Derick G Wansink

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 12

Top Topics

Systematic Review

Duchenne Muscular Dystrophy

Top Venues

Nature communications

International journal of molecular sciences

Stem cell reviews and reports

RNA (New York, N.Y.)

This page only lists publications with an associated author ORCID identifier.

Publications

Tayma Handal, Sarah Juster, Manar Abu Diab, Shira Yanovsky-Dagan, Fouad Zahdeh, Uria Aviel, Roni Sarel-Gallily, Shir Michael, Ester Bnaya, Shulamit Sebban, Yosef Buganim, Yotam Drier, Vincent Mouly, Stefan Kubicek, Walther J A A van den Broek, Derick G Wansink, Silvina Epsztejn-Litman, Rachel Eiges
Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locus. Nature communications 15 (1) (2024)
Tayma Handal, Sarah Juster, Manar Abu Diab, Shira Yanovsky-Dagan, Fouad Zahdeh, Uria Aviel, Roni Sarel-Gallily, Shir Michael, Ester Bnaya, Shulamit Sebban, Yosef Buganim, Yotam Drier, Vincent Mouly, Stefan Kubicek, Walther J A A van den Broek, Derick G Wansink, Silvina Epsztejn-Litman, Rachel Eiges
Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locus. Nature communications 15 (1) (2024)
Tayma Handal, Sarah Juster, Manar Abu Diab, Shira Yanovsky-Dagan, Fouad Zahdeh, Uria Aviel, Roni Sarel-Gallily, Shir Michael, Ester Bnaya, Shulamit Sebban, Yosef Buganim, Yotam Drier, Vincent Mouly, Stefan Kubicek, Walther J A A van den Broek, Derick G Wansink, Silvina Epsztejn-Litman, Rachel Eiges
Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locus. Nature communications 15 (1) (2024)
Renée H L Raaijmakers, C Rosanne M Ausems, Marieke Willemse, Sarah A Cumming, Baziel G M van Engelen, Darren G Monckton, Hans van Bokhoven, Derick G Wansink
Ameliorated cellular hallmarks of myotonic dystrophy in hybrid myotubes from patient and unaffected donor cells. Stem cell research & therapy 15 (1) (2024)
Tayma Handal, Sarah Juster, Manar Abu Diab, Shira Yanovsky-Dagan, Fouad Zahdeh, Uria Aviel, Roni Sarel-Gallily, Shir Michael, Ester Bnaya, Shulamit Sebban, Yosef Buganim, Yotam Drier, Vincent Mouly, Stefan Kubicek, Walther J A A van den Broek, Derick G Wansink, Silvina Epsztejn-Litman, Rachel Eiges
Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locus. Nature communications 15 (1) (2024)
Max J F Degener, Remco T P van Cruchten, Brittney A Otero, Eric T Wang, Derick G Wansink, Peter A C 't Hoen
A comprehensive atlas of fetal splicing patterns in the brain of adult myotonic dystrophy type 1 patients. NAR genomics and bioinformatics 4 (1) (2022)
C Rosanne M Ausems, Baziel G M van Engelen, Hans van Bokhoven, Derick G Wansink
Systemic cell therapy for muscular dystrophies : The ultimate transplantable muscle progenitor cell and current challenges for clinical efficacy. Stem cell reviews and reports 17 (3) (2020)
Remco T P van Cruchten, Bé Wieringa, Derick G Wansink
Expanded CUG repeats in DMPK transcripts adopt diverse hairpin conformations without influencing the structure of the flanking sequences. RNA (New York, N.Y.) 25 (4) (2019)
Renée H L Raaijmakers, Lise Ripken, C Rosanne M Ausems, Derick G Wansink
CRISPR/Cas Applications in Myotonic Dystrophy: Expanding Opportunities. International journal of molecular sciences 20 (15) (2019)
Laurène M André, Remco T P van Cruchten, Marieke Willemse, Derick G Wansink
(CTG)n repeat-mediated dysregulation of MBNL1 and MBNL2 expression during myogenesis in DM1 occurs already at the myoblast stage. PloS one 14 (5) (2019)
Laurène M André, Remco T P van Cruchten, Marieke Willemse, Karel Bezstarosti, Jeroen A A Demmers, Ellen L van Agtmaal, Derick G Wansink, Bé Wieringa
Recovery in the Myogenic Program of Congenital Myotonic Dystrophy Myoblasts after Excision of the Expanded (CTG)n Repeat. International journal of molecular sciences 20 (22) (2019)
M Leontien van der Bent, Omar Paulino da Silva Filho, Judith van Luijk, Roland Brock, Derick G Wansink
Assisted delivery of antisense therapeutics in animal models of heritable neurodegenerative and neuromuscular disorders: a systematic review and meta-analysis. Scientific reports 8 (1) (2018)