about
Transforming growth factor-β2 and endotoxin interact to regulate homeostasis via interleukin-8 levels in the immature intestine.Glucose transport by epithelia prepared from harvested enterocytes.Preterm Birth Reduces Nutrient Absorption With Limited Effect on Immune Gene Expression and Gut Colonization in Pigs.The usefulness of in vitro models to predict the bioavailability of iron and zinc: a consensus statement from the HarvestPlus expert consultation.Modulation of intestinal inflammation by minimal enteral nutrition with amniotic fluid in preterm pigs.Pasteurization Procedures for Donor Human Milk Affect Body Growth, Intestinal Structure, and Resistance against Bacterial Infections in Preterm Pigs.α1,2-Fucosyllactose Does Not Improve Intestinal Function or Prevent Escherichia coli F18 Diarrhea in Newborn Pigs.Glucagon-like peptide-2 induces rapid digestive adaptation following intestinal resection in preterm neonates.Effects of bovine lactoferrin on the immature porcine intestine.Postnatal amniotic fluid intake reduces gut inflammatory responses and necrotizing enterocolitis in preterm neonates.Parenteral lipids and partial enteral nutrition affect hepatic lipid composition but have limited short term effects on formula-induced necrotizing enterocolitis in preterm piglets.Aldohexose malabsorption in preterm pigs is directly related to the severity of necrotizing enterocolitis.Provision of Amniotic Fluid During Parenteral Nutrition Increases Weight Gain With Limited Effects on Gut Structure, Function, Immunity, and Microbiology in Newborn Preterm Pigs.Bioactive Whey Protein Concentrate and Lactose Stimulate Gut Function in Formula-fed Preterm Pigs.Human milk oligosaccharide effects on intestinal function and inflammation after preterm birth in pigs.Bovine colostrum improves neonatal growth, digestive function, and gut immunity relative to donor human milk and infant formula in preterm pigs.Processing of whey modulates proliferative and immune functions in intestinal epithelial cells.Minimal short-term effect of dietary 2'-fucosyllactose on bacterial colonisation, intestinal function and necrotising enterocolitis in preterm pigs.Casein addition to a whey-based formula has limited effects on gut function in preterm pigs1Prematurity does not markedly affect intestinal sensitivity to endotoxins and feeding in pigsTransition from parenteral to enteral nutrition induces immediate diet-dependent gut histological and immunological responses in preterm neonatesThe Incidence of Necrotizing Enterocolitis Is Increased Following Probiotic Administration to Preterm PigsHuman Milk Oligosaccharides to Prevent Gut Dysfunction and Necrotizing Enterocolitis in Preterm NeonatesBovine Milk Oligosaccharides with Sialyllactose for Preterm PigletsViable, lyophilized lactobacilli do not increase iron absorption from a lactic acid-fermented meal in healthy young women, and no iron absorption occurs in the distal intestineIncreased Intestinal Inflammation and Digestive Dysfunction in Preterm Pigs with Severe Necrotizing EnterocolitisAlpha-Lactalbumin Enriched Whey Protein Concentrate to Improve Gut, Immunity and Brain Development in Preterm PigsBovine Milk Oligosaccharides with Sialyllactose Improves Cognition in Preterm Pigs
P50
Q34664048-B0DCC06C-BF8A-45B6-80BB-5A209153CCA3Q34962146-0AD28BF0-7D8B-4AC4-B73D-9FFA368A5A6CQ35604886-8CC46092-8E78-48C1-8517-813CDD223419Q36482764-0B2B0E3E-8EDC-4D6E-B8D6-FB488635FE44Q39146443-334BF9F0-608C-406E-A27B-7BAA848806C5Q40292572-08B6F2A6-3C42-4495-9ED5-975ECD65B51AQ40652262-26A9497B-551F-4C26-BCDD-E86443FADF28Q41393541-C2F390B8-742F-4A31-A6DE-19BE73B51ADEQ43937010-9D2ED99F-70F5-49B7-A8D8-E04D594E5F66Q45231130-00C83156-89AB-4BF5-8614-90EDBEAF0244Q45863867-4B36C952-7539-4EFF-A4EF-A51922081E44Q46689940-2320B867-8919-4FB5-AF2F-48006E7B7C97Q47410454-93A2C718-C5A3-4018-BEAF-54110E47D47DQ48017300-0B2B3514-21C8-426E-ADB1-ABBE38437AE9Q51302154-F0466208-06A7-446A-B128-ABD77CA8117EQ52849556-E1A2165C-1165-4497-B685-4D2FDD74852FQ53229351-DFE4F95D-D2BC-423F-BC2A-8461ED8874E3Q53776466-84E0228A-44DE-4D0E-ABB1-2FE8FD716305Q56835369-0735881F-83CF-42FD-B9C7-86FD70BA2DD8Q56835377-EE3D37C1-09C7-48A2-BBD7-1F54C26CB1C5Q56835381-043396AC-CC8E-4565-AFA5-81A4A1E45C24Q56835387-166B1410-60B5-420C-978D-CA58D3CDBF31Q57295690-42141E37-B99C-40DA-91EE-29B40B4312ECQ57472108-BD93B21C-031C-40BE-9CC5-3A2266C21741Q59613955-199CA6AA-2CB0-4745-8377-7B0423A3CEE0Q60368019-8EC8742D-4E68-4351-BD27-DFA3BD1F92E4Q92812601-F570E812-9835-45B5-B3A5-AF5612AA9580Q92814662-519F7B80-95FD-4F35-A56A-822B337906F0
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Stine B Bering
@ast
Stine B Bering
@en
Stine B Bering
@es
Stine B Bering
@nl
type
label
Stine B Bering
@ast
Stine B Bering
@en
Stine B Bering
@es
Stine B Bering
@nl
prefLabel
Stine B Bering
@ast
Stine B Bering
@en
Stine B Bering
@es
Stine B Bering
@nl
P106
P1153
13204239900
P31
P496
0000-0002-6125-7892