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ProteomicsRegulation of AMP synthesis by a KCTD13 ubiquitin ligase connects 16p11.2 deletion syndrome to a metabolic disorder with autistic features
Madison JM, Duong K, Vieux EF, Iqbal S, Requadt E, Udeshi ND, Fereshetian S, Lewis MC, Gomes AS, Pierce KA, Platt RJ, Zhang F, Campbell AJ, Lal D, Wagner FF, Clish CB, Carr SA, Scolnick EM, Cottrell JR. 2020. Genetic variation of KCTD13 at the 16p11.2 deletion locus and of CUL3 are linked with autis...
ORGANISM(S): Mus Musculus (ncbitaxon:10090) 
2020-07-29 | MSV000085846 | MassIVE
UnknownCell type-specific mechanism of Setd1a heterozygosity in schizophrenia pathogenesis.
Not available
S-EPMC8896793 | biostudies-literature
UnknownTwo non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia.
Not available
S-EPMC4117700 | biostudies-literature
UnknownCopy number variation in schizophrenia in Sweden.
Not available
S-EPMC4271733 | biostudies-literature
UnknownRegulation of purine metabolism connects KCTD13 to a metabolic disorder with autistic features.
Not available
S-EPMC7773955 | biostudies-literature
UnknownKinetically Selective Inhibitors of Histone Deacetylase 2 (HDAC2) as Cognition Enhancers.
Not available
S-EPMC4310013 | biostudies-literature
UnknownA polygenic burden of rare disruptive mutations in schizophrenia.
Not available
S-EPMC4136494 | biostudies-literature
UnknownDe novo mutations in schizophrenia implicate synaptic networks.
Not available
S-EPMC4237002 | biostudies-literature
UnknownExploiting an Asp-Glu "switch" in glycogen synthase kinase 3 to design paralog-selective inhibitors for use in acute myeloid leukemia.
Not available
S-EPMC6553635 | biostudies-literature
UnknownAn inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.
Not available
S-EPMC4030770 | biostudies-literature
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