[HTML][HTML] Mutations in the transcriptional regulator MeCP2 severely impact key cellular and molecular signatures of human astrocytes during maturation
J Sun, S Osenberg, A Irwin, LH Ma, N Lee, Y Xiang… - Cell reports, 2023 - cell.com
Mutations in the MECP2 gene underlie a spectrum of neurodevelopmental disorders, most
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
Mutations in the transcriptional regulator MeCP2 severely impact key cellular and molecular signatures of human astrocytes during maturation
J Sun, S Osenberg, A Irwin, LH Ma, N Lee… - Cell …, 2023 - pubmed.ncbi.nlm.nih.gov
Mutations in the MECP2 gene underlie a spectrum of neurodevelopmental disorders, most
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
[HTML][HTML] Mutations in the transcriptional regulator MeCP2 severely impact key cellular and molecular signatures of human astrocytes during maturation
J Sun, S Osenberg, A Irwin, LH Ma, N Lee, Y Xiang… - Cell Reports, 2023 - Elsevier
Mutations in the MECP2 gene underlie a spectrum of neurodevelopmental disorders, most
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
[HTML][HTML] Mutations in the transcriptional regulator MeCP2 severely impact key cellular and molecular signatures of human astrocytes during maturation
J Sun, S Osenberg, A Irwin, LH Ma, N Lee, Y Xiang… - Cell Reports, 2023 - cell.com
Mutations in the MECP2 gene underlie a spectrum of neurodevelopmental disorders, most
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
Mutations in the transcriptional regulator MeCP2 severely impact key cellular and molecular signatures of human astrocytes during maturation.
J Sun, S Osenberg, A Irwin, LH Ma, N Lee, Y Xiang… - Cell Reports, 2023 - europepmc.org
Mutations in the MECP2 gene underlie a spectrum of neurodevelopmental disorders, most
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
Mutations in the transcriptional regulator MeCP2 severely impact key cellular and molecular signatures of human astrocytes during maturation
J Sun, S Osenberg, A Irwin, LH Ma, N Lee, Y Xiang… - 2023 - agris.fao.org
Mutations in the MECP2 gene underlie a spectrum of neurodevelopmental disorders, most
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
[HTML][HTML] Mutations in the transcriptional regulator MeCP2 severely impact key cellular and molecular signatures of human astrocytes during maturation
J Sun, S Osenberg, A Irwin, LH Ma, N Lee, Y Xiang… - Cell reports, 2023 - ncbi.nlm.nih.gov
Mutations in the MECP2 gene underlie a spectrum of neurodevelopmental disorders, most
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
Mutations in the transcriptional regulator MeCP2 severely impact key cellular and molecular signatures of human astrocytes during maturation.
J Sun, S Osenberg, A Irwin, LH Ma, N Lee, Y Xiang… - Cell Reports, 2023 - europepmc.org
Mutations in the MECP2 gene underlie a spectrum of neurodevelopmental disorders, most
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …
commonly Rett syndrome (RTT). We ask whether MECP2 mutations interfere with human …