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Anja Raams

Showing results (11-20 of 45) with videos related to

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BMC Medical Genetics|January 13, 2018
Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPFIsabell Popp, Maqsood Punekar, Nick Telford, et al.
Journal of Cell Science|August 7, 2008
Versatile DNA damage detection by the global genome nucleotide excision repair protein XPCDeborah Hoogstraten, Steven Bergink, Jessica M Y Ng, et al.
EMBO Reports|August 15, 2018
DNA damage-induced replication stress results in PA200-proteasome-mediated degradation of acetylated histonesImke K Mandemaker, Marit E Geijer, Iris Kik, et al.
American Journal of Human Genetics|February 3, 2007
First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failureNicolaas G J Jaspers, Anja Raams, Margherita Cirillo Silengo, et al.
Nature Genetics|April 3, 2012
UV-sensitive syndrome protein UVSSA recruits USP7 to regulate transcription-coupled repairPetra Schwertman, Anna Lagarou, Dick H W Dekkers, et al.
Meta Gene|January 22, 2015
Pollitt syndrome patients carry mutation in TTDN1Sigrid M A Swagemakers, Nicolaas G J Jaspers, Anja Raams, et al.
Nucleic Acids Research|July 20, 2023
Different SWI/SNF complexes coordinately promote R-loop- and RAD52-dependent transcription-coupled homologous recombinationCarlota Davó-Martínez, Angela Helfricht, Cristina Ribeiro-Silva, et al.
Plos Genetics|March 12, 2010
Mislocalization of XPF-ERCC1 nuclease contributes to reduced DNA repair in XP-F patientsAnwaar Ahmad, Jacqueline H Enzlin, Nikhil R Bhagwat, et al.
Human Mutation|September 2, 2006
Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndromeKyu-Seon Oh, Sikandar G Khan, N G J Jaspers, et al.
The Journal of Cell Biology|June 30, 2026
Recruitment and release of XPG during NER is controlled by pre- and post-incision factors and EXO1Alba Muniesa-Vargas, Cristina Ribeiro-Silva, Carlota Davó-Martínez, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
BMC Medical Genetics|January 13, 2018
Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPFIsabell Popp, Maqsood Punekar, Nick Telford, et al.
Journal of Cell Science|August 7, 2008
Versatile DNA damage detection by the global genome nucleotide excision repair protein XPCDeborah Hoogstraten, Steven Bergink, Jessica M Y Ng, et al.
EMBO Reports|August 15, 2018
DNA damage-induced replication stress results in PA200-proteasome-mediated degradation of acetylated histonesImke K Mandemaker, Marit E Geijer, Iris Kik, et al.
American Journal of Human Genetics|February 3, 2007
First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failureNicolaas G J Jaspers, Anja Raams, Margherita Cirillo Silengo, et al.
Nature Genetics|April 3, 2012
UV-sensitive syndrome protein UVSSA recruits USP7 to regulate transcription-coupled repairPetra Schwertman, Anna Lagarou, Dick H W Dekkers, et al.
Meta Gene|January 22, 2015
Pollitt syndrome patients carry mutation in TTDN1Sigrid M A Swagemakers, Nicolaas G J Jaspers, Anja Raams, et al.
Nucleic Acids Research|July 20, 2023
Different SWI/SNF complexes coordinately promote R-loop- and RAD52-dependent transcription-coupled homologous recombinationCarlota Davó-Martínez, Angela Helfricht, Cristina Ribeiro-Silva, et al.
Plos Genetics|March 12, 2010
Mislocalization of XPF-ERCC1 nuclease contributes to reduced DNA repair in XP-F patientsAnwaar Ahmad, Jacqueline H Enzlin, Nikhil R Bhagwat, et al.
Human Mutation|September 2, 2006
Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndromeKyu-Seon Oh, Sikandar G Khan, N G J Jaspers, et al.
The Journal of Cell Biology|June 30, 2026
Recruitment and release of XPG during NER is controlled by pre- and post-incision factors and EXO1Alba Muniesa-Vargas, Cristina Ribeiro-Silva, Carlota Davó-Martínez, et al.
Pageof 5