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Published in 2018 at "PLoS Genetics"
DOI: 10.1371/journal.pgen.1007363
Abstract: The hereditary spastic paraplegias (HSP) are a clinically and genetically heterogeneous group of disorders characterized by progressive lower limb spasticity. Mutations in subunits of the heterotetrameric (ε-β4-μ4-σ4) adaptor protein 4 (AP-4) complex cause an autosomal…
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Keywords:
model deficiency;
deficiency syndrome;
limb spasticity;
deficiency ... See more keywords
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Published in 2022 at "Cell reports"
DOI: 10.2139/ssrn.4009227
Abstract: ATG9A is a highly conserved membrane protein required for autophagy initiation. It is trafficked from the trans-Golgi network (TGN) to the phagophore to act as a membrane source for autophagosome expansion. Here, we show that…
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Keywords:
nondegradable ubiquitinated;
atg9a organizes;
ubiquitinated atg9a;
atg9a ... See more keywords