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Publications by Gabi Gerlitz

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

Frontiers in Cellular Neuroscience
Molecular NeuroscienceCellular
2019English

Related publications

Rett Syndrome and MeCP2

NeuroMolecular Medicine
Molecular NeuroscienceNeurologyMolecular MedicineCellular
2014English

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

Pediatric Neurology
Child HealthDevelopmental NeurosciencePediatricsPerinatologyNeurology
2015English

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

Neurology
Neurology
2001English

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

MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches

Journal of Neonatal Biology
2016English

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

Frontiers in Integrative Neuroscience
Molecular NeuroscienceSensory SystemsCellularCognitive Neuroscience
2019English

Lissencephaly Due to LIS1 Mutation

2020English

Bisphosphonates and MeCP2 Deficiency: Cellular Studies and Clinical Application in Rett Syndrome

Journal of Musculoskeletal Disorders and Treatment
2018English

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

Journal of Human Genetics
Genetics
2000English

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