Results 101 to 110 of about 854 (122)

Vitamin D receptor signalling regulates the diet-driven metabolic shift during weaning. [PDF]

Mol Metab
Jawla N, Khare S, Yadav N, Nanda RK, Arimbasseri GA.   +4 more
europepmc   +1 more source

Dysfunction of astrocytic glycophagy exacerbates reperfusion injury in ischemic stroke. [PDF]

Redox Biol
Guo H, Li Y, Wang S, Yang Y, Xu T, Zhao J, Wang J, Zuo W, Wang P, Zhao G, Wang H, Hou W, Dong H, Cai Y.   +13 more
europepmc   +1 more source

The rapidly expanding role of LC3-interacting regions in autophagy. [PDF]

J Cell Biol
North BJ, Fracchiolla D, Ragusa MJ, Martens S, Shoemaker CJ.   +4 more
europepmc   +1 more source

Integrated multi-omics reveals the molecular mechanism of antibiotic-free Wenchang chicken (Gallus Gallus domesticus). [PDF]

Poult Sci
Zheng X, Gu L, Zhang X, Qi Y, Wu L, Shang Y, Wu F, Xu T, Chen A.   +8 more
europepmc   +1 more source

Glycogen Granules Are Degraded by Non-Selective Autophagy in Nitrogen-Starved Komagataella phaffii. [PDF]

Cells
Wijewantha NV, Kumar R, Nazarko TY.
europepmc   +1 more source

Expression changes of human Schlemm's canal endothelial cells in response to cyclic mechanical stretch. [PDF]

Exp Eye Res
Heo Y, Cai J, Perkumas K, Aboobakar IF, Stamer WD, Liu Y.   +5 more
europepmc   +1 more source

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Glycogen‐binding protein STBD1: Molecule and role in pathophysiology

Journal of Cellular Physiology, 2023
AbstractStarch‐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
exaly   +3 more sources

Proteomic analysis of clear cell foci in the human liver identifies differential expression of Starch-Binding Domain-Containing Protein 1 (STBD1)

Zeitschrift für Gastroenterologie, 2019
Antonio Cigliano, F Dombrowski, S Ribback   +2 more
exaly   +3 more sources

The effects of laforin, malin, Stbd1, and Ptg deficiencies on heart glycogen levels in Pompe disease mouse models

, 2015
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
openaire   +3 more sources