Results 51 to 60 of about 176,145 (169)
Glycogen Granules Are Degraded by Non-Selective Autophagy in Nitrogen-Starved Komagataella phaffii
Autophagy was initially recognized as a bulk degradation process that randomly sequesters and degrades cytoplasmic material in lysosomes (vacuoles in yeast). In recent years, various types of selective autophagy have been discovered.
Nimna V. Wijewantha +2 more
doaj +1 more source
Changes in the content of protein, glycogen, neutral lipids and sterols were investigated in locust eggs from oviposition until larval hatching. The content of all of these nutritional reserves was higher in the eggs of S.
Václav NĚMEC
doaj +1 more source
Influence of post-mortem muscle glycogen content on the quality of beef during aging
Introduction: Glycolic changes which occur post-mortem have an impact on the physical and sensory features of beef, which in turn determine the successive processes and influence such beef quality traits as colour, tenderness, and cooling loss.
Onopiuk Anna +2 more
doaj +1 more source
Autophagy of glycogen is non-selective in Komagataella phaffii
Glycogen is an important reserve polysaccharide from bacteria to human. It is organized in glycogen granules that also contain several proteins involved in their metabolism.
Taras Y. Nazarko
doaj +1 more source
Methods for detection of cardiac glycogen-autophagy
Glycogen-autophagy (‘glycophagy’) is a selective autophagy process involved in delivering glycogen to the lysosome for bulk degradation. Glycophagy protein intermediaries include STBD1 as a glycogen tagging receptor, delivering the glycogen cargo into ...
Parisa Koutsifeli +14 more
doaj +1 more source
Background: Impairment in metabolism of lipids, especially in liver tissue, is one of the main complications of type 2 diabetes (T2D). This study aimed to evaluate the effect of hydroalcoholic extract of Satureja avromanica (HESA) on glycogen and lipid ...
Seyed Mohammad Ali Malaekeh +2 more
doaj
Glycogen storage disease type III (GSDIII) is a hereditary glycogenosis caused by deficiency of the glycogen debranching enzyme (GDE), an enzyme, encoded by Agl, enabling glycogen degradation by catalyzing alpha-1,4-oligosaccharide side chain transfer ...
Kumudesh Mishra +11 more
doaj +1 more source
W D, Bancroft, G, Bancroft
openaire +2 more sources

