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Description
This disorder is caused by an inherited deficiency of glutaryl-CoA dehydrogenase, which is involved in the catabolic pathways of L-lysine, L-hydroxylysine and L-tryptophan (97)

Mitochondrial preparations from C2C12 cells overexpressing FLAG-tagged full-length Alix were lysed with ice-cold lysis buffer (1 TBS [pH 8.0], 0.3% NP-40, 20% glycerol, 0.215 mM EDTA [pH 8.0], 150 mM KCl, protease inhibitors, and phosphatase inhibitors) by using a Dounce homogenizer (15 strokes)

Vitamin K supplementation can improve stability of anticoagulation for patients with unexplained variability in response to warfarin

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Peyronies disease is the formation of excess scar tissue in the penis, most commonly in the stucture known as the tunica albuginea

Endocrinology 155: 17081717, 2014
