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The adaptor protein chaperone AAGAB stabilizes AP-4 complex subunits

Molecular biology of the cell, 2022-10, Vol.33 (12), p.ar109-ar109

2022

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Altered distribution of ATG9A and accumulation of axonal aggregates in neurons from a mouse model of AP-4 deficiency syndrome

PLoS genetics, 2018-04, Vol.14 (4), p.e1007363-e1007363

2018

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Intrathecal AAV9/AP4M1 gene therapy for hereditary spastic paraplegia 50 shows safety and efficacy in preclinical studies

The Journal of clinical investigation, 2023-05, Vol.133 (10), p.1-16

2023

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Synaptic Vesicle Precursors and Lysosomes Are Transported by Different Mechanisms in the Axon of Mammalian Neurons

Cell reports (Cambridge), 2020-06, Vol.31 (11), p.107775-107775, Article 107775

2020

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Editorial: Intracellular trafficking and membrane dynamics in health and disease

Frontiers in molecular biosciences, 2024-07, Vol.11, p.1463093

2024

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Reversible association with motor proteins (RAMP): A streptavidin-based method to manipulate organelle positioning

PLoS biology, 2019-05, Vol.17 (5), p.e3000279-e3000279

2019

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Lysosomal Proteome and Secretome Analysis Identifies Missorted Enzymes and Their Nondegraded Substrates in Mucolipidosis III Mouse Cells

Molecular & cellular proteomics, 2018-08, Vol.17 (8), p.1612-1626

2018

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Prevalence of IgG antibodies against Malawi polyomavirus in patients with autoimmune diseases and lymphoproliferative disorders subjected to bone marrow transplantation

Frontiers in immunology, 2024-01, Vol.14, p.1293313

2024

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A human iPSC-derived inducible neuronal model of Niemann-Pick disease, type C1

BMC biology, 2021-10, Vol.19 (1), p.218-218, Article 218

2021

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AP-4 mediates export of ATG9A from the trans-Golgi network to promote autophagosome formation

Proceedings of the National Academy of Sciences - PNAS, 2017-12, Vol.114 (50), p.E10697-E10706

2017

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Phagocytosis: Phagolysosome vesiculation promotes cell corpse degradation

Current biology, 2023-02, Vol.33 (4), p.R143-R146

2023

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Autophagy in Myelinating Glia

The Journal of neuroscience, 2020-01, Vol.40 (2), p.256-266

2020

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BORC/kinesin-1 ensemble drives polarized transport of lysosomes into the axon

Proceedings of the National Academy of Sciences - PNAS, 2017-04, Vol.114 (14), p.E2955-E2964

2017

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Neuronal functions of adaptor complexes involved in protein sorting

Current opinion in neurobiology, 2018-08, Vol.51, p.103-110

2018

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Neuronal enhancers are hotspots for DNA single-strand break repair

Nature (London), 2021-05, Vol.593 (7859), p.440-444

2021

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The role of AP-4 in cargo export from the trans-Golgi network and hereditary spastic paraplegia

Biochemical Society transactions, 2020-10, Vol.48 (5), p.1877-1888

2020

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Human Mesenchymal Stem Cells and Innovative Scaffolds for Bone Tissue Engineering Applications

Tissue engineering. Part B, Reviews, 2023-10, Vol.29 (5), p.514-531

2023

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Osteosarcoma cell death induced by innovative scaffolds doped with chemotherapeutics

Journal of cellular physiology, 2024-05, Vol.239 (5), p.e31256-n/a

2024

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Messenger RNA transport on lysosomal vesicles maintains axonal mitochondrial homeostasis and prevents axonal degeneration

Nature neuroscience, 2024-06, Vol.27 (6), p.1087

2024

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Site-1 protease and lysosomal homeostasis

Biochimica et biophysica acta. Molecular cell research, 2017-11, Vol.1864 (11), p.2162-2168

2017

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Subunit interactions of the disease-related hexameric GlcNAc-1-phosphotransferase complex

Human molecular genetics, 2015-12, Vol.24 (23), p.6826-6835

2015

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Identification of the interaction domains between α‐ and γ‐subunits of GlcNAc‐1‐phosphotransferase

FEBS letters, 2016-12, Vol.590 (23), p.4287-4295

2016

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Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics

Brain (London, England : 1878), 2024-05, Vol.147 (5), p.1751-1767

2024

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Corrigendum to “The Reelin receptor ApoER2 is a cargo for the adaptor protein complex AP-4: Implications for hereditary spastic paraplegia” [Progr. Neurobiol. 234(2024)102575]

Progress in neurobiology, 2024-10, Vol.241, p.102662, Article 102662

2024

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Measurement of Lysosome Positioning by Shell Analysis and Line Scan

Methods in molecular biology (Clifton, N.J.), 2022, Vol.2473, p.285

2022

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The adaptor protein chaperone AAGAB stabilizes AP-4 complex subunits

Altered distribution of ATG9A and accumulation of axonal aggregates in neurons from a mouse model of AP-4 deficiency syndrome

Intrathecal AAV9/AP4M1 gene therapy for hereditary spastic paraplegia 50 shows safety and efficacy in preclinical studies

Synaptic Vesicle Precursors and Lysosomes Are Transported by Different Mechanisms in the Axon of Mammalian Neurons

Editorial: Intracellular trafficking and membrane dynamics in health and disease

Reversible association with motor proteins (RAMP): A streptavidin-based method to manipulate organelle positioning

Lysosomal Proteome and Secretome Analysis Identifies Missorted Enzymes and Their Nondegraded Substrates in Mucolipidosis III Mouse Cells

Prevalence of IgG antibodies against Malawi polyomavirus in patients with autoimmune diseases and lymphoproliferative disorders subjected to bone marrow transplantation

A human iPSC-derived inducible neuronal model of Niemann-Pick disease, type C1

AP-4 mediates export of ATG9A from the trans-Golgi network to promote autophagosome formation

Phagocytosis: Phagolysosome vesiculation promotes cell corpse degradation

Autophagy in Myelinating Glia

BORC/kinesin-1 ensemble drives polarized transport of lysosomes into the axon

Neuronal functions of adaptor complexes involved in protein sorting

Neuronal enhancers are hotspots for DNA single-strand break repair

The role of AP-4 in cargo export from the trans-Golgi network and hereditary spastic paraplegia

Human Mesenchymal Stem Cells and Innovative Scaffolds for Bone Tissue Engineering Applications

Osteosarcoma cell death induced by innovative scaffolds doped with chemotherapeutics

Messenger RNA transport on lysosomal vesicles maintains axonal mitochondrial homeostasis and prevents axonal degeneration

Site-1 protease and lysosomal homeostasis

Subunit interactions of the disease-related hexameric GlcNAc-1-phosphotransferase complex

Identification of the interaction domains between α‐ and γ‐subunits of GlcNAc‐1‐phosphotransferase

Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics

Corrigendum to “The Reelin receptor ApoER2 is a cargo for the adaptor protein complex AP-4: Implications for hereditary spastic paraplegia” [Progr. Neurobiol. 234(2024)102575]

Measurement of Lysosome Positioning by Shell Analysis and Line Scan

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