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doi:10.1016/j.jep.2024.118963 118

CMA is a lysosome-dependent protein degradation process, during which LD coat proteins, perilipin 2 (PLP2) and perilipin 3 (PLP3), bounded by cytosolic heat shock-associated protein 70 (Hsc70), are imported into the lysosome through a lysosome-associated membrane protein (LAMP2A) and are degraded [82]

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Human SIGLEC7 isoform 1(NP _055200.1, the longest isoform) may be encoded by transcript variant 1(NM _ 014385.3)

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