, RECQ4: On the crossroad between DNA replication and repair

(2010) Yilun Liu   DNA REPAIR

Mammalian Fbh1 is important to restore normal mitotic progression following decatenation stress

(2010) Corentin Laulier et al.   DNA REPAIR

Unwinding the functions of the Pif1 family helicases

(2010) Matthew L. Bochman et al.   DNA REPAIR

Yeast as a model system to study RecQ helicase function

(2010) Thomas M. Ashton et al.   DNA REPAIR

RECQL5 helicase: Connections to DNA recombination and RNA polymerase II transcription

(2010) Ozan Aygün et al.   DNA REPAIR

Mitochondrial helicases and mitochondrial genome maintenance

(2010) Nadja C. de Souza-Pinto et al.   MECHANISMS OF AGEING AND DEVELOPMENT

BACH1/FANCJ Acts with TopBP1 and Participates Early in DNA Replication Checkpoint Control

(2010) Zihua Gong et al.   MOLECULAR CELL

Targeting the FANCJ–BRCA1 interaction promotes a switch from recombination to polη-dependent bypass

(2010) J Xie et al.   ONCOGENE

The Caenorhabditis elegans Werner Syndrome Protein Functions Upstream of ATR and ATM in Response to DNA Replication Inhibition and Double-Strand DNA Breaks

(2010) Se-Jin Lee et al.   PLoS Genetics

How the Fanconi Anemia Pathway Guards the Genome

(2009) George-Lucian Moldovan et al.   Annual Review of Genetics

FANCJ Helicase Operates in the Fanconi Anemia DNA Repair Pathway and the Response to Replicational Stress

(2009) Yuliang Wu et al.   CURRENT MOLECULAR MEDICINE

FANCJ Uses Its Motor ATPase to Destabilize Protein-DNA Complexes, Unwind Triplexes, and Inhibit RAD51 Strand Exchange

(2009) Joshua A. Sommers et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Human Fbh1 helicase contributes to genome maintenance via pro- and anti-recombinase activities

(2009) Kasper Fugger et al.   JOURNAL OF CELL BIOLOGY

Human Dna2 Is a Nuclear and Mitochondrial DNA Maintenance Protein

(2009) J. P. Duxin et al.   MOLECULAR AND CELLULAR BIOLOGY

Fanconi anemia and its diagnosis

(2009) Arleen D. Auerbach   MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS

Welcome the Family of FANCJ-like Helicases to the Block of Genome Stability Maintenance Proteins

(2008) Y. Wu et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome

(2008) T. R. Singh et al.   GENES & DEVELOPMENT

RMI, a new OB-fold complex essential for Bloom syndrome protein to maintain genome stability

(2008) D. Xu et al.   GENES & DEVELOPMENT

Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling

(2008) Steffi Goffart et al.   HUMAN MOLECULAR GENETICS

UvrD and UvrD252 Counteract RecQ, RecJ, and RecFOR in a rep Mutant of Escherichia coli

(2008) R. Lestini et al.   JOURNAL OF BACTERIOLOGY

FANCJ Is a Structure-specific DNA Helicase Associated with the Maintenance of Genomic G/C Tracts

(2008) Timothy B. C. London et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

FANCJ Helicase Defective in Fanconia Anemia and Breast Cancer Unwinds G-Quadruplex DNA To Defend Genomic Stability

(2008) Y. Wu et al.   MOLECULAR AND CELLULAR BIOLOGY

Human DNA2 Is a Mitochondrial Nuclease/Helicase for Efficient Processing of DNA Replication and Repair Intermediates

(2008) Li Zheng et al.   MOLECULAR CELL

Non-hexameric DNA helicases and translocases: mechanisms and regulation

(2008) Timothy M. Lohman et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY