Associated Papers
The structure of the IL-11 signalling complex provides insight into receptor variants associated with craniosynostosis.
Sentosa DD et al.
The Febs Journal, 2025
Molecular characterization of the craniosynostosis-associated interleukin-11 receptor variants p.T306_S308dup and p.E364_V368del.
Kespohl B et al.
The Febs Journal, 2024
Craniosynostosis-associated variants in the IL-11R complex: new insights and questions.
Sims NA et al.
The Febs Journal, 2024
Mutations in Craniosynostosis Patients Cause Defective Interleukin-11 Receptor Maturation and Drive Craniosynostosis-like Disease in Mice.
Agthe M et al.
Cell Reports, 2018
IL11RA-related Crouzon-like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differences.
Brischoux-Boucher E et al.
Clinical Genetics, 2018
Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon-like craniosynostosis.
Keupp K et al.
Molecular Genetics & Genomic Medicine, 2013
Select a paper to view details