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UnknownNovel variants in <i>ZNF462</i> and phenotype update in patients with Weiss-Kruszka syndrome: a case series.
Not available
S-EPMC12433108 | biostudies-literature
UnknownFurther characterization of the 9q31 microdeletion phenotype; delineation of a common region of overlap containing ZNF462.
Not available
S-EPMC10009906 | biostudies-literature
UnknownZFP462 safeguards neural lineage specification by targeting G9A/GLP-mediated heterochromatin to silence enhancers.
Not available
S-EPMC10038669 | biostudies-literature
ProteomicsZFP462 safeguards neural lineage specification by targeting G9A/GLP-mediated heterochromatin to silence enhancers
ZNF462 haploinsufficiency is linked to Weiss-Kruszka Syndrome, a genetic disorder characterized by neurodevelopmental defects including Autism. Though conserved in vertebrates and essential for embryonic development the molecular functions of ZNF462 remain unclear. We identified its murine homolog Z...
ORGANISM(S): Mus musculus (Mouse) 
2023-05-10 | PXD037238 | Pride
Stem cells Lineage specification and heterochromatin Transcription factors Zfp462 
UnknownA thermodynamic analysis of CLC transporter dimerization in lipid bilayers.
Not available
S-EPMC10576108 | biostudies-literature
UnknownPlant dicistronic tRNA-snoRNA genes: a new mode of expression of the small nucleolar RNAs processed by RNase Z.
Not available
S-EPMC140725 | biostudies-literature
ProteomicsRevealing the transitory and local effect of the demethylation agent zebularine on plant development and proteome dynamics of Salix purpurea
DNA methylation plays major roles in the epigenetic regulation of gene expression, transposon and transcriptional silencing, and DNA repair, with implications in developmental processes and phenotypic plasticity. Relevantly for arboreal species, DNA methylation constitute a regulative layer in cell ...
ORGANISM(S): Sarracenia purpurea subsp. purpurea 
2024-01-08 | PXD045653 | Pride
Proteomics Cell wall Cytidine analogue Dna methylation Purple willow 
UnknownStructural basis of pH-dependent activation in a CLC transporter.
Not available
S-EPMC11262703 | biostudies-literature
UnknownHuman germline hedgehog pathway mutations predispose to fatty liver.
Not available
S-EPMC5613974 | biostudies-literature
UnknownLimb body wall complex, amniotic band sequence, or new syndrome caused by mutation in IQ Motif containing K (IQCK)?
Not available
S-EPMC4585450 | biostudies-literature
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