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Anja Raams

Showing results (31-40 of 45) with videos related to

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International Journal of Hyperthermia : the Official Journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group|July 15, 2017
Heat-induced BRCA2 degradation in human tumours provides rationale for hyperthermia-PARP-inhibitor combination therapiesNathalie van den Tempel, Hanny Odijk, Netteke van Holthe, et al.
Nature|December 22, 2006
A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axisLaura J Niedernhofer, George A Garinis, Anja Raams, et al.
Molecular Cell|March 10, 2022
Active DNA damage eviction by HLTF stimulates nucleotide excision repairMarvin van Toorn, Yasemin Turkyilmaz, Sueji Han, et al.
Cancer Cell|August 15, 2006
An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeriaJaan-Olle Andressoo, James R Mitchell, Jan de Wit, et al.
Human Molecular Genetics|October 4, 2017
Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissueArjan F Theil, Imke K Mandemaker, Emile van den Akker, et al.
EMBO Molecular Medicine|October 6, 2023
Trichothiodystrophy-associated MPLKIP maintains DBR1 levels for proper lariat debranching and ectodermal differentiationArjan F Theil, Alex Pines, Tuğba Kalayci, et al.
American Journal of Human Genetics|April 30, 2013
Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemiaMassimo Bogliolo, Beatrice Schuster, Chantal Stoepker, et al.
Human Molecular Genetics|April 28, 2021
Protein instability associated with AARS1 and MARS1 mutations causes trichothiodystrophyElena Botta, Arjan F Theil, Anja Raams, et al.
American Journal of Human Genetics|August 3, 2019
Bi-allelic TARS Mutations Are Associated with Brittle Hair PhenotypeArjan F Theil, Elena Botta, Anja Raams, et al.
American Journal of Human Genetics|January 13, 2005
Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophyKazuhiko Nakabayashi, Daniela Amann, Yan Ren, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
International Journal of Hyperthermia : the Official Journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group|July 15, 2017
Heat-induced BRCA2 degradation in human tumours provides rationale for hyperthermia-PARP-inhibitor combination therapiesNathalie van den Tempel, Hanny Odijk, Netteke van Holthe, et al.
Nature|December 22, 2006
A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axisLaura J Niedernhofer, George A Garinis, Anja Raams, et al.
Molecular Cell|March 10, 2022
Active DNA damage eviction by HLTF stimulates nucleotide excision repairMarvin van Toorn, Yasemin Turkyilmaz, Sueji Han, et al.
Cancer Cell|August 15, 2006
An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeriaJaan-Olle Andressoo, James R Mitchell, Jan de Wit, et al.
Human Molecular Genetics|October 4, 2017
Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissueArjan F Theil, Imke K Mandemaker, Emile van den Akker, et al.
EMBO Molecular Medicine|October 6, 2023
Trichothiodystrophy-associated MPLKIP maintains DBR1 levels for proper lariat debranching and ectodermal differentiationArjan F Theil, Alex Pines, Tuğba Kalayci, et al.
American Journal of Human Genetics|April 30, 2013
Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemiaMassimo Bogliolo, Beatrice Schuster, Chantal Stoepker, et al.
Human Molecular Genetics|April 28, 2021
Protein instability associated with AARS1 and MARS1 mutations causes trichothiodystrophyElena Botta, Arjan F Theil, Anja Raams, et al.
American Journal of Human Genetics|August 3, 2019
Bi-allelic TARS Mutations Are Associated with Brittle Hair PhenotypeArjan F Theil, Elena Botta, Anja Raams, et al.
American Journal of Human Genetics|January 13, 2005
Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophyKazuhiko Nakabayashi, Daniela Amann, Yan Ren, et al.
Pageof 5