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Publications by Daniel C. Tarquinio

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

Pediatric Neurology

Developmental Neuroscience

English

Pubertal Development in Rett Syndrome Deviates From Typical Females

Pediatric Neurology

Developmental Neuroscience

English

Related publications

Rett Syndrome and MeCP2

NeuroMolecular Medicine

Molecular Neuroscience

Molecular Medicine

English

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

English

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

Frontiers in Cellular Neuroscience

Molecular Neuroscience

English

Rett Syndrome Without MECP2 Mutation in a Pakistani Girl

Life and Science

English

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

English

MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches

Journal of Neonatal Biology

English

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

Journal of Human Genetics

English

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

Journal of Musculoskeletal Disorders and Treatment

English

MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients

Frontiers in Genetics

Molecular Medicine

English