Publications by authors named "Claudia Kerzendorfer"

18Publications

FANCD2 Promotes Meiotic Crossover Formation.

Plant Cell 2018 02 19;30(2):415-428. Epub 2018 Jan 19.

Department of Chromosome Biology, Max F. Perutz Laboratories, University of Vienna, Vienna Biocenter, 1030 Vienna, Austria

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http://dx.doi.org/10.1105/tpc.17.00745DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868695PMC
February 2018

A thesaurus of genetic variation for interrogation of repetitive genomic regions.

Nucleic Acids Res 2015 May 27;43(10):e68. Epub 2015 Mar 27.

Research Center for Molecular Medicine of the Austrian Academy of Sciences (CeMM), Vienna, Austria

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http://dx.doi.org/10.1093/nar/gkv178DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446415PMC
May 2015

Meier-Gorlin syndrome and Wolf-Hirschhorn syndrome: two developmental disorders highlighting the importance of efficient DNA replication for normal development and neurogenesis.

DNA Repair (Amst) 2013 Aug 23;12(8):637-44. Epub 2013 May 23.

Human DNA Damage Response Disorders Group, Genome Damage & Stability Centre, University of Sussex, Brighton, East Sussex BN1 9RQ, United Kingdom.

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http://dx.doi.org/10.1016/j.dnarep.2013.04.016DOI Listing
August 2013

Characterizing the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf-Hirschhorn syndrome.

Hum Mol Genet 2012 May 10;21(10):2181-93. Epub 2012 Feb 10.

Human DNA Damage Response Disorders Group, Genome Damage and Stability Centre, University of Sussex, Brighton BN1 9RQ, UK.

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http://dx.doi.org/10.1093/hmg/dds033DOI Listing
May 2012

Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.

Nat Genet 2011 Feb 27;43(4):350-5. Epub 2011 Feb 27.

Medical Research Council (MRC) Human Genetics Unit (HGU), Institute for Genetics and Molecular Medicine, Western General Hospital, Edinburgh, UK.

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http://dx.doi.org/10.1038/ng.776DOI Listing
February 2011

CUL4B-deficiency in humans: understanding the clinical consequences of impaired Cullin 4-RING E3 ubiquitin ligase function.

Mech Ageing Dev 2011 Aug 23;132(8-9):366-73. Epub 2011 Feb 23.

Human DNA Damage Response Disorders Group, Genome Damage and Stability Centre, University of Sussex, Brighton BN1 9RQ, UK.

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https://linkinghub.elsevier.com/retrieve/pii/S00476374110002
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http://dx.doi.org/10.1016/j.mad.2011.02.003DOI Listing
August 2011

UVB and caffeine: inhibiting the DNA damage response to protect against the adverse effects of UVB.

J Invest Dermatol 2009 Jul;129(7):1611-3

Human DNA Damage Response Disorders Group, Genome Damage & Stability Centre, University of Sussex, East Sussex, UK.

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http://dx.doi.org/10.1038/jid.2009.99DOI Listing
July 2009

Human DNA damage response and repair deficiency syndromes: linking genomic instability and cell cycle checkpoint proficiency.

DNA Repair (Amst) 2009 Sep 26;8(9):1139-52. Epub 2009 May 26.

Human DNA Damage Response Disorders Group, Genome Damage & Stability Centre, University of Sussex, Falmer, Brighton, East Sussex, BN1 9RQ, UK.

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http://dx.doi.org/10.1016/j.dnarep.2009.04.018DOI Listing
September 2009

Expression of the ubiquitin variant ubR48 decreases proteolytic activity in Arabidopsis and induces cell death.

Planta 2006 Mar 1;223(4):684-97. Epub 2005 Oct 1.

Institute of Botany, University of Vienna, Austria.

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http://dx.doi.org/10.1007/s00425-005-0121-zDOI Listing
March 2006