ライフサイエンスコーパス: digestive enzyme

1 encodes carboxyl ester lipase, a pancreatic digestive enzyme.

2 understanding of the effects of 2,4-DTBP on digestive enzyme.

3 in vivo pancreatic secretion and pancreatic digestive enzymes.

4 ality from impaired production of pancreatic digestive enzymes.

5 he compartment of the pancreas that produces digestive enzymes.

6 enzyme content resulted in poor secretion of digestive enzymes.

7 cretagogue stimulation with the secretion of digestive enzymes.

8 as recently been shown to involve pancreatic digestive enzymes.

9 d a significant portion of them are probably digestive enzymes.

10 normal postprandial synthesis of pancreatic digestive enzymes.

11 nitiating the activation of other intestinal digestive enzymes.

12 gut, the region responsible for secretion of digestive enzymes.

13 ol administration on pancreatic secretion of digestive enzymes.

14 wall porosity, by controlling the passage of digestive enzymes.

15 with the premature release and activation of digestive enzymes.

16 of developing type 2 diabetes by inhibiting digestive enzymes.

17 act nutrients from food by degradation using digestive enzymes.

18 e probably released from cell wall matrix by digestive enzymes.

19 iabetic peptides, which inhibit carbohydrate digestive enzymes.

20 ion, antioxidant activity, and inhibition of digestive enzymes.

21 y potentially improving the accessibility to digestive enzymes.

22 e used to investigate their capacity against digestive enzymes.

23 resulted in reduced starch susceptibility to digestive enzymes.

24 erential rates of processing by lepidopteran digestive enzymes.

25 oactive peptides that are liberated by human digestive enzymes.

26 The digestion was performed with and without digestive enzymes.

27 f phenolic interactions with proteins and/or digestive enzymes.

28 d prevented the activation of the cascade of digestive enzymes.

29 need to produce and secrete large amounts of digestive enzymes.

30 egraded by both the Lactobacillus strain and digestive enzymes.

31 plant biomass that is resistant to mammalian digestive enzymes.

32 gh bioaccessibility with slight influence of digestive enzymes.

33 al delivery system of molecules sensitive to digestive enzymes.

34 e, reducing growth of mice and production of digestive enzymes.

35 pancreatitis via intra-acinar activation of digestive enzymes.

36 ubmandibular gland function and secretion of digestive enzymes.

37 d to the production of very large amounts of digestive enzymes.

38 ty and exposing the pancreatic parenchyma to digestive enzymes.

39 , which normally prevents basal secretion of digestive enzymes.

40 for the body to excrete small molecules with digestive enzymes.

41 fic genes, including those for the secretory digestive enzymes.

42 ts increased after in vitro digestion due to digestive enzymes (4.6, 2.8 and 2.1, respectively).

43 dedicated to the production of the secretory digestive enzymes, a highly attuned surveillance of unfo

44 levated, including NPC1 and NPC2 and several digestive enzymes (acid lipase, beta-glucuronidase, and

45 cytoplasm where it can lead to intracellular digestive enzyme activation.

46 tracellular Ca(2+) homeostasis and premature digestive enzyme activation; however, the molecular mech

47 er understanding of pancreatic intracellular digestive enzyme activation; the pancreatic inflammatory

48 roxy for digestible food, under high and low digestive enzyme activities.

49 secretion and exposure of the parenchyma to digestive enzyme activity lead to organ damage and pancr

50 The benefits observed include enhanced digestive enzyme activity, improved intestinal integrity

51 participates in the regulation of intestinal digestive enzyme activity.

52 This may be a vital digestive enzyme adaptation allowing howler monkeys to s

53 ors (InsP(3)R) is the primary signal driving digestive enzyme and fluid secretion from pancreatic aci

54 holecystokinin (CCK) stimulates secretion of digestive enzyme and promotes cell growth, whereas acety

55 Despite the high lysosomal levels of digestive enzymes and acidity, the absorbed particles re

56 Despite the high lysosomal levels of digestive enzymes and acidity, the absorbed particles re

57 quences are less likely to be broken down by digestive enzymes and are thus more likely to be active

58 However, low pH in the stomach, various digestive enzymes and bile salts in the intestine threat

59 ce of CpCP3, which was highly susceptible to digestive enzymes and did not alter zebrafish embryos' m

60 ereas the chief cell predominantly expresses digestive enzymes and glycosylation-associated proteins.

61 epressing the expression of genes coding for digestive enzymes and larval cuticle proteins, while PAR

62 ange wines showed a reasonable inhibition of digestive enzymes and lipid peroxidation, twenty-one sam

63 Mutant mice had reduced serum levels of digestive enzymes and overall growth impairment.

64 In the host transcriptome, digestive enzymes and plastic degradation-related bacter

65 ine and endocrine cells control secretion of digestive enzymes and production of hormones to maintain

66 diverse ethnicity showed similar profiles of digestive enzymes and proteins involved in translation,

67 irectly induces expression of genes encoding digestive enzymes and secretory and mitochondrial protei

68 reduction in the synthesis of several major digestive enzymes and succumbs to massive apoptosis afte

69 Given the resistance of the oocyst wall to digestive enzymes and the ability of oocysts to cause pa

70 affect how accessible the substrates are to digestive enzymes and the gut microbiota.

71 ical conditions by adjusting factors such as digestive enzymes and their concentrations, pH levels, d

72 Different digestive enzymes and transporters are present in the du

73 onnections of dipeptidase 1 with circulating digestive enzymes and with hypertension.

74 isthorchis viverrini secrete growth factors, digestive enzymes, and extracellular vesicles (EVs) whic

75 opment, is not expressed and cells producing digestive enzymes are rare.

76 illustrates the multifaceted roles of insect digestive enzymes as mediators of plant-herbivore intera

77 n against attack from inflammatory cells and digestive enzymes, as well as against microbial infectio

78 d by changes in the content and secretion of digestive enzymes, as well as the phosphorylation of dow

79 ts the activity of enteropeptidase and other digestive enzymes at drug concentrations predicted to oc

80 factors revealed that Stammera encoded three digestive enzymes at the onset of symbiosis, including p

81 perty of flavonoids against mammalian starch digestive enzymes, because flavonoids interfere with com

82 ths at 18 degrees C), the genes encoding the digestive enzymes begin to be expressed as the female pr

83 d gut lactic acid bacteria and activities of digestive enzymes but did not show any antibiotic resist

84 nvolved in modulating the activity of starch digestive enzymes but remains unclear if their interacti

85 studied against both gastric and intestinal digestive enzymes but to different extents.

86 d in pancreatic acinar cells and encodes the digestive enzyme carboxyl ester lipase.

87 tablish a positive feedback mechanism in the digestive enzyme cascade of humans.

88 The digestive enzyme chymotrypsin protects the pancreas agai

89 om the left ventricle of adult rabbits using digestive enzymes (collagenase and protease).

90 ibited greater resistance to acid, heat, and digestive enzymes compared to erythritol glucosides (EG(

91 omplete digestive conditions, i.e. under low digestive enzyme concentrations.

92 regrowth of the pancreas but did not affect digestive enzyme content or secretory capacity.

93 ation of aberrant Ca2+ signaling and reduced digestive enzyme content resulted in poor secretion of d

94 of the Golgi apparatus and markedly reduced digestive enzyme content.

95 Here we show that digestive enzyme (DE) treatment of sporadic CJD brain ho

96 The digestive enzyme decreased the number of days with moder

97 the blunted increase of pancreatic and serum digestive enzymes during acute pancreatitis.

98 Rgs proteins inhibit the release of digestive enzymes evoked by G-protein-coupled-receptor a

99 This study investigated whether digestive enzyme expression in the duodenum and colon is

100 Digestive enzyme expression was only partially elevated

101 There are six digestive enzymes for starch: salivary and pancreatic al

102 red with symbiotic beetles supplemented with digestive enzymes from Stammera.

103 incorporation into mixed micelles, requiring digestive enzymes, gastric peristalsis, bile, and dietar

104 attributed to a profound down-regulation of digestive enzyme genes and trypsin activity, upon exposu

105 The magnitude of the effects on individual digestive enzyme genes correlated with the developmental

106 transcriptional activation of the secretory digestive enzyme genes.

107 Astacin, a crustacean digestive enzyme, has been proposed to carry out hydroly

108 D-amino acids can affect the action of digestive enzymes, hence the protein digestion.

109 ain body of the stomach, chief cells produce digestive enzymes; however, upon injury, they undergo ra

110 pancreatic inflammation, and intrapancreatic digestive enzyme (i.e., trypsinogen) activation.

111 Trypsin is best known as a digestive enzyme in animals, but remains unexplored in p

112 Trypsin is usually considered a digestive enzyme in the intestinal lumen.

113 ity of Lf is limited as it is susceptible to digestive enzymes in gastrointestinal tract.

114 The majority of digestive enzymes in humans are produced in the pancreas

115 as trypsin and chymotrypsin, are the primary digestive enzymes in lepidopteran larvae, and are also i

116 The exocrine pancreas secretes fluid and digestive enzymes in response to parasympathetic release

117 that control the physiological secretion of digestive enzymes in response to stimulation via the vag

118 njugates, can protect promastigotes from the digestive enzymes in the gut and, second, that LPG is re

119 Chymotrypsin is one of the most abundant digestive enzymes in the gut where it cleaves food prote

120 Thus, the presence of pancreatic digestive enzymes in the ischemic gut appears to be invo

121 examine here the hypothesis that pancreatic digestive enzymes in the ischemic intestine may be invol

122 The results indicate that pancreatic digestive enzymes in the ischemic intestine serve as an

123 the intracellular activation of proteolytic digestive enzymes in the pancreas and reduces the severi

124 (CCK) is known to stimulate the synthesis of digestive enzymes in the pancreas at the translational l

125 Premature activation of digestive enzymes in the pancreas has been linked to dev

126 ats, is to protect the parasite surface from digestive enzymes in the tsetse fly gut.

127 Trypsin and chymotrypsin, one of the major digestive enzymes in vertebrates, are pancreatic proenzy

128 ciency (PEI) reduces pancreatic secretion of digestive enzymes, including lipases.

129 ion enzymes and higher expression of general digestive enzymes, indicating the inability of larvae to

130 cts revealed potent antioxidant capacity and digestive enzyme inhibitory activity associated with the

131 tion to synthesize and directionally secrete digestive enzymes into a central lumen.

132 An array of digestive enzymes is incorporated into the cellulosome t

133 n experiences a decline in production of the digestive enzyme lactase-phlorizin hydrolase during matu

134 plains CTRC selectivity in regulating active digestive enzyme levels.

135 ies of antioxidant enzymes (SOD and CAT) and digestive enzymes (lipase, amylase and protease) were ob

136 Genetic mutations in pancreatic digestive enzymes may cause protein misfolding, endoplas

137 types specialized for the secretion of acid, digestive enzymes, mucus, and hormones.

138 n wheat ATI and two representative mammalian digestive enzymes, namely trypsin and alpha-amylase.

139 ted to producing the traps, attractants, and digestive enzymes needed for the carnivory.

140 s showed several changes in the behaviour of digestive enzymes, not only when the D-amino acids are i

141 ession (as much as 99%) of genes that encode digestive enzymes or proteins of regulated exocytosis an

142 ed proteins such as mucins (all tissues) and digestive enzymes (pancreas) in a soluble and/or inactiv

143 -toxic genotype with Alcalase as well as the digestive enzymes pepsin and pancreatin.

144 l, methylglyoxal and 2,3-butanedione and the digestive enzymes (pepsin and pancreatin) were studied.

145 rk the behaviour of the main stomach and gut digestive enzymes (pepsin, trypsin, and chymotrypsin) in

146 asmalemma, culminating in the release of the digestive enzyme pepsinogen into the lumina of gastric g

147 measured nitrogen isotope (delta(15) N) and digestive enzyme plasticity in four populations of sparr

148 Additionally, the presence of digestive enzymes positively contributed to antioxidant

149 adults consistently regulated genes encoding digestive enzymes, possibly to complement channel resist

150 Cells of the exocrine pancreas produce digestive enzymes potentially harmful to the intestinal

151 been reported in animal genomes, but are key digestive enzymes produced by wood-degrading fungi and s

152 models appear to recover via regeneration of digestive enzyme-producing acinar cells.

153 sphoglycans, which protect the parasite from digestive enzymes; production of chitinases that degrade

154 ystokinin octapeptide and reduced pancreatic digestive enzyme protein and mRNA levels, thus suggestin

155 ortant for the stimulation of translation of digestive enzyme protein in rat pancreas by CCK.

156 ute to the high specificity of CTRC-mediated digestive enzyme regulation.

157 r cell homeostasis required for secretion of digestive enzymes relies on SNARE-mediated exocytosis.

158 ivo and in vitro hydrolysis by human/porcine digestive enzymes, respectively, was examined.

159 terial pathogens from immune recognition and digestive enzymes secreted at the site of infection.

160 epithelial neck cell, the progenitor of the digestive enzyme secreting zymogenic (chief) cell (ZC).

161 sion of foveolar cells, and reprogramming of digestive enzyme-secreting chief cells into deep antral

162 astric epithelial mucous neck cells (NCs) to digestive enzyme-secreting zymogenic cells (ZCs) involve

163 Ca plays a central role in the control of digestive enzyme secretion and is largely mobilized from

164 s and prevented the pathologic inhibition of digestive enzyme secretion at supramaximal agonist conce

165 e the role of serine proteases in regulating digestive enzyme secretion in pancreatic acinar cells.

166 ed ethanol-induced stimulation of pancreatic digestive enzyme secretion may play a role in the events

167 Their GAP activity on digestive enzyme secretion was examined by adenovirus-me

168 ne trafficking events that are essential for digestive enzyme secretion.

169 3, p < .005), suggesting that the increased digestive enzyme-specific activity reflected differentia

170 Numerous studies have shown that GP2 binds digestive enzymes such as amylase, thereby supporting a

171 inin (CCK) plays an important role in normal digestive enzyme synthesis after feeding.

172 he signal transduction mechanisms regulating digestive enzyme synthesis and secretion as well as panc

173 d understanding of the mechanisms regulating digestive enzyme synthesis and secretion.

174 protein modulates pancreatic growth, but not digestive enzyme synthesis, via CCK-independent activati

175 n chitinase (AMCase) can function as a major digestive enzyme that constitutively degrades chitin sub

176 Pancreatic ribonuclease (RNASE1) is a digestive enzyme that has been one of the key models in

177 tive fluid, and found that pactacin is novel digestive enzyme that is specific in teleosts.

178 nse to lipid intake; it regulates pancreatic digestive enzymes that are required for absorption of nu

179 m hyperinsulinemia promoted the secretion of digestive enzymes that contributed to acinar to ductal m

180 the earliest protease molecules were simple digestive enzymes that gained complex regulatory functio

181 Acinar cells produce digestive enzymes that impede transcriptomic characteriz

182 ights on the binding preferences of malarial digestive enzymes that were used to design specific meth

183 s of the intestine are polarized and express digestive enzymes, the hepatocytes secrete bile, and the

184 and indirectly by impairing the activity of digestive enzymes, the latter event causing the accumula

185 a complex process consisting of intraluminal digestive enzymes, the unstirred mucus layer, and a syst

186 at pH 6.0, which reduced its degradation by digestive enzymes, thus increasing its bio-accessibility

187 The resulting easy accessibility of digestive enzymes to alpha-kafirin, the major storage pr

188 astroduodenal digestion alpha-DCs react with digestive enzymes to produce carbonylated proteins.

189 e starch and proteins limiting the access of digestive enzymes to their substrates.

190 h an animal gut (replete with its associated digestive enzymes) to disrupt the barrier and permit ger

191 pecies identified positive selection for the digestive enzyme trehalase in insect eaters, while sucra

192 The digestive enzyme trypsin is an important driver of pancr

193 Human cationic trypsinogen, precursor of the digestive enzyme trypsin, can be rapidly degraded to pro

194 Recombinant SLPI attenuates digestive enzyme (trypsin)- or leukocyte proteinase (ela

195 ol, repeatedly exposing proteoliposomes to a digestive enzyme, trypsin, was developed and compared wi

196 Premature intracellular activation of the digestive enzyme trypsinogen is considered to be the ini

197 On incubation of Ara h 1 with digestive enzymes, various protease-resistant fragments

198 ids chosen against the two classes of starch digestive enzymes was confirmed through various analytic

199 ile, antioxidant activity, and inhibition of digestive enzymes was evaluated in fruits of Butia catar

200 However, maturation of digestive enzymes was unaffected.

201 As non-interacting size mimics of digestive enzymes, we investigated the diffusion of fluo

202 ioxidant capacities and abilities to inhibit digestive enzymes were characterized.

203 the chosen food samples on lipid and starch digestive enzymes were determined by evaluating the lipa

204 f carotenoids with possible accessibility by digestive enzymes when consumed but this affects cooking

205 The exocrine pancreas is the main source of digestive enzymes which are released from secretory vesi

206 ra elevates the expression of genes encoding digestive enzymes while in the foregut symbiotic organs,

207 The exocrine compartment makes and secretes digestive enzymes, while the endocrine compartment, orga

208 ion characterised by premature activation of digestive enzymes within acinar cells, followed by necro

209 Continuous regeneration of digestive enzyme (zymogen)-secreting chief cells is a no

210 Intra-acinar cell activation of digestive enzyme zymogens including trypsinogen is gener

211 the premature intrapancreatic activation of digestive enzyme zymogens.