עקוב אחר
adrian thrasher
adrian thrasher
UCL/GOSH
כתובת אימייל מאומתת בדומיין ucl.ac.uk
כותרת
צוטט על ידי
צוטט על ידי
שנה
Effect of gene therapy on visual function in Leber's congenital amaurosis
JWB Bainbridge, AJ Smith, SS Barker, S Robbie, R Henderson, ...
New England Journal of Medicine 358 (21), 2231-2239, 2008
23922008
Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy
S Hacein-Bey-Abina, F Le Deist, F Carlier, C Bouneaud, C Hue, ...
New england journal of medicine 346 (16), 1185-1193, 2002
14502002
Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients
SJ Howe, MR Mansour, K Schwarzwaelder, C Bartholomae, M Hubank, ...
The Journal of clinical investigation 118 (9), 2008
14352008
Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1
MG Ott, M Schmidt, K Schwarzwaelder, S Stein, U Siler, U Koehl, H Glimm, ...
Nature medicine 12 (4), 401-409, 2006
13732006
Molecular remission of infant B-ALL after infusion of universal TALEN gene-edited CAR T cells
W Qasim, H Zhan, S Samarasinghe, S Adams, P Amrolia, S Stafford, ...
Science translational medicine 9 (374), eaaj2013, 2017
9512017
Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease
S Stein, MG Ott, S Schultze-Strasser, A Jauch, B Burwinkel, A Kinner, ...
Nature medicine 16 (2), 198-204, 2010
9052010
Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector
HB Gaspar, KL Parsley, S Howe, D King, KC Gilmour, J Sinclair, G Brouns, ...
The Lancet 364 (9452), 2181-2187, 2004
8302004
A robust model for read count data in exome sequencing experiments and implications for copy number variant calling
V Plagnol, J Curtis, M Epstein, KY Mok, E Stebbings, S Grigoriadou, ...
Bioinformatics 28 (21), 2747-2754, 2012
6842012
The cytoplasm of living cells behaves as a poroelastic material
E Moeendarbary, L Valon, M Fritzsche, AR Harris, DA Moulding, ...
Nature materials 12 (3), 253-261, 2013
6702013
High-level transduction and gene expression in hematopoietic repopulating cells using a human imunodeficiency virus type 1-based lentiviral vector containing an internal spleen …
C Demaison, K Parsley, G Brouns, M Scherr, K Battmer, C Kinnon, M Grez, ...
Human gene therapy 13 (7), 803-813, 2002
6222002
Effective gene therapy with nonintegrating lentiviral vectors
RJ Yánez-Munoz, KS Balaggan, A MacNeil, SJ Howe, M Schmidt, ...
Nature medicine 12 (3), 348-353, 2006
5702006
Hematopoietic stem-cell gene therapy for cerebral adrenoleukodystrophy
F Eichler, C Duncan, PL Musolino, PJ Orchard, S De Oliveira, AJ Thrasher, ...
New England Journal of Medicine 377 (17), 1630-1638, 2017
5142017
The wiskott-aldrich syndrome
HD Ochs, AJ Thrasher
Journal of Allergy and Clinical Immunology 117 (4), 725-738, 2006
5082006
Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency
C Picard, H Von Bernuth, P Ghandil, M Chrabieh, O Levy, PD Arkwright, ...
Medicine 89 (6), 403-425, 2010
4822010
The European Society for Immunodeficiencies (ESID) registry working definitions for the clinical diagnosis of inborn errors of immunity
MG Seidel, G Kindle, B Gathmann, I Quinti, M Buckland, J van Montfrans, ...
The Journal of Allergy and Clinical Immunology: In Practice 7 (6), 1763-1770, 2019
4602019
A modified γ-retrovirus vector for X-linked severe combined immunodeficiency
S Hacein-Bey-Abina, SY Pai, HB Gaspar, M Armant, CC Berry, S Blanche, ...
New England Journal of Medicine 371 (15), 1407-1417, 2014
4602014
Insertional transformation of hematopoietic cells by self-inactivating lentiviral and gammaretroviral vectors
U Modlich, S Navarro, D Zychlinski, T Maetzig, S Knoess, MH Brugman, ...
Molecular Therapy 17 (11), 1919-1928, 2009
4592009
WASP: a key immunological multitasker
AJ Thrasher, SO Burns
Nature Reviews Immunology 10 (3), 182-192, 2010
4442010
Outcomes following gene therapy in patients with severe Wiskott-Aldrich syndrome
SHB Abina, HB Gaspar, J Blondeau, L Caccavelli, S Charrier, K Buckland, ...
Jama 313 (15), 1550-1563, 2015
4252015
Comprehensive rare variant analysis via whole-genome sequencing to determine the molecular pathology of inherited retinal disease
KJ Carss, G Arno, M Erwood, J Stephens, A Sanchis-Juan, S Hull, K Megy, ...
The American Journal of Human Genetics 100 (1), 75-90, 2017
4082017
המערכת אינה יכולה לבצע את הפעולה כעת. נסה שוב מאוחר יותר.
מאמרים 1–20