D. Hoogstraten

发表

Action of DNA repair endonuclease ERCC1/XPF in living cells.

A. Houtsmuller, J. Hoeijmakers, W. Vermeulen, 1999, Science.

Rapid switching of TFIIH between RNA polymerase I and II transcription and DNA repair in vivo.

A. Houtsmuller, J. Hoeijmakers, R. van Driel, 2002, Molecular cell.

Xeroderma Pigmentosum Group A Protein Loads as a Separate Factor onto DNA Lesions

M. J. Moné, A. Houtsmuller, J. Hoeijmakers, 2003, Molecular and Cellular Biology.

Mathematical modeling of nucleotide excision repair reveals efficiency of sequential assembly strategies.

R. Heinrich, M. J. Moné, A. Houtsmuller, 2005, Molecular cell.

An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria.

C. D. De Zeeuw, J. Hoeijmakers, W. Vermeulen, 2006, Cancer cell.

Dynamic Interaction of TTDA with TFIIH Is Stabilized by Nucleotide Excision Repair in Living Cells

J. Hoeijmakers, G. Giglia-Mari, W. Vermeulen, 2006, PLoS biology.

TFIIH Plays an Essential Role in RNA Polymerase I Transcription

I. Grummt, D. Hoogstraten, J. Egly, 2002, Cell.

UV-DDB-dependent regulation of nucleotide excision repair kinetics in living cells.

A. Houtsmuller, J. Hoeijmakers, W. Vermeulen, 2009, DNA repair.

Versatile DNA damage detection by the global genome nucleotide excision repair protein XPC

A. Houtsmuller, J. Hoeijmakers, W. Vermeulen, 2008, Journal of Cell Science.

First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure.

J. Hoeijmakers, G. Giglia-Mari, W. Vermeulen, 2007, American journal of human genetics.

A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A

R. Aebersold, J. Ranish, J. Hoeijmakers, 2004, Nature Genetics.

DNA damage stabilizes interaction of CSB with the transcription elongation machinery

W. V. van Cappellen, A. Houtsmuller, J. Hoeijmakers, 2004, The Journal of cell biology.

DNA damage triggers nucleotide excision repair-dependent monoubiquitylation of histone H2A.

J. Neefjes, A. Houtsmuller, J. Hoeijmakers, 2006, Genes & development.

Rescue of Progeria in Trichothiodystrophy by Homozygous Lethal Xpd Alleles

J. Hoeijmakers, J. Jans, D. Hoogstraten, 2006, PLoS biology.

C-terminal UBA domains protect ubiquitin receptors by preventing initiation of protein degradation

D. Hoogstraten, N. Dantuma, K. Ács, 2011, Nature communications.

The spatio-temporal organization of DNA-repair: a live cell study

D. Hoogstraten, 2003 .

Isolation of Additional Bacteriophages with Genomes of Segmented Double-Stranded RNA

M. Romantschuk, J. Qiao, L. Mindich, 1999, Journal of bacteriology.

Condensed chromatin domains in the mammalian nucleus are accessible to large macromolecules

E. Manders, A. Houtsmuller, R. van Driel, 2003, EMBO reports.

monoubiquitylation of histone H 2 A DNA damage triggers nucleotide excision repair-dependent data

Wim, J. Neefjes, A. Houtsmuller, 2006 .

The ubiquitin receptor Rad23: at the crossroads of nucleotide excision repair and proteasomal degradation.

D. Hoogstraten, N. Dantuma, C. Heinen, 2009, DNA repair.