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Description
Carnitine transporter mutations in Crohn's disease consists of missense mutation(s) in the gene coding plasma membrane transporter OCTN1 (SLC22A4) and/or mutation(s) in the promoter of the gene encoding OCTN2 (SLC22A5) [14,35]
Hier wurden einmal Personen auf eine Prvention von Leberschden untersucht und einmal nur 3 Frauen, die parenteral ernhrt wurden
L-carnitine and type II diabetes Insulin resistance, which plays an important role in the development of type II diabetes, could be related to a disruption of fatty acid oxidation in the muscle
National Institute of Child Health and Human Development Neonatal Research Network
This intricate calcium signaling cascade ultimately contributed to mitochondrial dysfunction and cell death
