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Search Results - Ensinck, Marjolein M
Search Results - Ensinck, Marjolein M
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One Size Does Not Fit All: The Past, Present and Future of Cystic Fibrosis Causal Therapies
by
Ensinck, Marjolein M.
,
Carlon, Marianne S.
Published in
Cells (Basel, Switzerland)
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Novel CFTR modulator combinations maximise rescue of G85E and N1303K in rectal organoids
by
Ensinck, Marjolein M
,
De Keersmaecker, Liesbeth
,
Ramalho, Anabela S
,
Cuyx, Senne
,
Van Biervliet, Stephanie
,
Dupont, Lieven
,
Christ, Frauke
,
Debyser, Zeger
,
Vermeulen, François
,
Carlon, Marianne S
Published in
ERJ open research
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Functional restoration of a CFTR splicing mutation through RNA delivery of CRISPR adenine base editor
by
Amistadi, Simone
,
Maule, Giulia
,
Ciciani, Matteo
,
Ensinck, Marjolein M.
,
De Keersmaecker, Liesbeth
,
Ramalho, Anabela S.
,
Guidone, Daniela
,
Buccirossi, Martina
,
Galietta, Luis J.V.
,
Carlon, Marianne S.
,
Cereseto, Anna
Published in
Molecular therapy
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Nanoblades allow high-level genome editing in murine and human organoids
by
Tiroille, Victor
,
Krug, Adrien
,
Bokobza, Emma
,
Kahi, Michel
,
Bulcaen, Mattijs
,
Ensinck, Marjolein M.
,
Geurts, Maarten H.
,
Hendriks, Delilah
,
Vermeulen, François
,
Larbret, Frédéric
,
Gutierrez-Guerrero, Alejandra
,
Chen, Yu
,
Van Zundert, Indra
,
Rocha, Susana
,
Rios, Anne C.
,
Medaer, Louise
,
Gijsbers, Rik
,
Mangeot, Philippe E.
,
Clevers, Hans
,
Carlon, Marianne S.
,
Bost, Frédéric
,
Verhoeyen, Els
Published in
Molecular therapy. Nucleic acids
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Prime editing functionally corrects cystic fibrosis-causing CFTR mutations in human organoids and airway epithelial cells
by
Bulcaen, Mattijs
,
Kortleven, Phéline
,
Liu, Ronald B.
,
Maule, Giulia
,
Dreano, Elise
,
Kelly, Mairead
,
Ensinck, Marjolein M.
,
Thierie, Sam
,
Smits, Maxime
,
Ciciani, Matteo
,
Hatton, Aurelie
,
Chevalier, Benoit
,
Ramalho, Anabela S.
,
Casadevall i Solvas, Xavier
,
Debyser, Zeger
,
Vermeulen, François
,
Gijsbers, Rik
,
Sermet-Gaudelus, Isabelle
,
Cereseto, Anna
,
Carlon, Marianne S.
Published in
Cell reports. Medicine
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Severity of the S1251N allele in cystic fibrosis is affected by the presence of the F508C variant in cis
by
Cuyx, Senne
,
Ramalho, Sofia S.
,
Callebaut, Isabelle
,
Cuppens, Harry
,
Kmit, Arthur
,
Arnauts, Kaline
,
Ferrante, Marc
,
Verfaillie, Catherine
,
Ensinck, Marjolein
,
Carlon, Marianne S.
,
Boon, Mieke
,
Proesmans, Marijke
,
Dupont, Lieven
,
De Boeck, Kris
,
Farinha, Carlos M.
,
Vermeulen, François
,
Ramalho, Anabela S.
Published in
Journal of cystic fibrosis
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