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Publications by J. Innis

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

English

Unbalanced 5;16 Translocation in a Boy With Papillary Thyroid Carcinoma

American Journal of Medical Genetics

English

Related publications

MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches

Journal of Neonatal Biology

English

Rett Syndrome and MeCP2

NeuroMolecular Medicine

Molecular Neuroscience

Molecular Medicine

English

Rett Syndrome Without MECP2 Mutation in a Pakistani Girl

Life and Science

English

Refining the Phenotype of Common Mutations in Rett Syndrome

Journal of Medical Genetics

English

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

Journal of Human Genetics

English

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

Pediatric Neurology

Developmental Neuroscience

English

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

Molecular Biology

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

English

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

Frontiers in Cellular Neuroscience

Molecular Neuroscience

English