Results 281 to 290 of about 406,798 (331)

Protein glycosylation

open access: yesCurrent Biology, 2019
J. Eichler
semanticscholar   +1 more source

Pyrrolo[2,1‐f][1,2,4]triazin‐4‐amine: Synthesis, C7‐Functionalization, and NH2‐Derivatization via Buchwald–Hartwig‐Type Coupling

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
An optimized synthetic route and regioselective C7/NH2‐functionalization protocols for pyrrolo[2,1‐f][1,2,4]triazine‐4‐amine are disclosed, significantly enhancing accessibility and structural diversification of this relevant N‐heterocycle. An optimized gram‐scale synthetic route to pyrrolo[2,1‐f][1,2,4]triazin‐4‐amine is reported, affording an overall
Vinícius Rodrigues Durães Pereira   +7 more
wiley   +1 more source

Production of recombinant IgA1 with defined mucin-type O-glycans in <i>Nicotiana tabacum</i> BY-2 cells. [PDF]

open access: yesFront Plant Sci
Bailly N   +4 more
europepmc   +1 more source

Influence of Levulinoyl Protecting Groups on Glycosylation Stereoselectivity and Glycosyl Cation Structure

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
The influence of levulinoyl protecting groups on the glycosylation stereoselectivity and glycosyl cation structure is studied for galactose and mannose building blocks. The stereoselective synthesis of 1,2‐cis glycosidic bonds is historically challenging, and a common synthetic approach is based on the participation of remote protecting ester groups ...
Niklas Geue   +8 more
wiley   +1 more source

An overview of protein <i>N</i>-glycosylation diversity in microalgae. [PDF]

open access: yesFront Plant Sci
van Bockstaele-Fuentes J   +6 more
europepmc   +1 more source

Seizures and electroencephalographic findings in inborn errors of metabolism: Clues to differential diagnosis in the neonatal period, infancy, childhood and adolescence, and review of the literature

open access: yesEpileptic Disorders, EarlyView.
Abstract Although inborn errors of metabolism (IEM) are a rare cause of epilepsy, seizures are a common presentation in these disorders. Seizures in IEM are frequently refractory to conventional anti‐seizure medication and might warrant initiation of specific treatments based on vitamins or dietary modifications or provision of alternative substrates ...
D. Kapoor   +7 more
wiley   +1 more source

Inherited metabolic epilepsies–established diseases, new approaches

open access: yesEpilepsia Open, EarlyView.
Abstract Inherited metabolic epilepsies (IMEs) represent the inherited metabolic disorders (IMDs) in which epilepsy is a prevailing component, often determining other neurodevelopmental outcomes associated with the disorder. The different metabolic pathways affected by individual IMEs are the basis of their rarity and heterogeneity.
Itay Tokatly Latzer, Phillip L. Pearl
wiley   +1 more source

Equal Prevalence of Genotypes ON1 and BA of Human Orthopneumovirus in Riyadh, Saudi Arabia, in 2022. [PDF]

open access: yesCurr Issues Mol Biol
Ahmed A   +5 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy