コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ere potent GLP-1 secretagogues (except kappa casein).
2 ein, 5 from alphaS2-casein, and 4 from kappa-casein.
3 ost 3.2 times more than A1A2 variant of beta-casein.
4 tection levels of 2microgmL(-1) for alpha-S1-casein.
5 ld not be detected from A2A2 variant of beta-casein.
6 e epitope in alphas1 -casein to 73% in kappa-casein.
7 ed, one from alphaS1-casein and 17 from beta-casein.
8 zed casein was negligible compared to native casein.
10 n (193-202), alphas1-casein (85-91), alphas1-casein (1-9), as well as alphas2-casein (189-197) have a
14 -casein, 4 from betaA2-casein, 4 from betaA3-casein, 25 from alphaS1-casein, 5 from alphaS2-casein, a
15 nt peptides; 74 of them originated from beta-casein, 4 from betaA2-casein, 4 from betaA3-casein, 25 f
16 m originated from beta-casein, 4 from betaA2-casein, 4 from betaA3-casein, 25 from alphaS1-casein, 5
17 asein, 4 from betaA3-casein, 25 from alphaS1-casein, 5 from alphaS2-casein, and 4 from kappa-casein.
19 Data for the baked cookies were as follows: casein, 84-90%; soy protein, 80-88%, and gluten, 80-90%.
20 sein (58-72), beta-casein (193-202), alphas1-casein (85-91), alphas1-casein (1-9), as well as alphas2
21 llowing recoveries based on soluble protein: casein, 95-107%; soy protein, 92-97%, and gluten, 96-99%
23 mount of each casein per allele was: alphas2-casein A = 2.9 +/- 0.8 g/L and F = 1.8 +/- 0.4 g/L; beta
27 f sodium caseinate (NaCN) and purified alpha-casein (alphas-CN) with an Aspergillus niger derived pro
28 hey proteins partially reassociated with the caseins, although a complex behaviour was observed at ap
29 f AI-ETD in localizing phosphosites in alpha-casein, an approximately 23.5 kDa phosphoprotein that sh
30 AcPs was preferentially active towards kappa-casein, analysed by Urea-PAGE and LC-ESI-MS, whereas the
32 diet with 20% casein (control group) or 15% casein and 5% of peptide fractions (treatment groups E1,
33 duplex ASV-QDs-based determination of bovine casein and bovine immunoglobulin G is carried out in mil
34 dissociation and the concentrations of kappa-casein and denatured whey protein in the serum, and a re
40 of milk and its major components, alpha/beta-casein and whey acidic protein (WAP), is significantly r
41 uman jejunal digests after oral ingestion of casein and whey protein were collected by a nasogastric
44 rgens (alphas1 -, alphas2 -, beta- and kappa-caseins and beta-lactoglobulin) in paired maternal and i
45 On acidification to pH 5.4, the serum phase caseins and denatured whey proteins partially reassociat
48 n this study, structural changes in micellar caseins and whey proteins due to high pressure--low temp
49 milk components (milk fat, xanthine oxidase, caseins and whey proteins) in pulsed electric field (PEF
50 quillaja saponin, Tween 80, whey protein and casein) and antioxidant type (EDTA, ascorbic acid, catec
51 t individual proteins (alpha, beta and kappa casein) and hydrolysates on an enteroendocrine cell line
52 n with enamel (e.g., compared with mucin and casein) and significantly reduced initial enamel erosion
54 , hemoglobin, bovine serum albumin, and beta-casein, and compare the results with enzymatic digestion
57 to enteroendocrine cells, and alpha and beta casein are particularly beneficial stimulating prolifera
58 ate with iron in the presence and absence of caseins are postulated, and new mechanisms are proposed.
60 d on the Michaelis-Menten plots, the Km with casein as substrate was 16.8muM and Vmax was 82.6muM/min
61 developed for allergens analysis using alpha-casein as the biomarker for cow's milk detection, to be
62 onstrated good selectivity towards the alpha-casein as the target analyte and adequate recoveries fro
64 during small-scale manufacture of semi-solid casein-based food matrices was investigated and found to
65 allow matrix formation during manufacture of casein-based food structures e.g. processed and analogue
66 n modulating hydration during manufacture of casein-based matrices than simply solubilising calcium o
67 main important result was obtained for kappa-casein because, till now, no data were available on quan
68 .9 +/- 0.8 g/L and F = 1.8 +/- 0.4 g/L; beta-casein C = 3.0 +/- 0.8 g/L and C1 = 2.0 +/- 0.7 g/L and
69 s2-casein genetic variants A and F, and beta-casein C and C1 with other previously described method.
72 isolate (WPI), soy protein isolate (SPI) and casein (CN) and their binary mixtures, viz., WPI+SPI, WP
73 k proteins, beta-lactoglobulin (beta-LG) and casein (CN) was greatly diminished with gastric simulati
76 S, whereas the degradation of alpha and beta-casein components by AcPs proceeded slowly justifying it
78 One PH formula and the EH formula containing casein components showed remaining IgE reactivity, where
80 re measured in rennet gels across a range of casein concentrations allowing to form networks of prote
81 ein:casein (WP:CN) ratios (with standardised casein concentrations) were made from powders produced b
83 ps of mice were fed a high-fat diet with 20% casein (control group) or 15% casein and 5% of peptide f
84 fed six protein diets for 14 days, including casein (control), and proteins isolated from soy, fish,
92 pH before heat treatment led to increases in casein dissociation and the concentrations of kappa-case
94 This study demonstrates and explains how casein-enriched retentates from microfiltration gel fast
96 mounts emptied faster than predominant whole casein feeds and one study found no difference in GE.
97 species of cytochrome C, lysozyme, and beta-casein formed during glycation with d-glucose were ident
98 administration of an extensively hydrolyzed casein formula (EHCF) containing the probiotic Lactobaci
100 hosphate and the aggregates consisted of all casein fractions, even at the lowest level of ferric chl
102 to be more efficiently digested compared to caseins from cow milk and peptide profiles from goat mil
104 The yield of BCM-7 (0.20+/-0.02mg/g beta-casein) from A1A1 variant was observed to be almost 3.2
105 id chromatographic (HPLC) method to quantify casein genetic variants (alphas2-, beta-, and kappa-case
106 was found between the quantities of alphas2-casein genetic variants A and F, and beta-casein C and C
108 as to evaluate the effect of the presence of casein glycomacropeptide (CMP) on the in vitro digestibi
109 tein group showed lower Grx1 levels than the casein group and the beef protein group showed the highe
112 ole of calcium chelating salts in modulating casein hydration and dispersion and gives an indication
113 Anti-inflammatory activity was observed in casein hydrolysate (CH) and pea protein hydrolysate (PPH
114 all cases) but entrapment was lower for the casein hydrolysate (circa 50%), possibly indicating a ph
116 fants were randomly assigned to groups fed a casein hydrolysate formula (n = 113) or a conventional f
117 ), whey protein isolate (WPI), insulin and a casein hydrolysate were entrapped in chitosan-polyphosph
121 tide, VLPVPQK (named peptide C) derived from casein hydrolysates was investigated along with extensiv
122 n these alternative hypotheses, we performed casein hydrolysis assays to measure the SpeB protease ac
123 The protease preparations displayed similar casein hydrolysis kinetics and were active in hydrolysin
124 e whey hydrolyzate (pHF-W, eHF-W), extensive casein hydrolyzate (eHF-C) or standard cow's milk formul
125 e sought to characterize immune responses to casein in children with FPIES caused by cow's milk (CM).
126 ess of the type of salt added, the amount of casein in milk serum decreased and the amount of calcium
127 tprandial chylomicron response compared with casein in persons with abdominal obesity, thereby indica
128 is hypothesised that the addition of iron to caseins in the presence of orthophosphate results in the
129 genetic variants (alphas2-, beta-, and kappa-casein) in milk of homozygous individuals of Girgentana
132 s, C2C12 myoblasts and 3T3-L1 adipocytes and casein injection in C57BL/6J mice to induce inflammatory
133 and hyperlipidemia regardless of exposure to casein injection, only the HFD+Casein mice showed increa
134 study evaluated the effects of intact whole casein, intact individual proteins (alpha, beta and kapp
135 food proteins, such as beta-lactoglobulin or caseins, intensely studied for bioactive peptide product
137 entrations of orthophosphate solution to the casein-iron precipitates resulted in gradual adsorption
142 g peptide, we established a pivotal role for casein kinase (CK)-2-mediated circadian BMAL1-Ser90 phos
144 ubiquitylation were blocked by disruption of casein kinase 1 (CK1) activity, and mass spectrometry an
145 such as phosphorylation of clock proteins by casein kinase 1 (CK1) and glycogen synthase kinase 3 (GS
148 protein stability of FOXO3A is regulated by Casein Kinase 1 alpha (CK1alpha) in an oncogenic RAS-spe
152 clock, a protein complex of frequency (FRQ), casein kinase 1a (CK1a), and the FRQ-interacting RNA Hel
153 t lenalidomide induces the ubiquitination of casein kinase 1A1 (CK1alpha) by the E3 ubiquitin ligase
154 and metastasis in vivo via downregulation of casein kinase 1alpha (CK1alpha), a suppressor of pro-met
156 nhibitor), adenomatous polyposis coli (APC), casein kinase 1alpha (CK1alpha), and glycogen synthase k
157 inc finger proteins 1 (IKZF1) and 3 (IKZF3), casein kinase 1alpha (CK1alpha), and the translation ter
158 IFN in the context of intestinal knockout of casein kinase 1alpha (CK1alpha), which controls the ubiq
159 mor suppressor adenomatous polyposis coli or casein kinase 1alpha uncovered new regulatory features a
162 ermined whether pharmacological targeting of casein kinase 1delta and epsilon (CK1delta/epsilon), key
166 earing a short-period mutation in the enzyme casein kinase 1epsilon (tau mutation), which accelerates
167 Here, we show that fission yeast Cki3 (a casein kinase 1gamma homolog) is a critical regulator to
168 es with thapsigargin (10 mum), inhibition of casein kinase 2 (4,5,6,7-tetrabromobenzotriazole; 10 mum
171 7 -: tetrabromobenzotriazole (TBB), a potent casein kinase 2 (CK2) inhibitor, as a strong suppressor
175 Previous in vitro studies indicated that casein kinase 2 (CK2) mediated the phosphorylation of NS
177 The MRE11-PIH1D1 interaction is dependent on casein kinase 2 (CK2) phosphorylation of two acidic sequ
178 The Foxc2 amino terminus has a consensus casein kinase 2 (CK2) phosphorylation site at serine 124
179 and overexpression experiments, we show that casein kinase 2 (CK2) promotes stress granule dynamics.
180 ctivated through pharmacologic inhibition of casein kinase 2 (CK2) to eradicate disease in high-risk
181 ere, we report that Brg1 is also a target of casein kinase 2 (CK2), a serine/threonine kinase, in pro
182 wn previously to require the Cka2 subunit of casein kinase 2 (CK2), a ubiquitous enzyme with multiple
183 on was dependent on XRCC1 phosphorylation by casein kinase 2 (CK2), enhancing XRCC1's interaction wit
184 on events catalyzed first by MEK and then by casein kinase 2 (CK2), followed by interaction with impo
185 e, and this phosphorylation was catalyzed by casein kinase 2 (CK2), the levels of which were dramatic
189 posttranslationally regulated by TNF-induced casein kinase 2 catalytic subunit (CK2alpha') phosphoryl
195 overed that murine Arl13b is a substrate for casein kinase 2, a contaminant in our preparation from h
196 ation of ErbB2 or loss of the betasubunit of casein kinase 2, shifted the whole population toward a f
197 uired Rab11-dependent trafficking and FAM20C/casein kinase 2-dependent C-terminal phosphorylation of
198 required for insulin induction of Sort1 in a casein kinase 2-dependent manner and that inhibition of
200 e U.S. Food and Drug Administration-approved casein kinase activator, pyrvinium) in C57Bl/6J mice res
203 When HOPS is phosphorylated by the vacuolar casein kinase I, Yck3p, tethering only takes place when
204 Set8 for ubiquitination and degradation in a casein kinase I-dependent manner, which is activated by
208 roaches, we have identified a novel role for casein kinase II (CKII) in the modification of the polym
210 s work, we show that Pah1 is a substrate for casein kinase II (CKII); its phosphorylation was time- a
211 this repression by directly interacting with Casein Kinase II and preventing it from activating HDAC3
213 ously reported that the protein kinase C and casein kinase II substrate in neurons (PACSIN) forms a c
214 In this study, we determined the role of casein kinase-1 (CK1) in regulating NMDAR activity in th
219 liver nuclei all three PERs, both CRYs, and Casein Kinase-1delta (CK1delta) are present together in
221 s NMDA receptor activity by interacting with casein kinase-2 and protein phosphatases in the hypothal
225 nase ataxia-telangiectasia-mutated (ATM) and casein kinase1 (CK1) and casein kinase2 (CK2) positively
226 a-mutated (ATM) and casein kinase1 (CK1) and casein kinase2 (CK2) positively and negatively regulates
233 isolate (WPI) solutions as well as micellar casein (MC) dispersions and mixtures were treated at 500
234 noblends were synthesized to detect micellar casein (MC), the main milk protein and an indicator of m
235 f exposure to casein injection, only the HFD+Casein mice showed increased hepatic vacuolar degenerati
237 tein with the casein micelle, an increase in casein micelle size, and reductions in concentrations of
238 sociation of denatured whey protein with the casein micelle, an increase in casein micelle size, and
239 was not different for vitamin D-re-assembled casein micelles and control fortified milks after 21days
240 erstand the physicochemical modifications of casein micelles induced by Ser2 and to confirm its impli
241 min D was retained in vitamin D-re-assembled casein micelles than control powders during storage, whi
243 fat-soluble vitamin loading in re-assembled casein micelles, and to evaluate vitamin D stability of
246 s markedly defective in cleaving bovine beta-casein or the natural CTRC substrates human cationic try
247 (P = 0.034), beta-lactoglobulin (P = 0.010), casein (P = 0.047) and lactoferrin (P = 0.030) during tr
249 in-derived peptides have shown that the beta-casein peptide (193-209) exhibits immunomodulatory, anti
251 new system was applied for the enrichment of casein phosphopeptides from a simulated tryptic digest w
252 ial of iron fortified goat and cow milks and casein phosphopeptides obtained from each species of mil
253 old sensor chip was used to immobilise alpha-casein-polyclonal antibody using EDC/NHS coupling proced
258 vitro gastric digestion behavior of whey and casein proteins in a heat-treated semisolid real food.
259 s less phosphorus and potassium than soy and casein proteins, as a supplemental protein source for MH
261 moieties were observed for lysozyme and beta-casein, respectively in various heating conditions.
269 il CD63 expression and histamine release and casein-specific CD4(+) regulatory T-cell proliferation.
272 low levels of CM and casein-specific IgG and casein-specific IgG4 in patients with CM-FPIES versus th
273 ion of IL-10 and higher secretion of IL-9 by casein-stimulated T cells were found in patients with CM
274 response and TH2 cytokines production after casein stimulation in children with CM-FPIES, results we
278 were more resistant to pepsin digestion than caseins; this is related with a higher satiety capacity.
281 ics and were active in hydrolysing BODIPY-FL casein to varying extents at postmortem aging meat pH (5
284 mic this dynamic passivation mechanism, beta-casein was encapsulated into GUVs, yielding a stable, hi
288 ling revealed that the AcPs activity on milk casein was similar to that of a commercial milk coagulan
289 imal loading of vitamin D (1.38-1.46mg/100mg casein) was found at 4.9mM phosphate, 4.0mM citrate and
291 s from bovine beta-lactoglobulin and alphaS1 casein were identified as suitable peptide markers of mi
292 o protein isolates; bovine serum albumin and casein were investigated for their available lysine cont
295 d enteroendocrine cell proliferation and all caseins were potent GLP-1 secretagogues (except kappa ca
297 fraction B of A1A1 and A1A2 variants of beta-casein with elastase and leucine aminopeptidase revealed
298 Milks with a wide range of whey protein:casein (WP:CN) ratios (with standardised casein concentr
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。