Results 91 to 100 of about 20,673 (207)

Metabolomic Insights Into the Impact of a Maternal Western‐Style Diet and Leptin Supplementation During Suckling on Adult Rat Offspring

The FASEB Journal, Volume 40, Issue 2, 31 January 2026.
Plasma metabolites in adult offspring reflecting metabolic programming during critical developmental windows. ABSTRACT Perinatal nutrition influences offspring metabolic phenotype and obesity risk. This study examines how a maternal obesogenic diet and offspring's leptin supplementation during suckling affect the metabolome in offspring adulthood ...
Catalina A. Pomar, Rocío A. Martin‐Chamorro, Petr Zouhar, Pedro Castillo, Tomas Cajka, Jan Kopecky, Andreu Palou, Mariona Palou, Catalina Picó   +8 more
wiley   +1 more source

Enzymatic formation of uridine diphosphate N‐acetyl‐D‐mannosaminuronic acid [PDF]

, 1974
Naoshi Ichihara, Nobutoshi Ishimoto, Eiji Ito   +2 more
openalex   +1 more source

The phospholipid-dependence of uridine diphosphate glucuronyltransferase. Reactivation of phospholipase A-inactivated enzyme by phospholipids and detergents [PDF]

, 1971
David Attwood, Allan B. Graham, G. C. Wood   +2 more
openalex   +1 more source

ENZYMATIC SYNTHESIS OF URIDINE DIPHOSPHATE XYLOSE AND URIDINE DIPHOSPHATE ARABINOSE [PDF]

Proceedings of the National Academy of Sciences, 1956
V, Ginsburg, E F, Neufeld, W Z, Hassid
openaire   +2 more sources

Cholestasis in Crigler–Najjar Syndrome Type I: An Uncommon Histopathological Finding in a Rare Disorder

Indian Journal of Medical Specialities
Crigler–Najjar syndrome is a rare autosomal recessive disorder characterized by severe unconjugated hyperbilirubinemia. Liver histopathology in Crigler–Najjar Syndrome typically reveals fibrosis, while features of cholestasis are rarely reported.
N. Namratha, Nisha Yadav, Manish Narang, Sumaira Khalil   +3 more
doaj   +1 more source

Properties of Dietary Flavone Glycosides, Aglycones, and Metabolites on the Catalysis of Human Endoplasmic Reticulum Uridine Diphosphate Glucuronosyltransferase 2B7 (UGT2B7). [PDF]

Nutrients, 2023
Xu T, Lv Y, Cui Y, Liu D, Xu T, Lu B, Yang X.   +6 more
europepmc   +1 more source

Perioperative Anaesthetic Management of a Patient of Gilbert’s Syndrome with Adult Congenital Heart Disease - A Rare Presentation

The Indian Anaesthetists' Forum, 2014
Gilbert's syndrome is a hereditary condition with the genetic mutation of the enzyme uridine diphosphate glucuronosyltransferase, characterized by intermittent jaundice in the absence of hemolysis or underlying liver disease.
Sambhunath Das, Neelam Agarwal
doaj  

Biosynthesis of uridine diphosphate N-Acetylglucosamine: An underexploited pathway in the search for novel antibiotics? [PDF]

IUBMB Life, 2022
Wyllie JA, McKay MV, Barrow AS, Soares da Costa TP.   +3 more
europepmc   +1 more source

Comparison of uridine diphosphate glucuronyltransferase activities synthesizing S- and O-β-D-glucuronides [PDF]

, 1972
H. Paul A. Illing, Geoffrey J. Dutton
openalex   +1 more source

Glucokinase Variant Proteins Are Resistant to Fasting-Induced Uridine Diphosphate Glucose-Dependent Degradation in Maturity-Onset Diabetes of the Young Type 2 Patients. [PDF]

Int J Mol Sci, 2023
Cho J, Horikawa Y, Oiwa Y, Hosomichi K, Yabe D, Imai T.   +5 more
europepmc   +1 more source