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  2. Hypersomatotropism (veterinary) - Wikipedia

    en.wikipedia.org/wiki/Hypersomatotropism...

    The vast majority of cats present with diabetes mellitus, the possibility of hypersomatotropism causing it is rarely considered until the diabetes becomes difficult to control. In cats with difficult to control diabetes mellitus, hypersomatotropism should be considered as a cause only after exclusion of other conditions that can impact insulin.

  3. Diabetes in cats - Wikipedia

    en.wikipedia.org/wiki/Diabetes_in_cats

    Feline diabetes mellitus is a chronic disease in cats whereby either insufficient insulin response or insulin resistance leads to persistently high blood glucose concentrations. Diabetes affects up to 1 in 230 cats , [ 1 ] and may be becoming increasingly common.

  4. Chaperone-mediated autophagy - Wikipedia

    en.wikipedia.org/wiki/Chaperone-mediated_autophagy

    For instance, research with artificial CMA substrate showed that hsc70 chaperone binding to substrate or lysosomal binding does not necessarily require the substrate protein to be capable of unfolding, however, lysosomal translocation makes unfolding as a necessary criteria for it to be internalized. [3]

  5. Lysosome - Wikipedia

    en.wikipedia.org/wiki/Lysosome

    The lysosomal membrane protects the cytosol, and therefore the rest of the cell, from the degradative enzymes within the lysosome. The cell is additionally protected from any lysosomal acid hydrolases that drain into the cytosol, as these enzymes are pH-sensitive and do not function well or at all in the alkaline environment of the cytosol ...

  6. Lysosomal storage disease - Wikipedia

    en.wikipedia.org/wiki/Lysosomal_storage_disease

    Lysosomal storage disorders are caused by lysosomal dysfunction usually as a consequence of deficiency of a single enzyme required for the metabolism of lipids, glycoproteins (sugar-containing proteins), or mucopolysaccharides. Individually, lysosomal storage diseases occur with incidences of less than 1:100,000; however, as a group, the ...

  7. Autophagosome - Wikipedia

    en.wikipedia.org/wiki/Autophagosome

    Nonetheless, these structures contain endocytic markers even small lysosomal proteins such as cathepsin D. The process is similar in yeast, however the gene names differ. For example, LC3 in mammals is Atg8 in yeast and autophagosomes are generated from Pre-Autophagosomal Structure (PAS) which is distinct from the precursor structures in ...

  8. MAP1LC3B - Wikipedia

    en.wikipedia.org/wiki/MAP1LC3B

    MAP1LC3B is a member of the highly conserved ATG8 protein family. ATG8 proteins are present in all known eukaryotic organisms. The animal ATG8 family comprises three subfamilies: (i) microtubule-associated protein 1 light chain 3 (MAP1LC3); (ii) Golgi-associated ATPase enhancer of 16 kDa (GATE-16); and (iii) γ-amino-butyric acid receptor-associate protein ().

  9. Dysautonomia - Wikipedia

    en.wikipedia.org/wiki/Dysautonomia

    Dysautonomia, autonomic failure, or autonomic dysfunction is a condition in which the autonomic nervous system (ANS) does not work properly. This condition may affect the functioning of the heart , bladder , intestines , sweat glands , pupils , and blood vessels.