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Preclinical research in Rett syndrome: setting the foundation for translational success.Academic Article Why?
A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome.Academic Article Why?
Rett syndrome induced pluripotent stem cell-derived neurons reveal novel neurophysiological alterations.Academic Article Why?
Global transcriptional and translational repression in human-embryonic-stem-cell-derived Rett syndrome neurons.Academic Article Why?
MECP2 isoform-specific vectors with regulated expression for Rett syndrome gene therapy.Academic Article Why?
Safety, pharmacokinetics, and preliminary assessment of efficacy of mecasermin (recombinant human IGF-1) for the treatment of Rett syndrome.Academic Article Why?
A protocol for evaluation of Rett Syndrome symptom improvement by metabolic modulators in Mecp2-mutant mice.Academic Article Why?
Evaluation of Rett Syndrome Symptom Improvement by Metabolic Modulators in Mecp2-Mutant Mice.Academic Article Why?
Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation.Academic Article Why?
X-chromosome inactivation in rett syndrome human induced pluripotent stem cells.Academic Article Why?
A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome.Academic Article Why?
Paroxysmal alpha activity in Rett syndrome: a case report.Academic Article Why?
Lymphocyte function in autism and Rett syndrome.Academic Article Why?
Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.Academic Article Why?
Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature.Academic Article Why?
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