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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
4 egulating the blood-nerve barrier (including orosomucoid 1).
5 al pattern of liver overexpression for CD14, orosomucoid 1, hepcidin, Spi 2.1, Ith3, and Tim-44.
6              Chromosome 17q21, harboring the orosomucoid 1-like 3 (ORMDL3) gene, has been consistentl
7 lpha (TNFalpha) and the acute phase reactant orosomucoid-1 (ORM1).
8     Furthermore, current research identified Orosomucoid 2 (ORM2) in the liver as one of the mediator
9 res involved in the transport of derivatized orosomucoid (alpha1-acidic glycoprotein) across the cont
10 response and inflammatory markers, including orosomucoid, amyloid, metallothionein, Fas antigen, and
11 as demonstrated by flow cytometry using FITC-orosomucoid and FITC-BSA controls.
12      We identified the ORM1 gene, coding for orosomucoid, as a novel locus associated with lag time v
13  unlike H1, which can bind the ligand asialo-orosomucoid (ASOR) when overexpressed in COS-7 cells, H2
14 ied by affinity chromatography, using asialo-orosomucoid (ASOR)-, anti-H1-, or anti-H2-COOH-Sepharose
15    Our findings indicate that: (i) monomeric orosomucoid binds to the luminal surface of the endothel
16  supplementing normal plasma with increasing orosomucoid concentrations was associated with impaired
17 n was assessed by uptake of iodinated asialo-orosomucoid, immunoglobulin (Ig) A1, and haptocorrin.
18 l spaces; and (v) the vesicular transport of orosomucoid is strongly inhibited by N-ethylmaleimide (>
19                                              Orosomucoid like 3 (ORMDL3) has been strongly linked wit
20 cadherin-related family member 3 (CDHR3) and orosomucoid like 3 (ORMDL3), were elucidated.
21                                          The orosomucoid-like (ORMDL) protein family is involved in t
22                                              Orosomucoid-like (ORMDL)3 has been strongly linked with
23 lipid metabolism, particularly involving the orosomucoid-like 3 (ORMDL3) gene, have been associated w
24  SNPs on expression of the asthma-associated orosomucoid-like 3 gene (ORMDL3).
25 sk alleles positively correlate with ORMDL3 (orosomucoid-like 3) expression.
26 rphisms in the endoplasmic reticular protein orosomucoid-like protein 3 (ORMDL3), which regulates sph
27 wel disease have identified risk loci in the orosomucoid-like protein 3/ORMDL sphingolipid biosynthes
28                                              Orosomucoid-like proteins (ORMs) interact with serine pa
29  thaliana) putative SPT regulatory proteins, orosomucoid-like proteins AtORM1 and AtORM2, were found
30 or its intravascular administration; (iv) no orosomucoid molecules are found in the intercellular jun
31                                        Human orosomucoid (OM) was used as a representative AGP.
32 as used to modify alpha 1-acid glycoprotein (orosomucoid, OMD) under various conditions.
33 he glycoproteins asialoorosomucoid (AsOR) or orosomucoid (OR).
34 we provide evidence showing that Arabidopsis orosomucoid (ORM) proteins, which have been known to be
35                                              Orosomucoids (ORMs) have historically been considered as
36 h a molar ratio of 0.26 compared with asialo-orosomucoid; porcine haptocorrin bound with a molar rati
37 andidate IBD markers, C-reactive protein and orosomucoid protein, identified in a recent discovery ex
38 ncovered, increasing evidence has pointed to orosomucoid proteins (ORMs) playing a major regulatory r
39              Because, by size and shape, the orosomucoid qualifies as a preferential probe for the po
40 eptors, but SRCL binds selectively to asialo-orosomucoid rather than generally to asialoglycoproteins
41 metry as charge forms of 11 plasma proteins: Orosomucoid, transferrin, alpha-1 microglobulin, zinc al