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Methyl-CpG-Binding Protein 2

Known as: MeCP2, Methyl CpG Binding Protein 2, MeCP2 Protein 
Methyl-CpG-binding protein 2 (486 aa, ~52 kDa) is encoded by the human MECP2 gene. This protein plays a role in the repression of transcription… Expand
National Institutes of Health

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Highly Cited
2016
Highly Cited
2016
The postnatal neurodevelopmental disorder Rett syndrome, caused by mutations in MECP2, produces a diverse array of symptoms… Expand
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Highly Cited
2014
Highly Cited
2014
Mesenchymal stem cells (MSCs) have potential application for the treatment of ischemic heart diseases. Besides differentiation… Expand
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Highly Cited
2010
Highly Cited
2010
The X-linked transcriptional repressor methyl CpG binding protein 2 (MeCP2), known for its role in the neurodevelopmental… Expand
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Highly Cited
2008
Highly Cited
2008
Introduction: Osteoporosis is characterized by low BMD. Studies have shown that B cells may participate in osteoclastogenesis… Expand
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Highly Cited
2006
Highly Cited
2006
Loss-of-function mutations or abnormal expression of the X-linked gene encoding methyl CpG binding protein 2 (MeCP2) cause a… Expand
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Highly Cited
2006
Highly Cited
2006
Mutations in MECP2, encoding methyl CpG binding protein 2 (MeCP2), cause most cases of Rett syndrome (RTT), an X-linked… Expand
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Highly Cited
2004
Highly Cited
2004
MeCP2 is a methyl-CpG binding protein that can repress transcription of nearby genes. In humans, mutations in the MECP2 gene are… Expand
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Highly Cited
2000
Highly Cited
2000
Editor—Rett syndrome (RTT, MIM 312760) is a neurodevelopmental disorder characterised by normal early psychomotor development… Expand
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Highly Cited
1998
Highly Cited
1998
  • S. Kudo
  • Molecular and Cellular Biology
  • 1998
  • Corpus ID: 23450163
ABSTRACT Human leukosialin (CD43) is expressed in a cell lineage-specific as well as a differentiation stage-specific fashion… Expand
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Highly Cited
1997
Highly Cited
1997
MeCP2 is an abundant mammalian protein that binds to methylated CpG. We have found that native and recombinant MeCP2 repress… Expand
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