Thursday, March 3, 2016

Gene Therapy - Table of Contents alert Volume 23 Issue 3

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Gene Therapy

TABLE OF CONTENTS

Volume 23, Issue 3 (March 2016)

In this issue
Original Articles
Short Communication
Corrigendum

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Original Articles

Top

Co-expression of fibulin-5 and VEGF165 increases long-term patency of synthetic vascular grafts seeded with autologous endothelial cells

M Preis, J Schneiderman, B Koren, Y Ben-Yosef, D Levin-Ashkenazi, S Shapiro, T Cohen, M Blich, M Israeli-Amit, Y Sarnatzki, D Gershtein, R Shofti, B S Lewis, Y Shaul and M Y Flugelman

Gene Ther 2016 23: 237-246; advance online publication, December 24, 2015; 10.1038/gt.2015.104

Abstract | Full Text

rAAV-mediated overexpression of sox9, TGF-β and IGF-I in minipig bone marrow aspirates to enhance the chondrogenic processes for cartilage repair

J Frisch, A Rey-Rico, J K Venkatesan, G Schmitt, H Madry and M Cucchiarini

Gene Ther 2016 23: 247-255; advance online publication, November 19, 2015; 10.1038/gt.2015.106

Abstract | Full Text

A novel intranuclear RNA vector system for long-term stem cell modification

Y Ikeda, A Makino, W E Matchett, S J Holditch, B Lu, A B Dietz and K Tomonaga

Gene Ther 2016 23: 256-262; advance online publication, December 3, 2015; 10.1038/gt.2015.108

Abstract | Full Text

Mucopolysaccharidosis IIIB confers enhanced neonatal intracranial transduction by AAV8 but not by 5, 9 or rh10 OPEN

J A Gilkes, M D Bloom and C D Heldermon

Gene Ther 2016 23: 263-271; advance online publication, December 16, 2015; 10.1038/gt.2015.111

Abstract | Full Text

Healthy and diseased corticospinal motor neurons are selectively transduced upon direct AAV2-2 injection into the motor cortex OPEN

J H Jara, M J Stanford, Y Zhu, M Tu, W W Hauswirth, M C Bohn, S H DeVries and P H Özdinler

Gene Ther 2016 23: 272-282; advance online publication, January 21, 2016; 10.1038/gt.2015.112

Abstract | Full Text

AAV1/2-mediated BDNF gene therapy in a transgenic rat model of Huntington’s disease

B Connor, Y Sun, D von Hieber, S K Tang, K S Jones and C Maucksch

Gene Ther 2016 23: 283-295; advance online publication, December 24, 2015; 10.1038/gt.2015.113

Abstract | Full Text

Efficacy and safety of myocardial gene transfer of adenovirus, adeno-associated virus and lentivirus vectors in the mouse heart

M Merentie, L Lottonen-Raikaslehto, V Parviainen, J Huusko, S Pikkarainen, M Mendel, N Laham-Karam, V Kärjä, R Rissanen, M Hedman and S Ylä-Herttuala

Gene Ther 2016 23: 296-305; advance online publication, December 24, 2015; 10.1038/gt.2015.114

Abstract | Full Text

Safety and efficacy of plasmid DNA expressing two isoforms of hepatocyte growth factor in patients with critical limb ischemia

M R Kibbe, A T Hirsch, F O Mendelsohn, M G Davies, H Pham, J Saucedo, W Marston, W-B Pyun, S-K Min, B G Peterson, A Comerota, D Choi, J Ballard, R A Bartow, D W Losordo, W Sherman, V Driver and E C Perin

Gene Ther 2016 23: 306-312; advance online publication, December 8, 2015; 10.1038/gt.2015.110

Abstract | Full Text

Short Communication

Top

Prevalence of AAV1 neutralizing antibodies and consequences for a clinical trial of gene transfer for advanced heart failure

B Greenberg, J Butler, G M Felker, P Ponikowski, A A Voors, J M Pogoda, R Provost, J Guerrero, R J Hajjar and K M Zsebo

Gene Ther 2016 23: 313-319; advance online publication, December 24, 2015; 10.1038/gt.2015.109

Abstract | Full Text

Corrigendum

Top

Efficient delivery of lentiviral vectors into resting human CD4 T cells

X Geng, G Doitsh, Z Yang, N L K Galloway and W C Greene

Gene Ther 2016 23: 320-322; 10.1038/gt.2015.115

Full Text

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