ライフサイエンスコーパス: isomaltase

1 its of both maltase-glucoamylase and sucrase-isomaltase.

2 changes in alkaline phosphatase and sucrase isomaltase.

3 me B (-74%; 95% CI: -82%, -62%), and sucrase isomaltase (-58%; 95% CI: -75%, -29%) in EED biopsies co

4 mylase, pancreatic alpha-amylase and sucrase-isomaltase (-8.2, -7.5, -7.7 and -7.5 kcal/mol; and -7.8

5 -96%), GLUT5 (28-89%) and the enzyme sucrase-isomaltase (82-97%) was observed.

6 only white tea extract inhibited sucrase and isomaltase activity and the inhibition was limited.

7 Induction of ITF and sucrase-isomaltase after MEK inhibition in HT29-N2 cells did not

8 idases, alpha-glucosidase, beta-glucosidase, isomaltase, alpha-mannosidase, and glucoamylase, were ob

9 ein showed strong homology to rabbit sucrase-isomaltase, an abundant intestinal enzyme.

10 essing high levels of Cdx2 expressed sucrase-isomaltase, an enterocyte-specific gene which is a well-

11 Both sucrase isomaltase and alkaline phosphatase (a GPI-anchored prot

12 ional brush-border enzymes (lactase, sucrase-isomaltase and dipeptidyl peptidase 4) and visible subep

13 ion factors regulating expression of sucrase-isomaltase and fatty acid-binding protein.

14 Inhibition of maltase, sucrase, isomaltase and glucoamylase activity by acarbose, epigal

15 Sucrase-isomaltase and lactase-phlorizin hydrolase expressions c

16 ionship of these nuclear proteins to sucrase-isomaltase and lactase-phlorizin hydrolase gene expressi

17 ne shows heterogeneous expression of sucrase-isomaltase and most lectin receptors.

18 and also a strong inhibitor of glucoamylase, isomaltase, and alpha-glucosidase.

19 erminal differentiation markers ITF, sucrase-isomaltase, and the mucin gene MUC2.

20 atalytic sites identical to those of sucrase-isomaltase, but the proteins are only 59% homologous.

21 40% (11%), SLFN12 by 61% (14%), and sucrase-isomaltase by 28% (8%) (n = 6, P < .05 for all).

22 ing sites were present in intestinal sucrase isomaltase, cdx-2 homeodomain protein, and intestinal fa

23 These results suggest that sucrase-isomaltase constitutes a promising drug target for impro

24 ate malabsorption was discovered: in sucrase-isomaltase deficiency, the enzyme fails to anchor in the

25 ic populations and causes congenital sucrase-isomaltase deficiency, which is an inability to break do

26 o describe the health of adults with sucrase-isomaltase deficiency.

27 SIF1-binding proteins may regulate sucrase-isomaltase expression during postnatal development, but

28 The sucrose isomaltase gene (SI), is expressed exclusively in the in

29 e SIF1 cis-regulatory element of the sucrase-isomaltase gene and to the CE-LPH1 cis-regulatory elemen

30 The sucrase-isomaltase gene promoter has multiple regulatory element

31 with a protein-binding motif in the sucrase-isomaltase gene promoter, competition assays, and antibo

32 ytic differentiation markers villin, sucrase-isomaltase, glucose transporter 2 (GLUT2), and dipeptidy

33 he heterologously expressed protein, sucrase-isomaltase is a cAMP-dependent epithelial chloride chann

34 A sucrase-isomaltase knockout (Sis-KO) mouse model was used to fur

35 as found in suckling animals without sucrase-isomaltase messenger RNA (mRNA), and a higher-molecular-

36 inhibits beta-glucosidase, glucoamylase, and isomaltase more strongly than 1-deoxynojirimycin where t

37 in older animals with expression of sucrase-isomaltase mRNA.

38 drolases dipeptidyl-peptidase IV and sucrase-isomaltase or with binding of 10 of the 12 lectins teste

39 ver, crystallographic structural analysis of isomaltase predicts that another aspartic acid residue f

40 and inhibits transactivation of the sucrase-isomaltase promoter by Cdx-2.

41 A critical factor in regulating the sucrase-isomaltase promoter is Cdx2, an intestine-specific homeo

42 proteins are subunits of the rabbit sucrase-isomaltase protein (SI) complex.

43 me trehalase in insect eaters, while sucrase-isomaltase showed selection in lineages with omnivorous

44 Brush-border sucrase-isomaltase (SI) activity is complementary, through diges

45 cell differentiation, expression of sucrase isomaltase (SI) and dipeptidyl-peptidase IV (DPP-IV), tw

46 moyl-phosphate synthase 1 (CPS1) and sucrase-isomaltase (SI) as signature proteins.

47 The sucrase-isomaltase (SI) c.273_274delAG loss-of-function variant

48 The mouse sucrase-isomaltase (SI) gene is an enterocyte-specific gene expr

49 The sucrase-isomaltase (SI) gene, which encodes an enterocyte brush

50 B), maltase-glucoamylase (MGAM), and sucrase-isomaltase (SI) genes on starch digestibility and glycem

51 -dependent integral membrane protein sucrase-isomaltase (SI) in the Caco2 intestinal epithelial cell

52 Sucrase-isomaltase (SI) is an intestinal membrane-associated alp

53 Sucrase isomaltase (SI), a transmembrane disaccharidase found in

54 Sucrase-isomaltase (SI), an intestine-specific gene, is induced

55 Sucrase-isomaltase (SI), lactase-phlorizin hydrolase (LPH), and

56 Sucrase-isomaltase (SI), the product of an enterocyte-specific g

57 ses, maltase-glucoamylase (MGAM) and sucrase-isomaltase (SI).

58 ids showed 100% homology with rabbit sucrase-isomaltase (SI).

59 proteins 1, 2, 3, 4, 5, 13, and 14; sucrase isomaltase (SI); dipeptidyl peptidase 4 (Dpp4); glucose

60 The brush border enzymes DPPIV and sucrase-isomaltase still correctly localize at the apical plasma

61 homologous functional subunits (sucrase and isomaltase) that both belong to the glycoside hydrolase

62 sialoglycoprotein receptor subunits, sucrase-isomaltase, the erythropoietin receptor, and two of the

63 analysis of the in vitro-translated sucrase-isomaltase was indistinguishable from that of the protei

64 A transmembrane apical protein, sucrase isomaltase, was found mispolarized in a subpopulation of