Pages that link to "Q38711921"
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The following pages link to Identification and characterization of a missense mutation in the O-linked β-N-acetylglucosamine (O-GlcNAc) transferase gene that segregates with X-linked intellectual disability (Q38711921):
Displaying 20 items.
- Mutations in N-acetylglucosamine (O-GlcNAc) transferase in patients with X-linked intellectual disability (Q38742160) (← links)
- Nutrient-driven O-GlcNAc in proteostasis and neurodegeneration (Q47628534) (← links)
- The O-GlcNAc Transferase Intellectual Disability Mutation L254F Distorts the TPR Helix. (Q52722412) (← links)
- Thio-Linked UDP-Peptide Conjugates as O-GlcNAc Transferase Inhibitors. (Q55287157) (← links)
- O-GlcNAc cycling in the developing, adult and geriatric brain. (Q55416370) (← links)
- Proteomic analysis of the OGT interactome: novel links to epithelial-mesenchymal transition and metastasis of cervical cancer (Q57293808) (← links)
- -GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling (Q58060859) (← links)
- Critical observations that shaped our understanding of the function(s) of Intracellular Glycosylation (O-GlcNAc) (Q58564337) (← links)
- The Many Ways by Which -GlcNAcylation May Orchestrate the Diversity of Complex Glycosylations (Q58617479) (← links)
- Involvement of O-GlcNAcylation in the Skeletal Muscle Physiology and Physiopathology: Focus on Muscle Metabolism (Q59127958) (← links)
- Acutely elevated O-GlcNAcylation suppresses hippocampal activity by modulating both intrinsic and synaptic excitability factors (Q64057364) (← links)
- Nutrient regulation of signaling and transcription (Q64251360) (← links)
- Structural Perspective on Revealing and Altering Molecular Functions of Genetic Variants Linked with Diseases (Q64273189) (← links)
- Protein ensembles link genotype to phenotype. (Q64967550) (← links)
- O-GlcNAc in cancer: An Oncometabolism-fueled vicious cycle (Q88210290) (← links)
- An intellectual disability syndrome with single-nucleotide variants in O-GlcNAc transferase (Q89811375) (← links)
- O-GlcNAcase contributes to cognitive function in Drosophila (Q89865307) (← links)
- Molecular Interrogation to Crack the Case of O-GlcNAc (Q90616209) (← links)
- Catalytic deficiency of O-GlcNAc transferase leads to X-linked intellectual disability (Q91807315) (← links)
- A complex containing the O-GlcNAc transferase OGT-1 and the ubiquitin ligase EEL-1 regulates GABA neuron function (Q92282106) (← links)