Luk Vandenberghe, PhD
Associate Professor of Ophthalmology, Massachusetts Eye and Ear Infirmary
A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear.
Authors: Authors: Landegger LD, Pan B, Askew C, Wassmer SJ, Gluck SD, Galvin A, Taylor R, Forge A, Stankovic KM, Holt JR, Vandenberghe LH.
Nat Biotechnol
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Nat Biotechnol
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Progress in gene therapy for neurological disorders.
Authors: Authors: Simonato M, Bennett J, Boulis NM, Castro MG, Fink DJ, Goins WF, Gray SJ, Lowenstein PR, Vandenberghe LH, Wilson TJ, Wolfe JH, Glorioso JC.
Nat Rev Neurol
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Nat Rev Neurol
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Efficient gene transfer into the mouse lung by fetal intratracheal injection of rAAV2/6.2.
Authors: Authors: Carlon M, Toelen J, Van der Perren A, Vandenberghe LH, Reumers V, Sbragia L, Gijsbers R, Baekelandt V, Himmelreich U, Wilson JM, Deprest J, Debyser Z.
Mol Ther
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Mol Ther
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Specific AAV serotypes stably transduce primary hippocampal and cortical cultures with high efficiency and low toxicity.
Authors: Authors: Royo NC, Vandenberghe LH, Ma JY, Hauspurg A, Yu L, Maronski M, Johnston J, Dichter MA, Wilson JM, Watson DJ.
Brain Res
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Brain Res
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Immunogenicity of an AAV-based, room-temperature stable, single dose COVID-19 vaccine in mice and non-human primates.
Authors: Authors: Zabaleta N, Dai W, Bhatt U, Chichester JA, Sanmiguel J, Estelien R, Michalson KT, Diop C, Maciorowski D, Qi W, Hudspeth E, Cucalon A, Dyer CD, Pampena MB, Knox JJ, LaRocque RC, Charles RC, Li D, Kim M, Sheridan A, Storm N, Johnson RI, Feldman J, Hauser BM, Zinn E, Ryan A, Kobayashi DT, Chauhan R, McGlynn M, Ryan ET, Schmidt AG, Price B, Honko A, Griffiths A, Yaghmour S, Hodge R, Betts MR, Freeman MW, Wilson JM, Vandenberghe LH.
bioRxiv
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bioRxiv
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Novel engineered, membrane-localized variants of vascular endothelial growth factor (VEGF) protect retinal ganglion cells: a proof-of-concept study.
Authors: Authors: Shen J, Xiao R, Bair J, Wang F, Vandenberghe LH, Dartt D, Baranov P, Ng YSE.
Cell Death Dis
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Cell Death Dis
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Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c.
Authors: Authors: Pan B, Askew C, Galvin A, Heman-Ackah S, Asai Y, Indzhykulian AA, Jodelka FM, Hastings ML, Lentz JJ, Vandenberghe LH, Holt JR, Géléoc GS.
Nat Biotechnol
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Nat Biotechnol
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Retinal gene therapy coming of age.
Naturally occurring singleton residues in AAV capsid impact vector performance and illustrate structural constraints.
Authors: Authors: Vandenberghe LH, Breous E, Nam HJ, Gao G, Xiao R, Sandhu A, Johnston J, Debyser Z, Agbandje-McKenna M, Wilson JM.
Gene Ther
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Gene Ther
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AAV as an immunogen.