• <em>RPS6KA3</em>-Related Intellectual Disability
• Accelerated tooth movement in Rsk2-deficient mice with impaired cementum formation
• Airway management of a patient with coffin-lowry syndrome: a case report
• An unexpected presentation of very severe hypertriglyceridemia in a boy with Coffin-Lowry syndrome: a case report
• Case Report: Chinese female patients with a heterozygous pathogenic <em>RPS6KA3</em> gene variant c.898C&gt;T and distal 22q11.2 microdeletion
• Chewing and swallowing training in Coffin-Lowry syndrome: A case report
• Coffin-Lowry Syndrome Induced by <em>RPS6KA3</em> Gene Variation in China: A Case Report in Twins
• Coffin-Lowry Syndrome Induced by RPS6KA3 Gene Variation in China: A Case Report in Twins
• Defective synaptic plasticity in a model of Coffin-Lowry syndrome is rescued by simultaneously targeting PKA and MAPK pathways
• Delayed postnatal brain development and ontogenesis of behavior and cognition in a mouse model of intellectual disability
• Establishment of linkage phase, using Oxford Nanopore Technologies, for preimplantation genetic testing of Coffin-Lowry syndrome with a <em>de novo RPS6KA3</em> mutation
• Establishment of linkage phase, using Oxford Nanopore Technologies, for preimplantation genetic testing of Coffin-Lowry syndrome with a de novo RPS6KA3 mutation
• Exploring the impacts of a coffin-lying experience on life and death attitudes of medical and nursing students: preliminary findings
• First female Korean child with Coffin-Lowry syndrome: a novel variant in RPS6KA3 diagnosed by exome sequencing and a literature review
• Identification of a New Mutation in <em>RSK2</em>, the Gene for Coffin-Lowry Syndrome (CLS), in Two Related Patients with Mild and Atypical Phenotypes
• Identification of a New Mutation in RSK2, the Gene for Coffin-Lowry Syndrome (CLS), in Two Related Patients with Mild and Atypical Phenotypes
• Identification of RSK substrates using an analog-sensitive kinase approach
• Mitral valve repair and tricuspid annuloplasty for Coffin-Lowry syndrome
• Modeling suggests combined-drug treatments for disorders impairing synaptic plasticity via shared signaling pathways
• Novel RPS6KA3 mutations cause Coffin-Lowry syndrome in two patients and concurrent compulsive eyebrow-pulling behavior in one of them
• Premature Loss of Deciduous Teeth as a Symptom of Systemic Disease: A Narrative Literature Review
• Quantitative description of the interactions among kinase cascades underlying long-term plasticity of Aplysia sensory neurons
• Short Bones, Renal Stones, and Diagnostic Moans: Hypercalcemia in a Girl Found to Have Coffin-Lowry Syndrome