Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Marinee K, Chuah"'
Autor:
Sergio Muñoz, Joan Bertolin, Veronica Jimenez, Maria Luisa Jaén, Miquel Garcia, Anna Pujol, Laia Vilà, Victor Sacristan, Elena Barbon, Giuseppe Ronzitti, Jihad El Andari, Warut Tulalamba, Quang Hong Pham, Jesus Ruberte, Thierry VandenDriessche, Marinee K. Chuah, Dirk Grimm, Federico Mingozzi, Fatima Bosch
Publikováno v:
Molecular Metabolism, Vol 81, Iss , Pp 101899- (2024)
Objective: Pompe disease (PD) is caused by deficiency of the lysosomal enzyme acid α-glucosidase (GAA), leading to progressive glycogen accumulation and severe myopathy with progressive muscle weakness. In the Infantile-Onset PD (IOPD), death genera
Externí odkaz:
https://doaj.org/article/51f4889c5f3c445fbc764529166584d8
Autor:
Jonas Weinmann, Sabrina Weis, Josefine Sippel, Warut Tulalamba, Anca Remes, Jihad El Andari, Anne-Kathrin Herrmann, Quang H. Pham, Christopher Borowski, Susanne Hille, Tanja Schönberger, Norbert Frey, Martin Lenter, Thierry VandenDriessche, Oliver J. Müller, Marinee K. Chuah, Thorsten Lamla, Dirk Grimm
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-12 (2020)
Adeno-associated virus is the basis of many gene therapies and gene transfer vectors. Here the authors report a pipeline to enable side-by-side comparison of pre-selected capsids in a high throughput manner.
Externí odkaz:
https://doaj.org/article/fcda7a44d2044540880d0f383706efd9
Publikováno v:
Molecular therapy : the journal of the American Society of Gene Therapy. 30(12)
Autor:
Jaitip Tipanee, Ermira Samara-Kuko, Thierry Gevaert, Marinee K. Chuah, Thierry VandenDriessche
Allogeneic CD19-specific chimeric antigen receptor (CAR) T cells with inactivated donor T cell receptor (TCR) expression can be used as an "off-the-shelf" therapeutic modality for lymphoid malignancies, thus offering an attractive alternative to auto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac7c20b01c9712273deacef0e8b6d162
https://hdl.handle.net/20.500.14017/b85a3a4c-051f-455c-9710-29d2e688ae6d
https://hdl.handle.net/20.500.14017/b85a3a4c-051f-455c-9710-29d2e688ae6d
AAV9 delivered bispecific nanobody attenuates amyloid burden in the gelsolin amyloidosis mouse model
Autor:
Adriaan Verhelle, Lynn Supply, Thierry Vandendriessche, Olivier Zwaenepoel, Marinee K Chuah, Cindy Peleman, Jan Gettemans, Tony Lahoutte, Nisha Nair, Nick Devoogdt, Wim Derave, Inge Everaert, Wouter Van Overbeke, Jo Van Dorpe
Publikováno v:
ResearcherID
Gelsolin amyloidosis is a dominantly inherited, incurable type of amyloidosis. A single point mutation in the gelsolin gene (G654A is most common) results in the loss of a Ca2+ binding site in the second gelsolin domain. Consequently, this domain par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dec09a43eab319b7c3e4e92b447c4c5
https://hdl.handle.net/20.500.14017/864eadef-40ed-4e81-aefe-4f9bebb9cd4a
https://hdl.handle.net/20.500.14017/864eadef-40ed-4e81-aefe-4f9bebb9cd4a
Autor:
Marinee K, Chuah
Publikováno v:
Current gene therapy. 15(4)
Autor:
Marinee K Chuah
Publikováno v:
Current Gene Therapy. 15:327-328
Autor:
Kshitiz Singh, Hanneke Evens, Melvin Rincón, Nisha Nair, Shilpita Sarcar, Ermira Samara-Kuko, Marinee K. Chuah, Thierry VandenDriessche
Publikováno v:
Molecular Therapy. 24:S50
Autor:
Frédéric Pâques, Linda Popplewell, Olivier Danos, Philippe Duchateau, Diane Le Clerre, Roman Galetto, Sophie Leduc, Frédéric Lemaire, George Dickson, Céline Lebuhotel, Marinee K. Chuah, Christophe Perez, Danusia Oficjalska, Valérie Guyot, Laurent Poirot, Mariana Loperfido, Thierry VandenDriessche, Frédéric Cédrone, Julianne Smith, Fabien Delacôte, Taeyoung Koo, Fayza Daboussi, Kahina Oussedik, Sylvestre Grizot, Isabelle Chion-Sotinel, Mikhail Zaslavskiy, Aymeric Duclert, Rafael J. Yáñez-Muñoz, Agnès Gouble, Jean-Charles Epinat, Aurélie Dupuy
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2012, 40 (13), pp.6367-6379. ⟨10.1093/nar/gks268⟩
Nucleic Acids Research, Oxford University Press, 2012, 40 (13), pp.6367-6379. ⟨10.1093/nar/gks268⟩
The ability to specifically engineer the genome of living cells at precise locations using rare-cutting designer endonucleases has broad implications for biotechnology and medicine, particularly for functional genomics, transgenics and gene therapy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::606f73b816695da060d9688c750c4865
https://repository.royalholloway.ac.uk/items/058505dc-7d01-2380-fdd3-7ceaabbcb4f2/6/
https://repository.royalholloway.ac.uk/items/058505dc-7d01-2380-fdd3-7ceaabbcb4f2/6/
Autor:
Liesbeth De Waele, Chantal Thys, Marinee K Chuah, Kathleen Freson, Desire Collen, Christel Van Geet, Thierry Vandendriessche
The prevalence of congenital platelet disorders has not been established but for some life-threatening bleeding disorders the current therapies are not adequate, justifying the development of alternative strategies as gene therapy. In the case of pla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53ef518bddd49633cd6a4774ded2d956
https://biblio.vub.ac.be/vubir/development-of-megakaryocytespecific-lentiviral-vectors-for-gene-therapy-of-platelet-disorders(d321369f-7a9f-4fe8-8632-de64c5efacc3).html
https://biblio.vub.ac.be/vubir/development-of-megakaryocytespecific-lentiviral-vectors-for-gene-therapy-of-platelet-disorders(d321369f-7a9f-4fe8-8632-de64c5efacc3).html