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1 ecific uptake and degradation of 125I-asialo-orosomucoid.
2 ase genes such as serum amyloid proteins and orosomucoids.
3 igue, we found in rodent fatigue models that orosomucoid 1 (ORM1) was significantly increased in mult
8 res involved in the transport of derivatized orosomucoid (alpha1-acidic glycoprotein) across the cont
9 response and inflammatory markers, including orosomucoid, amyloid, metallothionein, Fas antigen, and
12 unlike H1, which can bind the ligand asialo-orosomucoid (ASOR) when overexpressed in COS-7 cells, H2
13 ied by affinity chromatography, using asialo-orosomucoid (ASOR)-, anti-H1-, or anti-H2-COOH-Sepharose
14 Our findings indicate that: (i) monomeric orosomucoid binds to the luminal surface of the endothel
15 supplementing normal plasma with increasing orosomucoid concentrations was associated with impaired
16 n was assessed by uptake of iodinated asialo-orosomucoid, immunoglobulin (Ig) A1, and haptocorrin.
17 l spaces; and (v) the vesicular transport of orosomucoid is strongly inhibited by N-ethylmaleimide (>
23 thaliana) putative SPT regulatory proteins, orosomucoid-like proteins AtORM1 and AtORM2, were found
24 or its intravascular administration; (iv) no orosomucoid molecules are found in the intercellular jun
28 h a molar ratio of 0.26 compared with asialo-orosomucoid; porcine haptocorrin bound with a molar rati
30 eptors, but SRCL binds selectively to asialo-orosomucoid rather than generally to asialoglycoproteins
31 metry as charge forms of 11 plasma proteins: Orosomucoid, transferrin, alpha-1 microglobulin, zinc al
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