Rett Syndrome Latest Advances

Mecp2 deficiency induces dysphagia in a preclinical model of Rett Syndrome.

Journal: bioRxiv : the preprint server for biology

Published: December 03, 2025

MeCP2 interacts with the super elongation complex to regulate transcription.

Journal: Science advances

Published: November 26, 2025

Ganaxolone, an approved therapy for CDKL5-Deficiency Disorder, is an inhibitor of PTP1B.

Journal: bioRxiv : the preprint server for biology

Published: November 24, 2025

Reciprocal regulation of the H 3 histamine receptor in Rett syndrome and MECP2 Duplication syndrome: implications for therapeutic development.

Journal: bioRxiv : the preprint server for biology

Published: November 24, 2025

Astrocyte SEMA3C reduction improves Rett Syndrome phenotypes.

Journal: bioRxiv : the preprint server for biology

Published: November 24, 2025

Epidemiology and Healthcare Resource Utilization of Rett Syndrome in Canada: the Ontario experience.

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

Published: November 21, 2025

Brain assembloids decode human cortical networks in Rett syndrome.

Journal: Cell reports

Published: November 11, 2025

Altered activity of mPFC pyramidal neurons and parvalbumin-expressing interneurons during social interactions in a Mecp2 mousemodel for Rett syndrome.

Journal: Journal of neurophysiology

Published: November 10, 2025

Risk of Ocular Pathology in Rett Syndrome.

Journal: Journal of pediatric ophthalmology and strabismus

Published: November 05, 2025

Communication and feeding skills in Rett syndrome: Case report.

Journal: Journal of intellectual & developmental disability

Published: October 15, 2025

Real-world benefits and tolerability of trofinetide for the treatment of Rett syndrome: The LOTUS study.

Journal: Developmental medicine and child neurology

Published: October 09, 2025

MeCP2 at the crossroads of hypoxia, oxidative stress, and gene regulation in Rett syndrome.

Journal: Epigenomics

Published: October 03, 2025

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Mecp2 deficiency induces dysphagia in a preclinical model of Rett Syndrome.

Mecp2 deficiency induces dysphagia in a preclinical model of Rett Syndrome.

MeCP2 interacts with the super elongation complex to regulate transcription.

MeCP2 interacts with the super elongation complex to regulate transcription.

Ganaxolone, an approved therapy for CDKL5-Deficiency Disorder, is an inhibitor of PTP1B.

Ganaxolone, an approved therapy for CDKL5-Deficiency Disorder, is an inhibitor of PTP1B.

Reciprocal regulation of the H 3 histamine receptor in Rett syndrome and MECP2 Duplication syndrome: implications for therapeutic development.

Reciprocal regulation of the H 3 histamine receptor in Rett syndrome and MECP2 Duplication syndrome: implications for therapeutic development.

Astrocyte SEMA3C reduction improves Rett Syndrome phenotypes.

Astrocyte SEMA3C reduction improves Rett Syndrome phenotypes.

Epidemiology and Healthcare Resource Utilization of Rett Syndrome in Canada: the Ontario experience.

Epidemiology and Healthcare Resource Utilization of Rett Syndrome in Canada: the Ontario experience.

Brain assembloids decode human cortical networks in Rett syndrome.

Brain assembloids decode human cortical networks in Rett syndrome.

Altered activity of mPFC pyramidal neurons and parvalbumin-expressing interneurons during social interactions in a Mecp2 mousemodel for Rett syndrome.

Altered activity of mPFC pyramidal neurons and parvalbumin-expressing interneurons during social interactions in a Mecp2 mousemodel for Rett syndrome.

Risk of Ocular Pathology in Rett Syndrome.

Risk of Ocular Pathology in Rett Syndrome.

Communication and feeding skills in Rett syndrome: Case report.

Communication and feeding skills in Rett syndrome: Case report.

Real-world benefits and tolerability of trofinetide for the treatment of Rett syndrome: The LOTUS study.

Real-world benefits and tolerability of trofinetide for the treatment of Rett syndrome: The LOTUS study.

MeCP2 at the crossroads of hypoxia, oxidative stress, and gene regulation in Rett syndrome.

MeCP2 at the crossroads of hypoxia, oxidative stress, and gene regulation in Rett syndrome.