Onderzoeker
Nisha Nair
- Trefwoorden:Geneeskunde
Affiliaties
- Basis (bio)-medische wetenschappen (Departement)
Lid
Vanaf1 okt 2017 → 30 sep 2020 - Faculteit van de Geneeskunde en Farmacie (Faculteit)
Lid
Vanaf5 aug 2015 → 31 mei 2017 - Basis (bio)-medische wetenschappen (Departement)
Lid
Vanaf1 jan 2014 → 30 sep 2020 - Gentherapie & Regeneratieve Geneeskunde (Onderzoeksgroep)
Lid
Vanaf1 dec 2011 → 1 okt 2020 - Celbiologie en Histologie (Departement)
Lid
Vanaf1 dec 2011 → 31 dec 2013
Projecten
1 - 1 of 1
- “CURE-DMD”: Ontwikkeling van verbeterde gentherapie strategieën voor de ziekte van DuchenneVanaf1 okt 2017 → 30 sep 2020Financiering: FWO mandaten
Publicaties
1 - 10 van 11
- Gene Therapy For Hemophilia B Using CB 2679d-GT: A Novel Factor IX Variant With Higher Potency Than Factor IX Padua(2021)
Auteurs: Nisha Nair, Dries De Wolf, Phuong Anh Nguyen, Hong Quang Pham, Ermira Samara-Kuko, Jeff Landau, Grant E.Blouse, Marinee K Chuah, Thierry VandenDriessche
Pagina's: 2902-2906 - Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cells(2018)
Auteurs: Sumitava Dastidar, Simon Ardui, Kshitiz Singh, Debanjana Majumdar, Nisha Nair, Yanfang Fu, Deepak Reyon, Ermira Samara, Mattia FM Gerbil, Arnaud F. Klein, et al.
Pagina's: 8275-8298 - Efficient In Vivo Liver-Directed Gene Editing Using CRISPR/Cas9(2018)
Auteurs: Kshitiz Singh, Hanneke Evens, Nisha Nair, Melvin Rincon Acelas, Shilpita Sarcar, Ermira Samara, Marinee K Chuah, Thierry VandenDriessche
Pagina's: 1241-1254 - AAV9 delivered bispecific nanobody attenuates amyloid burden in the gelsolin amyloidosis mouse model(2017)
Auteurs: Adriaan Verhelle, Nisha Nair, Inge Everaert, Wouter Van Overbeke, Lynn Supply, Olivier Zwaenepoel, Cindy Peleman, Jo Van Dorpe, Tony Lahoutte, Nick Devoogdt, et al.
Pagina's: 1353-1364 - Next-Generation Gene Therapy for Hemophilia B using Hyperfunctional Coagulation Factor IX.(2017)
Auteurs: Nisha Nair, Marinee K Chuah
- Baboon envelope pseudotyped lentiviral vectors efficiently
transduce human B cells and allow active factor IX B cell secretion in vivo in NOD/SCIDcc-/- mice(2016)
Auteurs: Nisha Nair
Pagina's: 2478 - 2492 - FANCA Knockout in Human Embryonic Stem Cells Causes a Severe Growth Disadvantage(2014)
Auteurs: Nisha Nair
Pagina's: 240-250 - Computationally designed liver-specific transcriptional cis-regulatory modules and hyper-functional factor IX improve liver-targeted gene therapy for hemophilia B.(2014)
Auteurs: Nisha Nair, M.y. Rincon, Hanneke Evens, Shilpita Sarcar, Ermira Samara, O. Ghandeharian, H. Viecelli, B. Thony, Pieter De Bleser
Pagina's: 3195-3199 - Liver-Specific Transcriptional Modules Identified by Genome-Wide in Silico Analysis Enable Efficient Gene Therapy in Mice and Non-Human Primates.(2014)
Auteurs: I. Petrus, P De Bleser, Caroline Le Guiner, G. Gernoux, O. Adjali, Nisha Nair, Jessica Willems, Hanneke Evens, M.y. Rincon, Janka Matrai, et al.
Pagina's: 1605-1613 - Gene therapy for hemophilia A and B(2013)
Auteurs: Nisha Nair
Pagina's: 391-402Aantal pagina's: 12