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Niels de Wind

Showing results (31-40 of 78) with videos related to

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Human Mutation|November 22, 2011
A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variantsMark Drost, José B M Zonneveld, Sandrine van Hees, et al.
DNA Repair|July 15, 2011
The Rev1 translesion synthesis polymerase has multiple distinct DNA binding modesFrederik H de Groote, Jacob G Jansen, Yuji Masuda, et al.
European Journal of Immunology|July 17, 2013
Rev1 is essential in generating G to C transversions downstream of the Ung2 pathway but not the Msh2+Ung2 hybrid pathwayPeter Hugo Lodewijk Krijger, Anastasia Tsaalbi-Shtylik, Niek Wit, et al.
Human Mutation|July 27, 2012
Pathological assessment of mismatch repair gene variants in Lynch syndrome: past, present, and futureLene Juel Rasmussen, Christopher D Heinen, Brigitte Royer-Pokora, et al.
The EMBO Journal|January 13, 2006
Dual role of MutS glutamate 38 in DNA mismatch discrimination and in the authorization of repairJoyce H G Lebbink, Dubravka Georgijevic, Ganesh Natrajan, et al.
DNA Repair|January 9, 2020
Effect of sequence context on Polζ-dependent error-prone extension past (6-4) photoproductsJun-Ichi Akagi, Keiji Hashimoto, Kenji Suzuki, et al.
The Journal of Biological Chemistry|August 7, 2004
ATP increases the affinity between MutS ATPase domains. Implications for ATP hydrolysis and conformational changesMeindert H Lamers, Dubravka Georgijevic, Joyce H Lebbink, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 28, 2009
Abrogation of microsatellite-instable tumors using a highly selective suicide gene/prodrug combinationCristina Ferrás, Joachim A F Oude Vrielink, Johan W A Verspuy, et al.
Human Mutation|April 5, 2013
Response to: Design of a core classification process for DNA mismatch repair variations of a priori unknown functional significanceLene Juel Rasmussen, Christopher D Heinen, Brigitte Royer-Pokora, et al.
Human Mutation|April 22, 2022
Predictive functional assay-based classification of PMS2 variants in Lynch syndromeEmily Rayner, Yvonne Tiersma, Cristina Fortuno, et al.
Pageof 8

Showing results (31-40 of 78) with videos related to

Sort By:
Pageof 8
Human Mutation|November 22, 2011
A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variantsMark Drost, José B M Zonneveld, Sandrine van Hees, et al.
DNA Repair|July 15, 2011
The Rev1 translesion synthesis polymerase has multiple distinct DNA binding modesFrederik H de Groote, Jacob G Jansen, Yuji Masuda, et al.
European Journal of Immunology|July 17, 2013
Rev1 is essential in generating G to C transversions downstream of the Ung2 pathway but not the Msh2+Ung2 hybrid pathwayPeter Hugo Lodewijk Krijger, Anastasia Tsaalbi-Shtylik, Niek Wit, et al.
Human Mutation|July 27, 2012
Pathological assessment of mismatch repair gene variants in Lynch syndrome: past, present, and futureLene Juel Rasmussen, Christopher D Heinen, Brigitte Royer-Pokora, et al.
The EMBO Journal|January 13, 2006
Dual role of MutS glutamate 38 in DNA mismatch discrimination and in the authorization of repairJoyce H G Lebbink, Dubravka Georgijevic, Ganesh Natrajan, et al.
DNA Repair|January 9, 2020
Effect of sequence context on Polζ-dependent error-prone extension past (6-4) photoproductsJun-Ichi Akagi, Keiji Hashimoto, Kenji Suzuki, et al.
The Journal of Biological Chemistry|August 7, 2004
ATP increases the affinity between MutS ATPase domains. Implications for ATP hydrolysis and conformational changesMeindert H Lamers, Dubravka Georgijevic, Joyce H Lebbink, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 28, 2009
Abrogation of microsatellite-instable tumors using a highly selective suicide gene/prodrug combinationCristina Ferrás, Joachim A F Oude Vrielink, Johan W A Verspuy, et al.
Human Mutation|April 5, 2013
Response to: Design of a core classification process for DNA mismatch repair variations of a priori unknown functional significanceLene Juel Rasmussen, Christopher D Heinen, Brigitte Royer-Pokora, et al.
Human Mutation|April 22, 2022
Predictive functional assay-based classification of PMS2 variants in Lynch syndromeEmily Rayner, Yvonne Tiersma, Cristina Fortuno, et al.
Pageof 8