Directed Evolution of AAV for Retinal Gene Therapy

被引：0

作者：

Tekinsoy, Muge D. ^{[1
]}

Planul, Arthur ^{[1
]}

Zin, Emilia ^{[1
]}

Simon, Cardillia J. ^{[1
]}

Desrosiers, Melissa ^{[1
]}

Fradot, Valerie ^{[1
]}

Nemoto, Takahiro ^{[1
]}

Robert, Camille ^{[1
]}

Jaillard, Celine ^{[1
]}

Bertin, Stephane ^{[1
,2
]}

Sahel, Jose-Alain ^{[1
,2
]}

Ferrari, Ulisse ^{[1
]}

Dalkara, Deniz ^{[1
]}

机构：

[1] Sorbonne Univ, INSERM, CNRS, Inst Vis, Paris, France

[2] CHNO Quinze Vingts, INSERM DGOS CIC 1423, Paris, France

来源：

MOLECULAR THERAPY | 2022年 / 30卷 / 04期

关键词：

D O I：

暂无

中图分类号：

Q81 [生物工程学（生物技术）]; Q93 [微生物学];

学科分类号：

071005 ; 0836 ; 090102 ; 100705 ;

摘要：

121

引用

页码：65 / 65

页数：1

共 50 条

[21] Delivering efficient liver-directed AAV-mediated gene therapy
J Baruteau
S N Waddington
I E Alexander
P Gissen
Gene Therapy, 2017, 24 : 263 - 264
[22] Tissue-Directed Transgene Engineering for AAV and Lentivector Gene Therapy Approaches
Brown, Harrison C.
Zakas, Phillip M.
George, Stephan N.
Parker, Ernest T.
Spencer, H. Trent
Doering, Christopher B.
MOLECULAR THERAPY, 2016, 24 : S287 - S287
[23] Delivering efficient liver-directed AAV-mediated gene therapy
Baruteau, J.
Waddington, S. N.
Alexander, I. E.
Gissen, P.
GENE THERAPY, 2017, 24 (05) : 263 - 264
[24] AAV Mediated Liver Directed Gene Therapy for Gyrate Atrophy of the Choroid and Retina
Boffa, Iolanda
Marrocco, Elena
Caterino, Marianna
Ruoppolo, Margherita
Auricchio, Alberto
Pierri, Nicola Brunetti
MOLECULAR THERAPY, 2022, 30 (04) : 247 - 247
[25] AAV-Directed Liver Gene Therapy for Crigler-Najjar Syndrome
Collaud, Fanny
Ronzitti, Giuseppe
Bortolussi, Giulia
Guianvarc'h, Laurence
Veron, Philippe
Charles, Severine
Vidal, Patrice
Sola, Marcelo Simon
Leborgne, Christian
Rundwasser, Stephanie
Dejoint, Ludivine
Goncalves, Delphine
Van Wittenberghe, Laetitia
Martin, Samia
Le Bec, Christine
Bosma, Piter J.
Muro, Andres F.
Hebben, Matthias
Mingozzi, Federico
MOLECULAR THERAPY, 2018, 26 (05) : 385 - 385
[26] Selection of Optimal AAV Serotypes as Clinical Candidates for AAV-Mediated, Liver-Directed Gene Therapy
Wang, Lili
Wang, Huan
Bell, Peter
McCarter, Robert J.
Calcedo, Roberto
Wilson, James M.
MOLECULAR THERAPY, 2009, 17 : S279 - S279
[27] AAV-Mediated Gene Therapy in Mouse Models of Recessive Retinal Degeneration
Pang, J. -J.
Lei, L.
Dai, X.
Shi, W.
Liu, X.
Dinculescu, A.
McDowell, J. H.
CURRENT MOLECULAR MEDICINE, 2012, 12 (03) : 316 - 330
[28] AAV-mediated gene therapy for retinal disorders: from mouse to man
P K Buch
J W Bainbridge
R R Ali
Gene Therapy, 2008, 15 : 849 - 857
[29] AAV-Mediated Gene Therapy for Retinal Disorders in Large Animal Models
Stieger, Knut
Lheriteau, Elsa
Moullier, Philippe
Rolling, Fabienne
ILAR JOURNAL, 2009, 50 (02) : 206 - 224
[30] AAV-mediated gene therapy for retinal disorders: from mouse to man
Buch, P. K.
Bainbridge, J. W.
Ali, R. R.
GENE THERAPY, 2008, 15 (11) : 849 - 857

← 1 2 3 4 5 →