Sort   by:  
 Page size 
ProteomicsPurification of Cross-linked RNA-Protein Complexes by Phenol-Toluol Extraction
Recent methodological advances allowed the identification of an increasing number of RNAbinding proteins (RBPs) and their RNA-binding sites. RNA interactome capture is, however, limited to proteins interacting with polyadenylated RNAs while RBPs associating with nonadenylate RNA classes cannot be pu...
ORGANISM(S): Homo sapiens (Human) Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344 
2019-03-12 | PXD009571 | Pride
Human Lc-msms Shotgun Salmonella Rna-binding proteins Ptex 
ProteomicsProtein synthesis in the developing neocortex at near-atomic resolution reveals Ebp1-mediated neuronal proteostasis at the 60S tunnel exit
Proteostasis must be finely tuned in the nervous system, as it represents an essential feature of neurodevelopment, and dominant pathology in neurodegenerative disease. At the gateway of proteostasis is the ribosome; however, the architecture of ribosomal complexes in the developing mammalian brain ...
ORGANISM(S): Mus musculus (Mouse) 
2021-01-04 | PXD014740 | Pride
Development Neocortex Ribosome Ebp1 Proteostasis Orbitrap 
ProteomicsProtein synthesis in the developing neocortex at near-atomic resolution reveals Ebp1-mediated neuronal proteostasis at the 60S tunnel exit
Proteostasis must be finely tuned in the nervous system, as it represents an essential feature of neurodevelopment, and dominant pathology in neurodegenerative disease. At the gateway of proteostasis is the ribosome; however, the architecture of ribosomal complexes in the developing mammalian brain ...
ORGANISM(S): Mus musculus (Mouse) 
2021-01-04 | PXD014841 | Pride
Development Neocortex Ribosome Ebp1 Proteostasis 
ProteomicsExpanding the phenotype of NUP85 mutations beyond nephrotic syndrome to Primary autosomal recessive microcephaly and Seckel syndrome spectrum disoders
Primary autosomal recessive microcepahly and Seckel syndrome spectrum disodrers (MCPH-SCKS) include a heterogenous group of autosomal recessive inherited diseases characterized by primary (congenital) microcephaly, the absence of visceral abnormalities and a variable degree of cognitive impairment, ...
ORGANISM(S): Homo sapiens (Human) 
2022-08-11 | PXD018838 | Pride
Human Lc-msms Nup85 Primary fibroblasts 
Unknown2,2,6-Trimethyl-5-[2-(4-methyl-phen-yl)ethyn-yl]-4H-1,3-dioxin-4-one.
Not available
S-EPMC2971386 | biostudies-literature
UnknownHydroxychloroquine versus placebo in the treatment of non-hospitalised patients with COVID-19 (COPE - Coalition V): A double-blind, multicentre, randomised, controlled trial.
Not available
S-EPMC8968238 | biostudies-literature
UnknownSoil erosion modelling: A global review and statistical analysis.
Not available
S-EPMC8140410 | biostudies-literature
UnknownPartial asynchrony of coniferous forest carbon sources and sinks at the intra-annual time scale.
Not available
S-EPMC11300610 | biostudies-literature
UnknownTreatment of Multisystem Inflammatory Syndrome in Children.
Not available
S-EPMC8220965 | biostudies-literature
UnknownTwo Phase 3 Trials of Gantenerumab in Early Alzheimer's Disease.
Not available
S-EPMC10794000 | biostudies-literature
Sort   by:  
 Page size