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Publications by J. M. Devaney

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

English

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MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches

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Rett Syndrome Without MECP2 Mutation in a Pakistani Girl

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Refining the Phenotype of Common Mutations in Rett Syndrome

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

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

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Inhibition of Gsk3b Reduces Nfkb1 Signaling and Rescues Synaptic Activity to Improve the Rett Syndrome Phenotype in Mecp2 -Knockout Mice

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Suppressor Mutations in Mecp2-Null Mice Reveal That the DNA Damage Response Is Key to Rett Syndrome Pathology

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

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