An essential receptor for adeno-associated virus infection

In vivo genome editing using Staphylococcus aureus Cas9

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Engineering adeno-associated viruses for clinical gene therapy

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The role of cellular adhesion molecules in virus attachment and entry

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Lassa virus entry requires a trigger-induced receptor switch

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Selection and evaluation of clinically relevant AAV variants in a xenograft liver model

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Genome engineering using the CRISPR-Cas9 system

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A survey of ex vivo/in vitro transduction efficiency of mammalian primary cells and cell lines with Nine natural adeno-associated virus (AAV1-9) and one engineered adeno-associated virus serotype

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Gene therapy for lipoprotein lipase deficiency

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A transcription activator-like effector toolbox for genome engineering

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Adeno-Associated Virus 2 Infection Requires Endocytosis through the CLIC/GEEC Pathway

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Endocytic sorting of transmembrane protein cargo

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Antibody-based protection against HIV infection by vectored immunoprophylaxis

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Ebola virus entry requires the cholesterol transporter Niemann–Pick C1

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Recent Advances in Retromer Biology

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A theoretical molecular network for dyslexia: integrating available genetic findings

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Transport according to GARP: receiving retrograde cargo at the trans-Golgi network

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A Versatile Viral System for Expression and Depletion of Proteins in Mammalian Cells

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Analysis of AAV Serotypes 1–9 Mediated Gene Expression and Tropism in Mice After Systemic Injection

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