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Anja Raams

Showing results (21-30 of 45) with videos related to

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Brain : a Journal of Neurology|June 24, 2008
Neurological symptoms and natural course of xeroderma pigmentosumAnu Anttinen, Leena Koulu, Eeva Nikoskelainen, et al.
Plos Genetics|May 3, 2013
Disruption of TTDA results in complete nucleotide excision repair deficiency and embryonic lethalityArjan F Theil, Julie Nonnekens, Barbara Steurer, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelinationLaila Shehata, Dimitre R Simeonov, Anja Raams, et al.
Plos One|May 1, 2015
Attenuated XPC expression is not associated with impaired DNA repair in bladder cancerKishan A T Naipal, Anja Raams, Serena T Bruens, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
Molecular analysis of mutations in DNA polymerase eta in xeroderma pigmentosum-variant patientsBernard C Broughton, Agnes Cordonnier, Wim J Kleijer, et al.
The Journal of Clinical Investigation|December 17, 2005
A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutationMirjam van der Burg, Lieneke R van Veelen, Nicole S Verkaik, et al.
Nature Genetics|June 29, 2004
A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group AGiuseppina Giglia-Mari, Frederic Coin, Jeffrey A Ranish, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
SMARCAL1 deficiency predisposes to non-Hodgkin lymphoma and hypersensitivity to genotoxic agents in vivoAlireza Baradaran-Heravi, Anja Raams, Joanna Lubieniecka, et al.
Human Molecular Genetics|June 16, 2009
Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorderRolf J R J Janssen, Felix Distelmaier, Roel Smeets, et al.
Molecular Cell|November 15, 2024
STK19 drives transcription-coupled repair by stimulating repair complex stability, RNA Pol II ubiquitylation, and TFIIH recruitmentAnisha R Ramadhin, Shun-Hsiao Lee, Di Zhou, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Brain : a Journal of Neurology|June 24, 2008
Neurological symptoms and natural course of xeroderma pigmentosumAnu Anttinen, Leena Koulu, Eeva Nikoskelainen, et al.
Plos Genetics|May 3, 2013
Disruption of TTDA results in complete nucleotide excision repair deficiency and embryonic lethalityArjan F Theil, Julie Nonnekens, Barbara Steurer, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelinationLaila Shehata, Dimitre R Simeonov, Anja Raams, et al.
Plos One|May 1, 2015
Attenuated XPC expression is not associated with impaired DNA repair in bladder cancerKishan A T Naipal, Anja Raams, Serena T Bruens, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
Molecular analysis of mutations in DNA polymerase eta in xeroderma pigmentosum-variant patientsBernard C Broughton, Agnes Cordonnier, Wim J Kleijer, et al.
The Journal of Clinical Investigation|December 17, 2005
A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutationMirjam van der Burg, Lieneke R van Veelen, Nicole S Verkaik, et al.
Nature Genetics|June 29, 2004
A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group AGiuseppina Giglia-Mari, Frederic Coin, Jeffrey A Ranish, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
SMARCAL1 deficiency predisposes to non-Hodgkin lymphoma and hypersensitivity to genotoxic agents in vivoAlireza Baradaran-Heravi, Anja Raams, Joanna Lubieniecka, et al.
Human Molecular Genetics|June 16, 2009
Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorderRolf J R J Janssen, Felix Distelmaier, Roel Smeets, et al.
Molecular Cell|November 15, 2024
STK19 drives transcription-coupled repair by stimulating repair complex stability, RNA Pol II ubiquitylation, and TFIIH recruitmentAnisha R Ramadhin, Shun-Hsiao Lee, Di Zhou, et al.
Pageof 5