Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome

BS Johnson, YT Zhao, M Fasolino, JM Lamonica… - Nature medicine, 2017 - nature.com
Mutations in MECP2 cause Rett syndrome (RTT), an X-linked neurological disorder
characterized by regressive loss of neurodevelopmental milestones and acquired …
被引用次数：117 相关文章
[PDF] vahedilab.com

[PDF][PDF] Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome

BS Johnson, YT Zhao, M Fasolino, JM Lamonica… - NATURE …, 2017 - vahedilab.com
RESULTS A system to genetically biotinylate MeCP2 in vivo Biotin-mediated affinity tagging
has been widely used in cell and animal models for multiple experimental approaches …

Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome.

BS Johnson, YT Zhao, M Fasolino, JM Lamonica… - Nature …, 2017 - europepmc.org
Mutations in MECP2 cause Rett syndrome (RTT), an X-linked neurological disorder
characterized by regressive loss of neurodevelopmental milestones and acquired …

Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome

BS Johnson, YT Zhao, M Fasolino, JM Lamonica… - Nature …, 2017 - pure.york.ac.uk
Mutations in MECP2 cause Rett syndrome (RTT), an X-linked neurological disorder
characterized by regressive loss of neurodevelopmental milestones and acquired …
[HTML] nih.gov

[HTML][HTML] Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome

BS Johnson, YT Zhao, M Fasolino, JM Lamonica… - Nature …, 2017 - ncbi.nlm.nih.gov
Mutations in MECP2 cause Rett syndrome (RTT), an X-linked neurological disorder
characterized by regressive loss of neurodevelopmental milestones and acquired …

Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome

BS Johnson, YT Zhao, M Fasolino… - Nature …, 2017 - utsouthwestern.elsevierpure.com
Mutations in MECP2 cause Rett syndrome (RTT), an X-linked neurological disorder
characterized by regressive loss of neurodevelopmental milestones and acquired …

Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome

BS Johnson, YT Zhao, M Fasolino… - Nature …, 2017 - pubmed.ncbi.nlm.nih.gov
Mutations in MECP2 cause Rett syndrome (RTT), an X-linked neurological disorder
characterized by regressive loss of neurodevelopmental milestones and acquired …
[PDF] researchgate.net

[PDF][PDF] Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome

BS Johnson, YT Zhao, M Fasolino, JM Lamonica… - Nat Med, 2017 - researchgate.net
Mutations in MECP2 cause Rett syndrome (RTT), an X-linked neurological disorder
characterized by regressive loss of neurodevelopmental milestones and acquired …

[引用][C] Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome

BS Johnson, YT Zhao, M Fasolino, JM Lamonica… - Nature Medicine, 2017 - cir.nii.ac.jp

Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome

BS Johnson, YT Zhao, M Fasolino, JM Lamonica… - Nature Medicine, 2017 - go.gale.com
Mutations in MECP2 cause Rett syndrome (RTT), an X-linked neurological disorder
characterized by regressive loss of neurodevelopmental milestones and acquired …