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8/15/2019 prx2
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Comparative analysis of Prx1 and Prx2 expression in mice provides evidence for incomplete compensation
cba.musc. viewPUBLICATIONS: Original Research Articles: Norris RA and Kern MJ. Functional characterization of domains important for transcriptional regulation by Prx1 and Prx2 homeoproteins. Molecular Biology of the Cell 10S:p96:556 1999
Crystal field splittings of PrX2 compounds (X=Pt, Rh, Ir, Ru, Ni) studied by inelastic neutron scattering
Prx1 and Prx2 cooperatively regulate the morphogenesis of the medial region of the mandibular process
Down-regulation of MAPK/NF-κB signaling underlies anti-inflammatory response induced by transduced PEP-1-Prx2 proteins in LPS-induced Raw 264.7 and TPA-induced mouse ear edema model
Signaling pathways regulating the expression of Prx1 and Prx2 in the chick mandibular mesenchyme
Hyperfine specific heats of PrX2 (X = Ir, Pt, Rh, Ru) laves phase compounds
GeneChip Microarrays Facilitate Identification of Protease Nexin-1 as a Target Gene of the Prx2 (S8) Homeoprotein
Magnetic properties of PrX2 compounds (X = Pt, Rh, Ru, Ir) studied by hyperfine specific heat, magnetization and neutron-diffraction measurements
Specific heat, resistivity, and AC susceptibility of the cubic PrX2 compounds (X = Pt, Ru, Ir, Rh)
Analytical results for crystalline electric field eigenvalues of trivalent rare-earth ions using computer algebra: application to the magnetism of PrX2 (X = Mg, Al, Ru, Rh, Pt)