Related references
Note: Only part of the references are listed.The PCNA binding domain of Rad2p plays a role in mutagenesis by modulating the cell cycle in response to DNA damage
Sung-Lim Yu et al.
DNA REPAIR (2014)
Novel XPG (ERCC5) Mutations Affect DNA Repair and Cell Survival after Ultraviolet but not Oxidative Stress
Daniela T. Soltys et al.
HUMAN MUTATION (2013)
Characterization of Three XPG-Defective Patients Identifies Three Missense Mutations that Impair Repair and Transcription
Annika Schaefer et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2013)
Sequential and Multistep Substrate Interrogation Provides the Scaffold for Specificity in Human Flap Endonuclease 1
Mohamed A. Sobhy et al.
CELL REPORTS (2013)
Xeroderma pigmentosum complementation group G patient with a novel homozygous missense mutation and no neurological abnormalities
Shinichi Moriwaki et al.
EXPERIMENTAL DERMATOLOGY (2012)
Facilities for macromolecular crystallography at the Helmholtz-Zentrum Berlin
Uwe Mueller et al.
JOURNAL OF SYNCHROTRON RADIATION (2012)
Double strand binding-single strand incision mechanism for human flap endonuclease: Implications for the superfamily
Susan E. Tsutakawa et al.
MECHANISMS OF AGEING AND DEVELOPMENT (2012)
Structural and functional characterization of interactions involving the Tfb1 subunit of TFIIH and the NER factor Rad2
Julien Lafrance-Vanasse et al.
NUCLEIC ACIDS RESEARCH (2012)
Flap endonucleases pass 5′-flaps through a flexible arch using a disorder-thread-order mechanism to confer specificity for free 5′-ends
Nikesh Patel et al.
NUCLEIC ACIDS RESEARCH (2012)
Human Flap Endonuclease Structures, DNA Double-Base Flipping, and a Unified Understanding of the FEN1 Superfamily
Susan E. Tsutakawa et al.
CELL (2011)
Structures of Human Exonuclease 1 DNA Complexes Suggest a Unified Mechanism for Nuclease Family
Jillian Orans et al.
CELL (2011)
The xeroderma pigmentosum pathway: Decision tree analysis of DNA quality
Hanspeter Naegeli et al.
DNA REPAIR (2011)
MolProbity: all-atom structure validation for macromolecular crystallography
Vincent B. Chen et al.
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY (2010)
Features and development of Coot
P. Emsley et al.
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY (2010)
PHENIX: a comprehensive Python-based system for macromolecular structure solution
Paul D. Adams et al.
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY (2010)
Substrate recognition and catalysis by flap endonucleases and related enzymes
Christopher G. Tomlinson et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2010)
Mechanism of Holliday junction resolution by the human GEN1 protein
Ulrich Rass et al.
GENES & DEVELOPMENT (2010)
Coordination of dual incision and repair synthesis in human nucleotide excision repair
Lidija Staresincic et al.
EMBO JOURNAL (2009)
Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity
James E. Cleaver et al.
NATURE REVIEWS GENETICS (2009)
Identification of Holliday junction resolvases from humans and yeast
Stephen C. Y. Ip et al.
NATURE (2008)
Crystal structure of bacteriophage T4 5' nuclease in complex with a branched DNA reveals how flap endonuclease-1 family nucleases bind their substrates
Juliette M. Devos et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Phaser crystallographic software
Airlie J. McCoy et al.
JOURNAL OF APPLIED CRYSTALLOGRAPHY (2007)
Harnessing homologous recombination in vitro to generate recombinant DNA via SLIC
Mamie Z. Li et al.
NATURE METHODS (2007)
Making and breaking nucleic acids:: Two-Mg2+-ion catalysis and substrate specificity
W Yang et al.
MOLECULAR CELL (2006)
The spacer region of XPG mediates recruitment to nucleotide excision repair complexes and determines substrate specificity
I Dunand-Sauthier et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Structural basis for recruitment of human flap endonuclease 1 to PCNA
S Sakurai et al.
EMBO JOURNAL (2005)
Ordered conformational changes in damaged DNA induced by nucleotide excision repair factors
A Tapias et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damage
F Thorel et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
GeneSilico protein structure prediction meta-server
MA Kurowski et al.
NUCLEIC ACIDS RESEARCH (2003)
Structural determinants for substrate binding and catalysis by the structure-specific endonuclease XPG
M Hohl et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy
AR Lehmann
BIOCHIMIE (2003)
Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients
S Emmert et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2002)
The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity
P Lalle et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2002)
Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy
DI Zafeiriou et al.
PEDIATRIC RESEARCH (2001)
Share Paper
