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Publications by Ceitidh Taylor

Structure of the MeCP2–TBLR1 Complex Reveals a Molecular Basis for Rett Syndrome and Related Disorders

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2017English

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The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders

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Child HealthDevelopmental NeurosciencePediatricsPerinatologyNeurology
2015English

Rett Syndrome and MeCP2

NeuroMolecular Medicine
Molecular NeuroscienceNeurologyMolecular MedicineCellular
2014English

MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches

Journal of Neonatal Biology
2016English

Interplay of LIS1 and MeCP2: Interactions and Implications With the Neurodevelopmental Disorders Lissencephaly and Rett Syndrome

Frontiers in Cellular Neuroscience
Molecular NeuroscienceCellular
2019English

Rett Syndrome Without MECP2 Mutation in a Pakistani Girl

Life and Science
2020English

MeCP2 Mutations in Children With and Without the Phenotype of Rett Syndrome

Neurology
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2001English

Molecular Systems Biology of Neurodevelopmental Disorders, Rett Syndrome as an Archetype

Frontiers in Integrative Neuroscience
Molecular NeuroscienceSensory SystemsCellularCognitive Neuroscience
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The Structure of Human GALNS Reveals the Molecular Basis for Mucopolysaccharidosis IV A

Journal of Molecular Biology
Structural BiologyMolecular BiologyBiophysics
2012English

Mutational Analysis of the MECP2 Gene in Japanese Patients With Rett Syndrome

Journal of Human Genetics
Genetics
2000English

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