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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 
UnknownDe novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway.
Not available
S-EPMC9092267 | biostudies-literature
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