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1 se signals represent meal-based responses to dietary protein.
2 alue in the occasional patient intolerant of dietary protein.
3 - 0.2 kg body weight during ED regardless of dietary protein.
4 h different glycemic indexes and contents of dietary protein.
5 protein and minerals and can be a source for dietary protein.
6 ted by insufficient or ineffectual intake of dietary protein.
7 nephron HCO(3) secretion that is induced by dietary protein.
8 ession of S phase proteins in the absence of dietary protein.
9 tion of daily energy, but not necessarily of dietary protein.
10 ge described for complexes of EGCG and other dietary proteins.
11 d be used as a supplement to poorly balanced dietary proteins.
12 o experiments to track the metabolic fate of dietary proteins.
13 derived from pathogens, microbial flora, or dietary proteins.
14 role in promoting tolerance of the flora and dietary proteins.
15 ly of resident salivary proteins but also of dietary proteins.
16 re pancreatic serine proteinases that digest dietary proteins.
17 cid intake that was higher by 4.72% of total dietary protein (2 SD) were -1.5 to -3.0 mm Hg systolic
19 d across membranes as an efficient route for dietary protein absorption and for maintaining cellular
21 study shows that the quantity and source of dietary proteins act as regulators of gut microbiota met
22 acterized a transient feeding preference for dietary protein after modest starvation in the fruit fly
23 e decreases suggests that the safe amount of dietary protein, although sufficient for maintenance of
26 d longitudinal associations between baseline dietary protein and bone mineral density (BMD) among 560
28 a finite element analysis, and we evaluated dietary protein and calcium with the use of a validated
31 udy was to determine the association between dietary protein and changes in total LM and nonbone appe
32 licited by chronically inadequate intakes of dietary protein and energy are affected by the protein c
39 nt for the potential influence of changes in dietary protein and mineral intake and risk factors for
42 ous non-carbonic acid production (NEAP) from dietary protein and potassium content enables exploratio
43 In 2 studies, we examined the ability of dietary protein and potassium to predict markers of bone
46 ctive was to examine the association between dietary protein and risk of IHD in a prospective study o
47 n have suggested an inverse relation between dietary protein and risk of ischemic heart disease (IHD)
48 bjective was to examine the relation between dietary protein and risk of stroke in men who participat
51 t growth and proliferation in the absence of dietary protein and thus uncouple neuroblasts from syste
53 se findings question the respective roles of dietary proteins and endogenous sources in generating si
54 ast growth factor 21 (FGF21) is regulated by dietary proteins and not, as has been heretofore assumed
57 est that CPO cleaves acidic amino acids from dietary proteins and peptides, thus complementing the ac
63 proteolysis, independent of energy status or dietary protein, as the activities of the 26S proteasome
64 is included participants who completed all 3 dietary protein assignments (61 for high SFA; 52 for low
71 ids affect the digestion and assimilation of dietary proteins by accelerating hydrolysis by pancreati
72 ody protein turnover and the contribution of dietary protein can be quantified in critically ill pati
73 nsume adequate or moderately high amounts of dietary protein can use RT to improve body composition,
74 d to determine the effect of graded doses of dietary protein co-ingested with carbohydrate on whole-b
75 We previously demonstrated that a common dietary protein component, wheat amylase trypsin inhibit
76 cterial richness tended to decrease when the dietary protein concentration reduced from 16% to 10%.
77 mous effects: mouse strain (A/J or C57BL/6), dietary protein content (14% protein and 0.3% L-cysteine
78 sions were efficiently corrected by lowering dietary protein content, and this was associated with tr
83 )) augments the postprandial availability of dietary protein-derived amino acids in the circulation a
84 )) augments the postprandial availability of dietary protein-derived amino acids in the circulation a
85 protein ingestion; however, incorporation of dietary protein-derived l-[1-13C]-phenylalanine into de
86 represent an important factor that modulates dietary protein digestion and absorption kinetics and th
88 e assessed the effect of meat texture on the dietary protein digestion rate, amino acid availability,
93 xamined the prospective association of novel dietary protein food clusters (derived from established
96 is given to the role of different sources of dietary protein (food vs. supplements) and non-protein n
97 simulated substitution of total and type of dietary protein for carbohydrate and of vegetable for an
98 his introduced alga as a potential source of dietary protein for human consumption in New Zealand.
101 ased oral exposure to chemicals compete with dietary proteins for the development of oral tolerance,
104 le-genome profiling revealed that increasing dietary protein from 5 to 40% increased duodenal transcr
105 nder practical dietary conditions, increased dietary protein from animal sources was not detrimental
107 his study examined the gastric hydrolysis of dietary protein from raw and roasted almonds in the grow
108 varied in main protein sources (60% of total dietary proteins from lean-seafood or nonseafood sources
109 postmenopausal women, a moderate increase in dietary protein, from 10% to 20% of energy, slightly imp
113 The response of this metabolic pathway to dietary protein (i.e., meal threshold) declines with adv
114 such as low glycemic index carbohydrates and dietary protein impact appetite, calorie intake and meta
116 sceptibility to infections; yet, the role of dietary protein in immune memory homeostasis remains poo
120 The findings show a metabolic requirement of dietary protein in sustaining functional CD8 memory and
124 nderlying negative responses to an excess of dietary protein, including the causes of the wasting syn
125 atically enhanced the proteolysis of several dietary proteins, including beta-lactoglobulin, bovine s
135 showed a significant association with higher dietary protein intake (effect per allele = 0.08 [0.06,
137 and meta-analysis evaluating the effects of dietary protein intake alone and with calcium with or wi
142 -increasing allele of FTO variant and higher dietary protein intake and offer insight into potential
143 uthors aimed to examine the relation between dietary protein intake and risk of cholecystectomy among
145 certain whether lower dietary acidity (lower dietary protein intake but higher potassium intake-ie, l
149 hat plasma glutathione turnover decreases as dietary protein intake decreases suggests that the safe
150 composition led to the hypothesis that high dietary protein intake derived from formula milk feeding
152 nciple trial to test whether manipulation of dietary protein intake during a marked energy deficit in
153 We examined the relation between maternal dietary protein intake during pregnancy and offspring an
154 l studies suggest that specifically maternal dietary protein intake during pregnancy influences child
160 ential benefits and challenges of optimizing dietary protein intake in older adults continues to evol
162 tudies have shown that more than half of the dietary protein intake is used by the gut and that a lar
165 y and suggest that interventions to optimize dietary protein intake may improve vaccine efficacy in m
166 controlling serum phosphorus by restricting dietary protein intake may outweigh the benefit of contr
169 e is currently no consensus on the effect of dietary protein intake on the skeleton, but there is som
175 pe of sex- and race-specific associations of dietary protein intake with 3- and 6-y changes in append
177 tary intake (particularly in caloric intake, dietary protein intake, dietary fiber intake, and micron
178 n proteasome system (UPS) response to varied dietary protein intake, energy deficit (ED), and consump
180 and stiffness of the peripheral skeleton and dietary protein intake, which is mainly related to chang
185 intakes (P-trend = 0.003), higher calibrated dietary protein intakes (P-trend = 0.03), higher aMED sc
186 load and stiffness, bone microstructure, and dietary protein intakes from various origins (animal, di
187 ed by areal bone mineral density (aBMD), and dietary protein intakes, particularly from specific diet
188 density (BMD) are positively correlated with dietary protein intakes, which account for 1-8% of BMC a
191 projected to increase global availability of dietary protein, iron, and zinc, these increases are mod
192 ood intake suggesting the perceived value of dietary protein is a critical determinant of its effect
195 odels.In a protein-replete cohort of adults, dietary protein is associated with ALM and QS but not wi
198 sults suggest that the requirement for total dietary protein is not different for healthy older adult
201 a function of drinking water, bulk diet, and dietary protein isotope ratios, explains >85% of the obs
202 The results indicate that, since LSPH is a dietary protein, it might possibly be formulated as a fu
203 males and females and juveniles derive their dietary protein largely from daily fruit and seasonal nu
205 tudy was conducted to investigate impacts of dietary protein levels on gut bacterial community and gu
207 ort the notion that modifying the sources of dietary protein may be potentially applied to prevent T2
209 .e. the precise macronutrient composition of dietary protein) may impact the effectiveness of weight
210 moderate increases in both cereal fibers and dietary protein (Mix diet) on insulin sensitivity, as me
213 set, and decreases in global availability of dietary protein of 2.9%, iron of 3.9%, and zinc of 3.4%
214 s in decreases in the global availability of dietary protein of 4.1%, iron of 2.8%, and zinc of 2.5%
215 stone disease are sparse, and the effects of dietary protein of different origins are not clear.
217 fication effects for intervention varying in dietary protein on 2-year changes in fat-free mass, whol
218 o determine the effects of varying levels of dietary protein on body composition and muscle protein s
220 despite intense investigation, the impact of dietary protein on calcium metabolism and bone balance r
221 The objective was to test the effect of dietary protein on calcium retention at low and high int
222 aluated the short-term effects of increasing dietary protein on Fe absorption and expression of genes
224 cts are largely driven by the impact of host dietary protein on host hemolymph (blood) osmolality (i.
226 te the effects of the quantity and source of dietary protein on microbiota composition, bacterial met
229 protein intake level and the food sources of dietary protein on the risk of ESRD in the general popul
231 for the first half of gestation of maternal dietary protein, or of total calorific intake on isolate
232 to our knowledge, we evaluate the effects of dietary protein (P), carbohydrate (C), fat (F), and ener
233 nificant negative correlations between total dietary protein (per kg) and markers of bone turnover (P
234 renal acid load (with an algorithm including dietary protein, phosphorous, potassium, magnesium, and
237 ifferences in the time of ingestion of daily dietary protein providing sulfate are related to the dev
241 studies using gnotobiotic mice revealed that dietary protein reduces the in vivo microbial metabolism
244 This study was designed to determine the dietary protein requirement of elderly women by using th
246 ose a framework for approaching the variable dietary protein requirements in patients with CKD or end
248 minated when urea excretion was decreased by dietary protein restriction (4% by weight), consistent w
249 in is necessary for the metabolic effects of dietary protein restriction and has more recently been p
250 d methylmalonic acidemia (MMA) is managed by dietary protein restriction and medical food supplementa
253 hepatic, genomic, and metabolic responses to dietary protein restriction in the non-pregnant Sprague-
257 GABAergic, neurons abrogated the effects of dietary protein restriction on reducing body weight, but
258 c neurons was dispensable for the effects of dietary protein restriction to increase insulin sensitiv
259 expenditure is a primary metabolic effect of dietary protein restriction, and requires both UCP1 and
260 that hepatic FGF21 expression is induced by dietary protein restriction, but not energy restriction.
267 nsiderable attention has recently focused on dietary protein's role in the mature skeleton, prompted
268 ts of "high versus low" protein intake or 2) dietary protein's synergistic effect with Ca+/-D intake
272 s experiencing increasing global demand as a dietary protein source and constituent of livestock feed
275 imate of the study site, adult age, sex, and dietary protein source on individual requirements; and t
276 f white meat to CVD risk, and the effects of dietary protein source on lipoprotein particle subfracti
279 as to elucidate the potentials of the 2 main dietary protein sources lean seafood and nonseafood to m
280 hensive and in-depth assessment of different dietary protein sources related to type 2 diabetes (T2D)
281 icant efforts are necessary to introduce new dietary protein sources to feed a growing world populati
283 zones of Bangladesh) of six prioritized key dietary protein sources: Oryza sativa (rice), Triticum a
286 ed trials (RCTs) investigating the effect of dietary protein supplementation during prolonged (>6 wk)
288 prudent to advise the intake of high-quality dietary protein to ensure adequate intakes of a number o
289 The recommendation to intentionally restrict dietary protein to improve bone health is unwarranted, a
290 c sulfur to urinary sulfate excretion and of dietary protein to urinary sulfate and nitrogen excretio
291 was developed to predict the potential of 72 dietary proteins to act as a source of dipeptidyl peptid
294 of nematodes by either limiting use of their dietary protein uptake from the crop or by preventing ro
296 ysosome-rich enterocytes (LREs), internalize dietary protein via receptor-mediated and fluid-phase en
297 cently, a more even mealtime distribution of dietary protein was positively associated with muscle ma
298 udy site, adult age class, sex, or source of dietary protein were observed, although there was an ind
299 mmunity-dwelling adults consume insufficient dietary protein, which may contribute to the age-related
300 topic and meta-analysis studies suggest that dietary protein works synergistically with calcium to im