Xiao Xiao

发表

Myostatin propeptide gene delivery by adeno-associated virus serotype 8 vectors enhances muscle growth and ameliorates dystrophic phenotypes in mdx mice.

Juan Li, Bing Wang, Xiaodong Zhu, 2008, Human gene therapy.

Effective rescue of dystrophin improves cardiac function in dystrophin-deficient mice by a modified morpholino oligomer

P. Iversen, H. Moulton, Juan Li, 2008, Proceedings of the National Academy of Sciences.

An engineered serum albumin-binding AAV9 capsid achieves improved liver transduction after intravenous delivery in mice

Juan Li, C. Qiao, Jianbin Li, 2019, Gene Therapy.

Post-Natal Knockdown of Fukutin-Related Protein Expression in Muscle by Long-Term RNA Interference Induces Dystrophic Pathology

Juan Li, Peijuan Lu, Q. Lu, 2011 .

GRAF1 promotes ferlin-dependent myoblast fusion.

E. McNally, Joan M. Taylor, C. Mack, 2014, Developmental biology.

GRAF1 deficiency blunts sarcolemmal injury repair and exacerbates cardiac and skeletal muscle pathology in dystrophin-deficient mice

E. McNally, Joan M. Taylor, C. Mack, 2015, Skeletal Muscle.

Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies

Eric P. Hoffman, Zheng Fan, Xiao Xiao, 2012, Mammalian Genome.

A GDF11/myostatin inhibitor, GDF11 propeptide-Fc, increases skeletal muscle mass and improves muscle strength in dystrophic mdx mice

Juan Li, C. Qiao, Jianbin Li, 2019, Skeletal Muscle.

Adeno-associated virus vector-mediated gene transfer into dystrophin-deficient skeletal muscles evokes enhanced immune response against the transgene product

S. Takeda, Juan Li, J. Chamberlain, 2002, Gene Therapy.

Efficient long-term gene transfer into muscle tissue of immunocompetent mice by adeno-associated virus vector

R. Samulski, Juan Li, X Xiao, 1996, Journal of virology.

Role for highly regulated rep gene expression in adeno-associated virus vector production

R. Samulski, Juan Li, X. Xiao, 1997, Journal of virology.

Evaluation of an AAV9-mini-dystrophin gene therapy candidate in a rat model of Duchenne muscular dystrophy

J. Grieger, T. Larcher, Juan Li, 2023, Molecular therapy. Methods & clinical development.

Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model.

Juan Li, X. Xiao, J. Li, 2000, Proceedings of the National Academy of Sciences of the United States of America.

A canine minidystrophin is functional and therapeutic in mdx mice

L. Zhou, J. Kornegay, J. Bogan, 2008, Gene Therapy.

317. HH67.2, a Promising Novel Adeno-Associated Virus (AAV) Vector, Shows Improved Muscle Specificity and Infectivity Compared To AAV9

Juan Li, Christina Mayer, C. Martin, 2015 .

rAAV vector-mediated sarcogylcan gene transfer in a hamster model for limb girdle muscular dystrophy

D. Dressman, E. Hoffman, Y. Tsao, 1999, Gene Therapy.