Researcher
Nisha Nair
- Keywords:Medicine
Affiliations
- Basic (bio-) Medical Sciences (Department)
Member
From1 Oct 2017 → 30 Sep 2020 - Faculty of Medicine and Pharmacy (Faculty)
Member
From5 Aug 2015 → 31 May 2017 - Basic (bio-) Medical Sciences (Department)
Member
From1 Jan 2014 → 30 Sep 2020 - Division of Gene Therapy & Regenerative Medicine (Research group)
Member
From1 Dec 2011 → 1 Oct 2020 - Cell Biology and Histology (Department)
Member
From1 Dec 2011 → 31 Dec 2013
Projects
1 - 1 of 1
- "CURE-DMD": Development of Next-Generation Gene Therapy for Duchenne Muscular DystrophyFrom1 Oct 2017 → 30 Sep 2020Funding: FWO fellowships
Publications
1 - 10 of 11
- Gene Therapy For Hemophilia B Using CB 2679d-GT: A Novel Factor IX Variant With Higher Potency Than Factor IX Padua(2021)
Authors: Nisha Nair, Dries De Wolf, Phuong Anh Nguyen, Hong Quang Pham, Ermira Samara-Kuko, Jeff Landau, Grant E.Blouse, Marinee K Chuah, Thierry VandenDriessche
Pages: 2902-2906 - Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cells(2018)
Authors: Sumitava Dastidar, Simon Ardui, Kshitiz Singh, Debanjana Majumdar, Nisha Nair, Yanfang Fu, Deepak Reyon, Ermira Samara, Mattia FM Gerbil, Arnaud F. Klein, et al.
Pages: 8275-8298 - Efficient In Vivo Liver-Directed Gene Editing Using CRISPR/Cas9(2018)
Authors: Kshitiz Singh, Hanneke Evens, Nisha Nair, Melvin Rincon Acelas, Shilpita Sarcar, Ermira Samara, Marinee K Chuah, Thierry VandenDriessche
Pages: 1241-1254 - AAV9 delivered bispecific nanobody attenuates amyloid burden in the gelsolin amyloidosis mouse model(2017)
Authors: Adriaan Verhelle, Nisha Nair, Inge Everaert, Wouter Van Overbeke, Lynn Supply, Olivier Zwaenepoel, Cindy Peleman, Jo Van Dorpe, Tony Lahoutte, Nick Devoogdt, et al.
Pages: 1353-1364 - Next-Generation Gene Therapy for Hemophilia B using Hyperfunctional Coagulation Factor IX.(2017)
Authors: 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)
Authors: Nisha Nair
Pages: 2478 - 2492 - FANCA Knockout in Human Embryonic Stem Cells Causes a Severe Growth Disadvantage(2014)
Authors: Nisha Nair
Pages: 240-250 - Computationally designed liver-specific transcriptional cis-regulatory modules and hyper-functional factor IX improve liver-targeted gene therapy for hemophilia B.(2014)
Authors: Nisha Nair, M.y. Rincon, Hanneke Evens, Shilpita Sarcar, Ermira Samara, O. Ghandeharian, H. Viecelli, B. Thony, Pieter De Bleser
Pages: 3195-3199 - Liver-Specific Transcriptional Modules Identified by Genome-Wide in Silico Analysis Enable Efficient Gene Therapy in Mice and Non-Human Primates.(2014)
Authors: 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.
Pages: 1605-1613 - Gene therapy for hemophilia A and B(2013)
Authors: Nisha Nair
Pages: 391-402Number of pages: 12