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Reynald Lescarbeau
Reynald Lescarbeau
Intellia Therapeutics
Verified email at intelliatx.com
Title
Cited by
Cited by
Year
A single administration of CRISPR/Cas9 lipid nanoparticles achieves robust and persistent in vivo genome editing
JD Finn, AR Smith, MC Patel, L Shaw, MR Youniss, J van Heteren, ...
Cell reports 22 (9), 2227-2235, 2018
6642018
Blood-based identification of non-responders to anti-TNF therapy in rheumatoid arthritis
TM Thomson, RM Lescarbeau, DA Drubin, D Laifenfeld, D de Graaf, ...
BMC medical genomics 8, 1-12, 2015
392015
In vitro model of metastasis to bone marrow mediates prostate cancer castration resistant growth through paracrine and extracellular matrix factors
RM Lescarbeau, FP Seib, M Prewitz, C Werner, DL Kaplan
Public Library of Science 7 (8), e40372, 2012
322012
Response to “Unexpected mutations after CRISPR–Cas9 editing in vivo
RM Lescarbeau, B Murray, TM Barnes, N Bermingham
Nature methods 15 (4), 237-237, 2018
252018
A single administration of CRISPR/Cas9 lipid nanoparticles achieves robust and persistent
JD Finn, AR Smith, MC Patel, L Shaw, MR Youniss, J Van Heteren, ...
in vivo genome editing. Cell Rep 22, 2227-2235, 2018
152018
A single administration of CRISPR/Cas9 lipid nanoparticles achieves robust and persistent in vivo genome editing, Cell Rep. 22 (2018) 2227–2235
JD Finn, AR Smith, MC Patel, L Shaw, MR Youniss, J van Heteren, ...
13
Quantitative analysis of castration resistant prostate cancer progression through phosphoproteome signaling
RM Lescarbeau, DL Kaplan
BMC cancer 14, 1-12, 2014
122014
Compositions and methods for the treatment of hemoglobinopathies
AE Boitano, M Cooke, LB Klickstein, R Lescarbeau, CS Mickanin, ...
112022
Compositions and methods for immunooncology
MW Chen, D Melissa, G Dranoff, CS Mackanin, R Lescarbeau, ...
US Patent App. 15/780,751, 2018
92018
CRISPR/Cas9 gene-edited hematopoietic stem cell therapy for sickle cell disease
WC Vionnie, Y Liu, M Curran, P Zhang, J Snead, C Schmedt, Y Yang, ...
Blood 130, 535, 2017
82017
A single administration of CRISPR/Cas9 lipid nanoparticles achieves robust and persistent in vivo genome editing. Cell Rep 2018; 22: 2227-35
JD Finn, AR Smith, MC Patel, L Shaw, MR Youniss, J van Heteren, ...
6
A single administration of CRISPR/Cas9 lipid nanoparticles achieves robust and persistent in vivo genome editing. Cell Rep 22 (9): 2227–2235
JD Finn, AR Smith, MC Patel, L Shaw, MR Youniss, J van Heteren, ...
52018
Development of NTLA-2001, a CRISPR/Cas9 genome editing therapeutic for the treatment of ATTR.
K Wood, M Pink, J Seitzer, N Gardner, S Alexander, T DiMezzo, A Amaral, ...
Liver 17 (19), 24, 2019
32019
A Novel Strategy for Off-the-Shelf T Cell Therapy Which Evades Allogeneic T Cell and NK Cell Rejection
Y Zhang, S Goel, A Prodeus, U Jetley, Y Tan, J Averill, U Ranade, ...
Blood 138, 1711, 2021
22021
Validation of CRISPR/Cas9 off-target discovery profiles from in silico prediction, cell-based and biochemical-based assays with targeted off-target sequencing
N Patel, B Han, B Murray, J Growe, P Salerno, R Lescarbeau, J Seitzer, ...
Mol Ther 28, 99, 2020
22020
Rescue of Amyloid Deposition Phenotype after Single-Treatment CRISPR/Cas9 Gene Editing in a Humanized Mouse Model of TTR Amyloidosis
MJ Saraiva, S Costelha, P Goncalves, A Teixeira, H Martins, T Dirstine, ...
MOLECULAR THERAPY 26 (5), 130-130, 2018
22018
A reanalysis of Schaefer et al. does not indicate extensive CRISPR/Cas9 mediated off-target editing events
RM Lescarbeau, B Murray, TM Barnes, N Bermingham
bioRxiv, 159608, 2017
22017
Compositions and methods for treating alpha-1 antitrypsin deficiency
S Odate, W Strapps, RM Lescarbeau
US Patent 11,549,107, 2023
12023
Compositions and Methods for Hydroxyacid Oxidase 1 (HAO1) Gene Editing for Treating Primary Hyperoxaluria Type 1 (PH1)
ZW Dymek, S Odate, BA Murray, RM Lescarbeau, A Huebner, W Strapps, ...
US Patent App. 17/162,377, 2021
12021
Compositions and Methods for TTR Gene Editing and Treating ATTR Amyloidosis
AMP Kanjolia, S Odate, JL Seitzer, RM Lescarbeau, W Strapps
US Patent App. 16/828,573, 2020
12020
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