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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 variants
Mark 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 modes
Frederik 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 pathway
Peter 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 future
Lene 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 repair
Joyce 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) photoproducts
Jun-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 changes
Meindert 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 combination
Cristina 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 significance
Lene 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 syndrome
Emily Rayner, Yvonne Tiersma, Cristina Fortuno, et al.
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of 8
Search research articles
Search
Showing results (31-40 of 78) with videos related to
Sort By:
Page
of 8
Human Mutation
|
November 22, 2011
A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants
Mark 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 modes
Frederik 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 pathway
Peter 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 future
Lene 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 repair
Joyce 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) photoproducts
Jun-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 changes
Meindert 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 combination
Cristina 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 significance
Lene 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 syndrome
Emily Rayner, Yvonne Tiersma, Cristina Fortuno, et al.
Page
of 8