Associated Papers
Micro-scale control of oligodendrocyte morphology and myelination by the intellectual disability-linked protein acyltransferase ZDHHC9.
Jeong HK et al.
Elife, 2025
Regulation of RAS palmitoyltransferases by accessory proteins and palmitoylation.
Yang A et al.
Nature Structural & Molecular Biology, 2024
Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature.
Mir A et al.
Bmc Medical Genomics, 2023
ZDHHC9 X-linked intellectual disability: Clinical and molecular characterization.
Ramos AKS et al.
American Journal of Medical Genetics. Part A, 2023
GCP16 stabilizes the DHHC9 subfamily of protein acyltransferases through a conserved C-terminal cysteine motif.
Nguyen PL et al.
Frontiers in Physiology, 2023
The X-Linked Intellectual Disability Gene Zdhhc9 Is Essential for Dendrite Outgrowth and Inhibitory Synapse Formation.
Shimell JJ et al.
Cell Reports, 2019
Expanding the molecular basis and phenotypic spectrum of ZDHHC9-associated X-linked intellectual disability.
Schirwani S et al.
American Journal of Medical Genetics. Part A, 2018
The first patient with sporadic X-linked intellectual disability with de novo ZDHHC9 mutation identified by targeted next-generation sequencing.
Han JY et al.
European Journal of Medical Genetics, 2017
Mutations in the X-linked intellectual disability gene, zDHHC9, alter autopalmitoylation activity by distinct mechanisms.
Mitchell DA et al.
The Journal of Biological Chemistry, 2014
Expanding the clinical phenotype of patients with a ZDHHC9 mutation.
Masurel-Paulet A et al.
American Journal of Medical Genetics. Part A, 2014
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus.
Raymond FL et al.
American Journal of Human Genetics, 2007
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