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Spatial Proteomics Reveals Disturbances in Trafficking and Interactions Along the Secretory Pathway Upon Loss of Neuropathy-Associated TECPR2
28/28 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
8 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 28 checked references that resolve
resolves10.1126/science.aan6298
Lysosomal metabolomics reveals V-ATPase- and mTOR-dependent regulation of amino acid efflux from lysosomes
resolves10.1146/annurev-cellbio-111315-125016
Cargo Capture and Bulk Flow in the Early Secretory Pathway
resolves10.1146/annurev-biophys-070317-033259
Assembly of COPI and COPII Vesicular Coat Proteins on Membranes
resolves10.1111/cge.12730
<scp>WES</scp> in a family trio suggests involvement of <scp>TECPR2</scp> in a complex form of progressive motor neuron disease
resolves10.1016/j.devcel.2017.03.015
Crosstalk between the Secretory and Autophagy Pathways Regulates Autophagosome Formation
resolves10.1096/fj.201802722R
A novel mutation in
<i>SPART</i>
gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism
resolves10.1080/15548627.2020.1852727
Lysosomal targeting of autophagosomes by the TECPR domain of TECPR2
resolves10.1242/jcs.222083
GM130 and p115 play a key role in the organisation of the early secretory pathway during skeletal muscle differentiation
resolves10.1091/mbc.e13-07-0381
ER exit sites are physical and functional core autophagosome biogenesis components
resolves10.1136/jmedgenet-2018-105503
<i>SEC31A</i> mutation affects ER homeostasis, causing a neurological syndrome
resolves10.1016/j.ejpn.2015.10.003
TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability
resolves10.1074/mcp.RA118.000608
Click Chemistry-mediated Biotinylation Reveals a Function for the Protease BACE1 in Modulating the Neuronal Surface Glycoproteome
resolves10.1038/nprot.2016.018
Spatially resolved proteomic mapping in living cells with the engineered peroxidase APEX2
resolves10.1016/j.cell.2021.10.017
Mammalian hybrid pre-autophagosomal structure HyPAS generates autophagosomes
resolves10.1016/j.cell.2017.03.022
An Approach to Spatiotemporally Resolve Protein Interaction Networks in Living Cells
resolves10.1002/humu.24206
Clinical, neuroimaging, and molecular spectrum of
<i>TECPR2</i>
‐associated hereditary sensory and autonomic neuropathy with intellectual disability
resolves10.1016/j.ajhg.2012.09.015
Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis
resolves10.1007/s00439-015-1632-8
GOLGA2, encoding a master regulator of golgi apparatus, is mutated in a patient with a neuromuscular disorder
resolves10.1016/j.celrep.2018.07.081
Pathogenic TFG Mutations Underlying Hereditary Spastic Paraplegia Impair Secretory Protein Trafficking and Axon Fasciculation
resolves10.1080/15548627.2020.1852724
A tecpr2 knockout mouse exhibits age-dependent neuroaxonal dystrophy associated with autophagosome accumulation
resolves10.1038/nmeth.3901
The Perseus computational platform for comprehensive analysis of (prote)omics data
resolves10.1016/j.cell.2021.03.035
ER-to-Golgi protein delivery through an interwoven, tubular network extending from ER
resolves10.1016/j.molcel.2021.01.009
Systematically defining selective autophagy receptor-specific cargo using autophagosome content profiling
resolves10.1016/j.cub.2018.03.002
The ER Contact Proteins VAPA/B Interact with Multiple Autophagy Proteins to Modulate Autophagosome Biogenesis
The 8 references without a DOI — listed, not checked
no DOI — not checkedMaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification
no DOI — not checkedRemodeling of ER-exit sites initiates a membrane supply pathway for autophagosome biogenesis
no DOI — not checkedref11
no DOI — not checkedMultifaceted roles of COPII subunits in autophagy
no DOI — not checkedAn optimised version of the secretome protein enrichment with click sugars (SPECS) method leads to enhanced coverage of the secretome
no DOI — not checkedref28
no DOI — not checkedref33
no DOI — not checkedPathophysiological Significance of WDR62 and JNK Signaling in Human Diseases
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