Results 221 to 230 of about 99,858 (332)

BIOCHEMICAL OBSERVATIONS ON E. COLI MUTANTS DEFECTIVE IN URIDINE DIPHOSPHOGLUCOSE [PDF]

, 1962
T. A. Sundararajan, Annette M. C. Rapin, H. M. Kalckar   +2 more
openalex   +1 more source

Cell type mapping of mild malformations of cortical development with oligodendroglial hyperplasia in epilepsy using single‐nucleus multiomics

Epilepsia, EarlyView.
Abstract Objective Mild malformations of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) are brain lesions associated with focal epilepsy and characterized by increased oligodendroglial density, heterotopic neurons, and hypomyelination in the white matter.
Isabella C. Galvão, Manuela Lemoine, Ludmyla Kandratavicius, Clarissa L. Yasuda, Marina K. M. Alvim, Enrico Ghizoni, Ingmar Blümcke, Fernando Cendes, Fabio Rogerio, Iscia Lopes‐Cendes, Diogo F. T. Veiga   +10 more
wiley   +1 more source

Status epilepticus in older adults: A critical review

Epilepsia, EarlyView.
Abstract Older adults (≥60 years of age) have the highest incidence of status epilepticus (SE) among adults and experience the highest morbidity and mortality. SE incidence increases with age in adulthood. A recent study from Austria estimated an incidence of 89.6/100 000 and 67.6/100 000 person‐years adjusted for age and sex in women and men aged >60 ...
Matthew R. Woodward, Michael J. Armahizer, Tina I. Wang, Neeraj Badjatia, Emily L. Johnson, Emily J. Gilmore   +5 more
wiley   +1 more source

Phosphorylation of nucleosides by P-N bond species generated from prebiotic reduced phosphorus sources. [PDF]

Commun Chem
Gull M, Cruz HA, Krishnamurthy R, Pasek MA.   +3 more
europepmc   +1 more source

Uridine Diphosphate Glucose Dehydrogenase

, 1968
Pradip Roy‐Burman, S. Roy-Burman, Donald W. Visser   +2 more
openalex   +1 more source

Pharmacogenomics of Human Uridine Diphospho‐Glucuronosyltransferases and Clinical Implications

Clinical pharmacology and therapy, 2014
Chantal Guillemette, Éric Lévesque, Michèle Rouleau   +2 more
semanticscholar   +1 more source

Metabolomic and proteomic stratification of equine osteoarthritis

Equine Veterinary Journal, EarlyView.
Abstract Background Equine osteoarthritis (OA) is predominantly diagnosed through clinical examination and radiography, leading to detection only after significant joint pathology. The pathogenesis of OA remains unclear and while many medications modify the disease's inflammatory components, no curative or reversal treatments exist.
James R. Anderson, Marie M. Phelan, Eva Caamaño‐Gutiérrez, Peter D. Clegg, Luis M. Rubio‐Martinez, Mandy J. Peffers   +5 more
wiley   +1 more source

Simply cut out - Combining CRISPR/Cas9 RNPs and transiently selected telomere vectors for marker free-gene deletion in <i>Trichoderma atroviride</i>. [PDF]

Front Genome Ed
Gründlinger M, Ellensohn C, Drechsel L, Schreiner U, Pierson S, Baldin C, Zeilinger S.   +6 more
europepmc   +1 more source

Pseudouridine: Still mysterious, but never a fake (uridine)!

RNA Biology, 2014
Felix Spenkuch, Y. Motorin, M. Helm
semanticscholar   +1 more source

In vivo modeling of lethal congenital contracture syndrome 1 suggests pathomechanisms in cellular stress responses

The FEBS Journal, EarlyView.
Gle1 knockout mice fail to segregate cell lineages at the blastocyst stage, resulting in very early embryonic lethality. Gle1 knock‐in (KI) mice harboring a pathogenic variant giving rise to lethal congenital contracture syndrome 1 show both known and novel innervation defects, supportive of multiorgan pathology in human fetuses.
Tomáš Zárybnický, Sonja Lindfors, Saana Metso, Julia Koivula, Zoltan Szabo, Rasmus Valtonen, Mikko Tulppo, Johanna Magga, Samu Saarimäki, Sonja Bläuer, Ilkka Miinalainen, Risto Kerkelä, Petteri. T. Piepponen, Vootele Voikar, Juho Väänänen, Riikka Kivelä, Bhagwan Yadav, Hanna Lindgren, Pirkko Mattila, Fu‐Ping Zhang, Petra Sipilä, Reetta Hinttala, Satu Kuure   +22 more
wiley   +1 more source