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Marleen Dekker

Showing results (11-20 of 24) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|March 7, 2009
Gene modification in embryonic stem cells by single-stranded DNA oligonucleotidesMarieke Aarts, Marleen Dekker, Rob Dekker, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 9, 2016
Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variantsHellen Houlleberghs, Marleen Dekker, Hildo Lantermans, et al.
Journal of Medical Genetics|December 1, 2019
Three-step site-directed mutagenesis screen identifies pathogenic <i>MLH1</i> variants associated with Lynch syndromeHellen Houlleberghs, Marleen Dekker, Jarnick Lusseveld, et al.
International Journal for Equity in Health|August 30, 2019
Leaving no one behind? Social inclusion of health insurance in low- and middle-income countries: a systematic reviewSuzanne G M van Hees, Timothy O'Fallon, Miranda Hofker, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 9, 2016
LNA modification of single-stranded DNA oligonucleotides allows subtle gene modification in mismatch-repair-proficient cellsThomas W van Ravesteyn, Marleen Dekker, Alexander Fish, et al.
Mutation Research|August 2, 2011
Transient suppression of MLH1 allows effective single-nucleotide substitution by single-stranded DNA oligonucleotidesMarleen Dekker, Sandra de Vries, Marieke Aarts, et al.
Elife|October 17, 2018
Loss of p53 suppresses replication-stress-induced DNA breakage in G1/S checkpoint deficient cellsBente Benedict, Tanja van Harn, Marleen Dekker, et al.
Gastroenterology|August 5, 2014
Temozolomide increases the number of mismatch repair-deficient intestinal crypts and accelerates tumorigenesis in a mouse model of Lynch syndromeKamila Wojciechowicz, Erika Cantelli, Bastiaan Van Gerwen, et al.
Plos Genetics|May 23, 2017
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicityHellen Houlleberghs, Anne Goverde, Jarnick Lusseveld, et al.
Cancer Research|July 25, 2014
RB family tumor suppressor activity may not relate to active silencing of E2F target genesTinke L Vormer, Kamila Wojciechowicz, Marleen Dekker, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Methods in Molecular Biology (Clifton, N.J.)|March 7, 2009
Gene modification in embryonic stem cells by single-stranded DNA oligonucleotidesMarieke Aarts, Marleen Dekker, Rob Dekker, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 9, 2016
Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variantsHellen Houlleberghs, Marleen Dekker, Hildo Lantermans, et al.
Journal of Medical Genetics|December 1, 2019
Three-step site-directed mutagenesis screen identifies pathogenic <i>MLH1</i> variants associated with Lynch syndromeHellen Houlleberghs, Marleen Dekker, Jarnick Lusseveld, et al.
International Journal for Equity in Health|August 30, 2019
Leaving no one behind? Social inclusion of health insurance in low- and middle-income countries: a systematic reviewSuzanne G M van Hees, Timothy O'Fallon, Miranda Hofker, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 9, 2016
LNA modification of single-stranded DNA oligonucleotides allows subtle gene modification in mismatch-repair-proficient cellsThomas W van Ravesteyn, Marleen Dekker, Alexander Fish, et al.
Mutation Research|August 2, 2011
Transient suppression of MLH1 allows effective single-nucleotide substitution by single-stranded DNA oligonucleotidesMarleen Dekker, Sandra de Vries, Marieke Aarts, et al.
Elife|October 17, 2018
Loss of p53 suppresses replication-stress-induced DNA breakage in G1/S checkpoint deficient cellsBente Benedict, Tanja van Harn, Marleen Dekker, et al.
Gastroenterology|August 5, 2014
Temozolomide increases the number of mismatch repair-deficient intestinal crypts and accelerates tumorigenesis in a mouse model of Lynch syndromeKamila Wojciechowicz, Erika Cantelli, Bastiaan Van Gerwen, et al.
Plos Genetics|May 23, 2017
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicityHellen Houlleberghs, Anne Goverde, Jarnick Lusseveld, et al.
Cancer Research|July 25, 2014
RB family tumor suppressor activity may not relate to active silencing of E2F target genesTinke L Vormer, Kamila Wojciechowicz, Marleen Dekker, et al.
Pageof 3