PMID-sentid Pub_year Sent_text comp_official_name comp_offset protein_name organism prot_offset 20023138-1 2010 The objective of this investigation was to determine associations among rumen endotoxin, plasma serum amyloid A (SAA), and C-reactive protein (CRP) with plasma Ca, Fe, Zn, and Cu in lactating cows challenged with graded amounts of rolled barley grain in the diet (i.e., 0, 15, 30, and 45% of DMI). Iron 164-166 C-reactive protein Bos taurus 123-141 27457305-7 2016 The use of potassium dichromate and bronopol as preservatives in milk had no significant effects on milk Hp and M-SAA3 concentration but lowered milk CRP values compared to controls. Potassium Dichromate 11-31 C-reactive protein Bos taurus 150-153 27457305-7 2016 The use of potassium dichromate and bronopol as preservatives in milk had no significant effects on milk Hp and M-SAA3 concentration but lowered milk CRP values compared to controls. bronopol 36-44 C-reactive protein Bos taurus 150-153 26812328-12 2016 At 21 DOF, steers fed CrP had decreased glucose area under the curve (gAUC; = 0.01), decreased glucose clearance rate (; = 0.02), and increased glucose half-life (T; = 0.07) compared to steers fed Cont; however, by 98 DOF, no differences were observed between treatments. Glucose 40-47 C-reactive protein Bos taurus 22-25 26812328-12 2016 At 21 DOF, steers fed CrP had decreased glucose area under the curve (gAUC; = 0.01), decreased glucose clearance rate (; = 0.02), and increased glucose half-life (T; = 0.07) compared to steers fed Cont; however, by 98 DOF, no differences were observed between treatments. Glucose 95-102 C-reactive protein Bos taurus 22-25 26812328-12 2016 At 21 DOF, steers fed CrP had decreased glucose area under the curve (gAUC; = 0.01), decreased glucose clearance rate (; = 0.02), and increased glucose half-life (T; = 0.07) compared to steers fed Cont; however, by 98 DOF, no differences were observed between treatments. Glucose 95-102 C-reactive protein Bos taurus 22-25 26812328-12 2016 At 21 DOF, steers fed CrP had decreased glucose area under the curve (gAUC; = 0.01), decreased glucose clearance rate (; = 0.02), and increased glucose half-life (T; = 0.07) compared to steers fed Cont; however, by 98 DOF, no differences were observed between treatments. dof 6-9 C-reactive protein Bos taurus 22-25 26812328-15 2016 Results of this study indicate that CrP increased DP and tended to increase LM area but tended to decrease intramuscular fat, with no effect on growth performance. dp 50-52 C-reactive protein Bos taurus 36-39 20207160-1 2010 C-reactive protein (CRP) has been demonstrated to induce blood-brain barrier disruption (BBB) involving NAD(P)H-oxidase dependent oxidative stress. 1-((2-HYDROXYETHOXY)METHYL)-5-(3-(BENZYLOXY)BENZYL)-6-HYDROXYPYRIMIDINE-2,4(1H,3H)-DIONE 89-92 C-reactive protein Bos taurus 0-18 20023138-1 2010 The objective of this investigation was to determine associations among rumen endotoxin, plasma serum amyloid A (SAA), and C-reactive protein (CRP) with plasma Ca, Fe, Zn, and Cu in lactating cows challenged with graded amounts of rolled barley grain in the diet (i.e., 0, 15, 30, and 45% of DMI). Iron 164-166 C-reactive protein Bos taurus 143-146 20023138-1 2010 The objective of this investigation was to determine associations among rumen endotoxin, plasma serum amyloid A (SAA), and C-reactive protein (CRP) with plasma Ca, Fe, Zn, and Cu in lactating cows challenged with graded amounts of rolled barley grain in the diet (i.e., 0, 15, 30, and 45% of DMI). Zinc 168-170 C-reactive protein Bos taurus 143-146 20023138-1 2010 The objective of this investigation was to determine associations among rumen endotoxin, plasma serum amyloid A (SAA), and C-reactive protein (CRP) with plasma Ca, Fe, Zn, and Cu in lactating cows challenged with graded amounts of rolled barley grain in the diet (i.e., 0, 15, 30, and 45% of DMI). Copper 176-178 C-reactive protein Bos taurus 123-141 20023138-1 2010 The objective of this investigation was to determine associations among rumen endotoxin, plasma serum amyloid A (SAA), and C-reactive protein (CRP) with plasma Ca, Fe, Zn, and Cu in lactating cows challenged with graded amounts of rolled barley grain in the diet (i.e., 0, 15, 30, and 45% of DMI). Copper 176-178 C-reactive protein Bos taurus 143-146 15387799-11 2005 The protective effect of 10 microg/ml CRP on eNOS expression in TNF-alpha-incubated BAEC was prevented by an antibody against CD32 receptors. baec 84-88 C-reactive protein Bos taurus 38-41 20207160-1 2010 C-reactive protein (CRP) has been demonstrated to induce blood-brain barrier disruption (BBB) involving NAD(P)H-oxidase dependent oxidative stress. 1-((2-HYDROXYETHOXY)METHYL)-5-(3-(BENZYLOXY)BENZYL)-6-HYDROXYPYRIMIDINE-2,4(1H,3H)-DIONE 89-92 C-reactive protein Bos taurus 20-23 20207160-1 2010 C-reactive protein (CRP) has been demonstrated to induce blood-brain barrier disruption (BBB) involving NAD(P)H-oxidase dependent oxidative stress. NADP 104-109 C-reactive protein Bos taurus 0-18 20207160-1 2010 C-reactive protein (CRP) has been demonstrated to induce blood-brain barrier disruption (BBB) involving NAD(P)H-oxidase dependent oxidative stress. NADP 104-109 C-reactive protein Bos taurus 20-23 20207160-4 2010 Dichlorodihydrofluorescein measurements revealed significantly higher CRP-induced reactive oxygen species (ROS) levels in BEC. dichlorodihydrofluorescein 0-26 C-reactive protein Bos taurus 70-73 20207160-4 2010 Dichlorodihydrofluorescein measurements revealed significantly higher CRP-induced reactive oxygen species (ROS) levels in BEC. Reactive Oxygen Species 82-105 C-reactive protein Bos taurus 70-73 20207160-4 2010 Dichlorodihydrofluorescein measurements revealed significantly higher CRP-induced reactive oxygen species (ROS) levels in BEC. Reactive Oxygen Species 107-110 C-reactive protein Bos taurus 70-73 15310557-1 2004 C-reactive protein (CRP) and surfactant protein A (SP-A) are phosphatidylcholine (PC) binding proteins that function in the innate host defense system. Phosphatidylcholines 61-80 C-reactive protein Bos taurus 0-18 15310557-1 2004 C-reactive protein (CRP) and surfactant protein A (SP-A) are phosphatidylcholine (PC) binding proteins that function in the innate host defense system. Phosphatidylcholines 61-80 C-reactive protein Bos taurus 20-23 15310557-4 2004 The inhibitory effects of CRP were reversed by phosphorylcholine, a water-soluble CRP ligand. Phosphorylcholine 47-64 C-reactive protein Bos taurus 26-29 15310557-4 2004 The inhibitory effects of CRP were reversed by phosphorylcholine, a water-soluble CRP ligand. Phosphorylcholine 47-64 C-reactive protein Bos taurus 82-85 15310557-4 2004 The inhibitory effects of CRP were reversed by phosphorylcholine, a water-soluble CRP ligand. Water 68-73 C-reactive protein Bos taurus 26-29 15310557-4 2004 The inhibitory effects of CRP were reversed by phosphorylcholine, a water-soluble CRP ligand. Water 68-73 C-reactive protein Bos taurus 82-85 15310557-9 2004 These studies indicate that although SP-A and CRP both bind PC, there is a difference in the manner in which they interact with surface films. Phosphatidylcholines 60-62 C-reactive protein Bos taurus 46-49 14594250-2 2003 The influence of colostrum intake and the effect of additional lactulose application on the concentration of C-reactive protein (CRP) in blood were investigated. Lactulose 63-72 C-reactive protein Bos taurus 109-127 14594250-2 2003 The influence of colostrum intake and the effect of additional lactulose application on the concentration of C-reactive protein (CRP) in blood were investigated. Lactulose 63-72 C-reactive protein Bos taurus 129-132 9186778-2 1997 Further, the involvement of the mitochondrial adenine nucleotide translocase was examined by measuring CrP accumulation in mitochondria in the presence of substrates and inhibitors of the ATP/ADP-carrier and by investigating uptake kinetics in liposomes reconstituted with purified bovine heart adenine nucleotide translocase protein. Adenine Nucleotides 46-64 C-reactive protein Bos taurus 103-106 12760474-4 2003 Serum CRP was detected with sodium dodecyl sulfate polyacrylamide gel electrophoresis and western immunoblotting. Sodium Dodecyl Sulfate 28-50 C-reactive protein Bos taurus 6-9 12760474-4 2003 Serum CRP was detected with sodium dodecyl sulfate polyacrylamide gel electrophoresis and western immunoblotting. polyacrylamide 51-65 C-reactive protein Bos taurus 6-9 8807774-1 1996 The addition of C-reactive protein (CRP) to bovine platelets suspended in homologous plasma consistently produced a reversible aggregation response following stimulation with either platelet activating factor or adenosine diphosphate while untreated control samples exhibited irreversible aggregation. Adenosine Diphosphate 212-233 C-reactive protein Bos taurus 16-34 8807774-1 1996 The addition of C-reactive protein (CRP) to bovine platelets suspended in homologous plasma consistently produced a reversible aggregation response following stimulation with either platelet activating factor or adenosine diphosphate while untreated control samples exhibited irreversible aggregation. Adenosine Diphosphate 212-233 C-reactive protein Bos taurus 36-39 33984720-3 2021 Berberine treatment significantly reduced the LPS-induced expression levels of CRP, IL-1beta, IL-6, and TNF-alpha in bEECs. Berberine 0-9 C-reactive protein Bos taurus 79-82 2585927-2 1989 Affinity chromatography using HE agarose gel was the most effective method to isolate both CRP and SAP from a large volume of bovine serum. Helium 30-32 C-reactive protein Bos taurus 91-94 2585927-2 1989 Affinity chromatography using HE agarose gel was the most effective method to isolate both CRP and SAP from a large volume of bovine serum. Sepharose 33-40 C-reactive protein Bos taurus 91-94 34999217-9 2022 Finally, high-sensitivity C-reactive protein was significantly different among groups, as both the LPA group (4.8+-5.5 mg/L) and the MVPA group (3.5+-3.6 mg/L) had lower values (p<0.01) than the sedentary group (8.6+-8.4 mg/L). lpa 99-102 C-reactive protein Bos taurus 26-44 2585927-8 1989 Bovine CRP showed 23K dalton subunits by sodium laurylsulfate-PAGE and bovine SAP showed 28K and 32K dalton subunits, both of which were glycosylated and had identical amino acid compositions, indicating that both CRP and SAP molecules are pentamers. Sodium Dodecyl Sulfate 41-61 C-reactive protein Bos taurus 7-10 2981503-3 1985 Binding of double-stranded deoxyribopolynucleotides and calf thymus DNA by cAMP-CRP confers protection against attack by trypsin, subtilisin, S. aureus V8 protease, and clostripain. deoxyribopolynucleotides 27-51 C-reactive protein Bos taurus 80-83 2981503-3 1985 Binding of double-stranded deoxyribopolynucleotides and calf thymus DNA by cAMP-CRP confers protection against attack by trypsin, subtilisin, S. aureus V8 protease, and clostripain. Cyclic AMP 75-79 C-reactive protein Bos taurus 80-83 32118179-0 2020 Synthesis and Structural Optimization of Iridium(III) Solvent Complex for Electrochemiluminescence Labeling of Histidine-Rich Protein and Immunoassay Applications for CRP Detection. iridium(iii) 41-53 C-reactive protein Bos taurus 167-170 33360572-8 2021 Notably, beta-1,3-glucan markedly reduced serum levels of pro-inflammatory cytokines and C-reactive protein, while elevated serum immunoglobulin levels, indicating its immunity enhancement in transition cows. beta-1,3-glucan 9-24 C-reactive protein Bos taurus 89-107 30834110-9 2019 In NAA, S-HNL correlated negatively with PD20 (rho = - 0.048, p < 0.05) and CRP correlated negatively with mAQLQ (rho = - 0.439, p < 0.05). maqlq 110-115 C-reactive protein Bos taurus 79-82