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ProteomicsIDA (Iminodiacetic Acid) Generated Mesoporous Nanopolymer - A Template to Relate Surface Area, Hydrophilicity and Glycopeptides Enrichment
Co-polymer 1,2-epoxy-5-hexene and divinyl benzene with terminal oxirane group is synthesized for the first time. High density of hydrophilic groups (-COOH, -OH) enhances hydrophilicity through facile functionalization with Diethylene Triamine (DETA) and chloroacetic acid. COOH-functionalized mesopor...
ORGANISM(S): Homo sapiens (Human) 
2023-07-20 | PXD027783 | Pride
Lc-ms/ms Spe Polymer Glycopeptides Enrichment 
ProteomicsBiallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia by impairing autophagy
Neurodevelopmental disorders have great clinical and genetic heterogeneity and are known to arise from dysfunction in components of diverse cellular pathways, the precise pathomechanism for the majority however remains elusive. We studied five patients from three unrelated families originating from ...
ORGANISM(S): Homo sapiens (Human) 
2024-10-17 | PXD044735 | Pride
Microcephaly Autophagy Zftraf1 
UnknownEnhanced nonlinear optical response of alkalides based on stacked Janus all-cis-1,2,3,4,5,6-hexafluorocyclohexane.
Not available
S-EPMC10474417 | biostudies-literature
UnknownIn silico elucidation of potential drug targets against oxygenase domain of Human eNOS Dysfunction.
Not available
S-EPMC10132633 | biostudies-literature
UnknownExperimental Validation of MHC Class I and II Peptide-Based Potential Vaccine Candidates for Human Papilloma Virus Using Sprague-Dawly Models.
Not available
S-EPMC9968051 | biostudies-literature
UnknownRole of single or double ringed circumferential wound protectors in reducing surgical site infections following colorectal resections. A systematic review.
Not available
S-EPMC9577642 | biostudies-literature
UnknownStructural and evolutionary constraints shape adaptive landscapes of immune-related genes across mammalian phylogeny.
Not available
S-EPMC12594431 | biostudies-literature
ProteomicsDe novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway
Main purpose of the project is to delineate the consequences of de novo variants identified in patients manifesting intellectual disability-craniodigital syndrome. To this end, we investigated the effects of mutated CK2β by performing phosphor proteome profiling of patient derived LCLs along with th...
ORGANISM(S): Homo sapiens (Human) 
2022-05-04 | PXD029983 | Pride
Csnk2b Ck2β and ck2 
ProteomicsDe novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway
Main purpose of the project is to delineate the consequences of de novo variants identified in patients manifesting intellectual disability-craniodigital syndrome. By employing pulldown assay coupled with mass spectrometry, we investigated the novel binding partners of CK2β and tried to find the imp...
ORGANISM(S): Homo sapiens (Human) 
2022-05-04 | PXD029970 | Pride
Csnk2b Ck2β and ck2 
UnknownResponse of root development and nutrient uptake of two chinese cultivars of hybrid rice to nitrogen and phosphorus fertilization in Sichuan Province, China.
Not available
S-EPMC8604849 | biostudies-literature
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