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Curtis M Chan

Researcher at Charles River Laboratories

Publications -  6
Citations -  1651

Curtis M Chan is an academic researcher from Charles River Laboratories. The author has contributed to research in topics: Spinal muscular atrophy & Spinal cord. The author has an hindex of 4, co-authored 5 publications receiving 1453 citations.

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Intravascular AAV9 preferentially targets neonatal neurons and adult astrocytes

TL;DR: It is shown that adeno-associated virus (AAV) 9 injected intravenously bypasses the BBB and efficiently targets cells of the central nervous system (CNS) and may enable the development of gene therapies for a range of neurodegenerative diseases.
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Systemic Gene Delivery in Large Species for Targeting Spinal Cord, Brain, and Peripheral Tissues for Pediatric Disorders

TL;DR: CSF injection efficiently targeted motor neurons, and restricted gene expression to the CNS, providing an alternate delivery route and potentially lower manufacturing requirements for older, larger patients, and support the use of AAV9 for gene transfer to the central nervous system for disorders in pediatric populations.
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Use of tissue cross-reactivity studies in the development of antibody-based biopharmaceuticals: history, experience, methodology, and future directions.

TL;DR: Tissue cross-reactivity studies are screening assays recommended for antibody and antibody-like molecules that contain a complementarity-determining region (CDR), primarily to identify off- target binding and, secondarily, to identify sites of on-target binding that were not previously identified.
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Biodistribution of adeno-associated virus type-2 in nonhuman primates after convection-enhanced delivery to brain.

TL;DR: This study further validates convection-enhanced delivery (CED) as the preferred method of viral vector delivery to the brain, and supports a Phase I clinical testing of AAV2-hAADC in humans with Parkinson's disease.
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Detection of Higher Cycle Threshold Values in Culturable SARS-CoV-2 Omicron BA.1 Sublineage Compared with Pre-Omicron Variant Specimens — San Francisco Bay Area, California, July 2021—March 2022

TL;DR: Data show that Ct values likely do not provide a consistent proxy for infectiousness across SARS-CoV-2 variants, and among specimens with culturable virus detected, Ct values were higher during Omicron BA.1.1 infections than during pre-Omicron infections, suggesting variant-specific differences in viral dynamics.