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Cell Death in Skeletal Muscle Diseases: Diverse Roles and Pathological Processes. [PDF]
Yang YL, Guo L.
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AlphaFold2 SLiM screen for LC3-LIR interactions in autophagy. [PDF]
Stuke JFM, Hummer G.
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Establishment of a placental lncRNA-mRNA expression network for early-onset preeclampsia. [PDF]
Chen Y +5 more
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Vitamin D receptor signalling regulates the diet-driven metabolic shift during weaning. [PDF]
Jawla N +4 more
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Glycogen‐binding protein STBD1: Molecule and role in pathophysiology
Journal of Cellular Physiology, 2023AbstractStarch‐binding domain‐containing protein 1 (STBD1) is a glycogen‐binding protein discovered in skeletal muscle gene differential expression that is pivotal to cellular energy metabolism. Recent studies have indicated that STBD1 is involved in many physiological processes, such as glycophagy, glycogen accumulation, and lipid droplet formation ...
Linxi Chen
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Indiana University-Purdue University Indianapolis (IUPUI)%%%%Pompe disease (PD) is a rare metabolic myopathy characterized by loss of acid alpha-glucosidase (GAA), the enzyme responsible for breaking down glycogen to glucose within the lysosomes. PD cells accumulate massive quantities of glycogen within their lysosomes, and as such, PD is classified as
Conway, Betsy Ann
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Unravelling the molecular role of STBD1 in Hepatocytes: A Focus on Protein-Protein Interactions.
Zeitschrift Fur GastroenterologieChristoph Metzendorf, Frank Dombrowski
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A small portion of cellular glycogen is transported to and degraded in lysosomes by acid α-glucosidase (GAA) in mammals, but it is unclear why and how glycogen is transported to the lysosomes.
Priya Kishnani +2 more
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The glycogen cargo receptor STBD1: from biology to disease targeted therapies
2022Glycophagy is a novel selective autophagy characterized by glycogen degradation via the lysosomal enzyme acid α-glucosidase (GAA). Starch-binding domain-containing protein 1 (STBD1) is a glycogen cargo receptor that mediates glycophagy through binding glycogen transport into lysosomes.
Qiannan Tang +3 more
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