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P.2terminal kinase as a mechanism for fumonisin B1 induced apoptosis in murine primary hepatocytes
LA-ICP-MS: Laser ablation - inductively coupled plasma - mass spectrometry LDL: Low-density lipoproteins MD: Menkes disease MNK1: Menkes protein (soluble cytosolic ATP7A domain) MT: Metallothionein -PIXE: Micro - particle induced X ray emission MS: Multiple sclerosis COMMD1: MURR1 domain protein 1 NMDA: N-methyl- D -aspartate PD: Parkinsons disease pAs: Polyamines PrP C : Prion protein, helical (Adgrg6 receptor agonist) PrP Sc : Prion protein, sheet enriched (scrapie) SPARC: Secreted protein, acidic and rich in cysteine STP: Source-target-physiology SVZ: Sub-ventricular zone TSPP: Tetrakis-(4-sulfophenyl)-porphine TM: Tetrathiomolybdate Trientine: TETA, Trien (Triethylene tetramine) WD: Wilsons disease XFM: X-ray fluorescence microscopy References Crichton RR, Pierre J-L

[3] The scientists note that results together suggest that myostatin suppresses both basal and IGF-1-stimulated proliferation of both WAT and BAT preadipocytes, actions that are again similar to those in muscle satellite cells. Receptor Grade IGF-1 LR3, due to its speculated stability, may potentially counteract Myostatin by activating MyoD, a muscle protein normally triggered through prolonged physical strain