scAAV9 intracisternal delivery results in efficient gene transfer to the central nervous system of a feline model of motor neuron disease.
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High resolution MRI anatomy of the cat brain at 3 Tesla.Intracisternal delivery of NFκB-inducible scAAV2/9 reveals locoregional neuroinflammation induced by systemic kainic acid treatment.Widespread and efficient transduction of spinal cord and brain following neonatal AAV injection and potential disease modifying effect in ALS mice.Enzyme replacement in the CSF to treat metachromatic leukodystrophy in mouse model using single intracerebroventricular injection of self-complementary AAV1 vectorAAV9-mediated central nervous system-targeted gene delivery via cisterna magna route in mice.Intrathecal administration of AAV/GALC vectors in 10-11-day-old twitcher mice improves survival and is enhanced by bone marrow transplantPlastin-3 extends survival and reduces severity in mouse models of spinal muscular atrophy.Novel Vector Design and Hexosaminidase Variant Enabling Self-Complementary Adeno-Associated Virus for the Treatment of Tay-Sachs Disease.Gene-based therapies of neuromuscular disorders: an update and the pivotal role of patient organizations in their discovery and implementation.Preclinical toxicity evaluation of AAV for pain: evidence from human AAV studies and from the pharmacology of analgesic drugs.Trans-neuronal transduction of spinal neurons following cortical injection and anterograde axonal transport of a bicistronic AAV1 vectorClinical Improvement of Alpha-mannosidosis Cat Following a Single Cisterna Magna Infusion of AAV1.Gene therapy and peripheral nerve repair: a perspective.Intracisternal delivery of AAV9 results in oligodendrocyte and motor neuron transduction in the whole central nervous system of cats.AAV9-NPC1 significantly ameliorates Purkinje cell death and behavioral abnormalities in mouse NPC disease.Long-term neurologic and cardiac correction by intrathecal gene therapy in Pompe disease.Efficient central nervous system AAVrh10-mediated intrathecal gene transfer in adult and neonate rats.Motor Neuron Gene Therapy: Lessons from Spinal Muscular Atrophy for Amyotrophic Lateral Sclerosis.AAV gene delivery to the spinal cord: serotypes, methods, candidate diseases, and clinical trials.Slow Infusion of Recombinant Adeno-Associated Viruses into the Mouse Cerebrospinal Fluid Space.
P2860
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P2860
scAAV9 intracisternal delivery results in efficient gene transfer to the central nervous system of a feline model of motor neuron disease.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
scAAV9 intracisternal delivery ...... model of motor neuron disease.
@en
scAAV9 intracisternal delivery ...... model of motor neuron disease.
@nl
type
label
scAAV9 intracisternal delivery ...... model of motor neuron disease.
@en
scAAV9 intracisternal delivery ...... model of motor neuron disease.
@nl
prefLabel
scAAV9 intracisternal delivery ...... model of motor neuron disease.
@en
scAAV9 intracisternal delivery ...... model of motor neuron disease.
@nl
P2093
P356
P1433
P1476
scAAV9 intracisternal delivery ...... model of motor neuron disease.
@en
P2093
Béatrice Joussemet
Delphine Briot-Nivard
Laurence Dubreil
Marie-Anne Colle
Martine Barkats
Maud Maquigneau
Philippe Moullier
Sandra Duque
Stéphanie Astord
P304
P356
10.1089/HUM.2012.218
P577
2013-07-01T00:00:00Z