Maria H. Chahrour

Genetics · 2007–2014

A researcher in the Science corpus: 4 papers; trusts 7 researchers and is trusted by 1 researcher here, as inferred from the citation graph.

Subfields

Whom Maria H. Chahrour trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

  1. T. Bale
  2. W. Vale
  3. J. Gan
  4. A. Bird
  5. R. Jaenisch
  6. M. Holmes

Who trusts Maria H. Chahrour overall

  1. Akira Yoshii
  2. O. Marín
  3. H. Zoghbi
  4. A. Kazantsev
  5. M. Constantine‐Paton
  6. M. O’Connell
  7. Mark F. Bear

Papers from Maria H. Chahrour's perspective

Ordered by how strongly the researchers Maria H. Chahrour trusts endorse each paper. Same corpus, a different order for every researcher.

  1. DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation (Science)
  2. CRF and CRF receptors: role in stress responsivity and other behaviors. (Annual Review of Pharmacology and Toxicology)
  3. Reversal of Neurological Defects in a Mouse Model of Rett Syndrome (Science)
  4. Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males. (American Journal of Human Genetics)
  5. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome (Nature Genetics)
  6. Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. (Human Molecular Genetics)
  7. Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2 (Science)
  8. Postnatal Neurodevelopmental Disorders: Meeting at the Synapse? (Science)
  9. Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. (Neuron)
  10. The Methyl-CpG-binding Protein MeCP2 Links DNA Methylation to Histone Methylation* (Journal of Biological Chemistry)

Their papers