Identification and Biochemical Characterization of a Novel Mutation inDDX11Causing Warsaw Breakage Syndrome

UBQLN2 mutations are rare in French and French–Canadian amyotrophic lateral sclerosis

(2012) Hussein Daoud et al.   NEUROBIOLOGY OF AGING

Regulation of translocation polarity by helicase domain 1 in SF2B helicases

(2011) Robert A Pugh et al.   EMBO JOURNAL

Functional and structural studies of the nucleotide excision repair helicase XPD suggest a polarity for DNA translocation

(2011) Jochen Kuper et al.   EMBO JOURNAL

Biochemical Characterization of Warsaw Breakage Syndrome Helicase

(2011) Yuliang Wu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1

(2010) Petra van der Lelij et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Fanconi anemia group J mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes

(2010) Y. Wu et al.   BLOOD

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