Evidence map›Paper›PMID 12545250›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2003

Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

Damina Balmer, Jared Goldstine, Y Manjula Rao, Janine M LaSalle

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 120 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. The MeCP2E1/E2-BDNF-Frontiers in cell and developmental biology · 2020
    Article
  9. Review
  10. Review
  11. Article
  12. DNA Methylation and Adult Neurogenesis.Brain plasticity (Amsterdam, Netherlands) · 2017
    Review
  13. Review
  14. Genetic control of postnatal human brain growth.Current opinion in neurology · 2017
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Damina BalmerMedical Microbiology and Immunology, Rowe Program in Human Genetics, School of Medicine, University of California, One Shields Avenue, Davis, CA 95616, USA.
Jared Goldstine
Y Manjula Rao
Janine M LaSalle
University of California, Davis · USUniversity of California System · US

Funding

The Role of MeCP2 in Rett SyndromeR01HD041462 · NICHD · UNIVERSITY OF CALIFORNIA DAVIS · PI LASALLE, JANINE M · 2002 to 2011
$2.8M
LSC ANALYSIS OF CELL CYCLE REGULATED CHROMOSOME DYNAMICSR21CA078851 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI LASALLE, JANINE M · 1998 to 2000
$144k
BRAIN AND TISSUE BANK FOR DEVELOPMENTAL DISORDERSN01HD013138 · NICHD · UNIVERSITY OF MARYLAND BALTIMORE · PI ZIELKE, H. RONALD · 1991 to 1998
–
NCI NIH HHS 1R21 CA 78851-01NICHD NIH HHS 1R01HD/NS 41462-01A1NICHD NIH HHS N01 HD 13138
6 · The paper itself

Abstract

Rett syndrome is caused by mutations in MECP2 and characterized by arrested postnatal neurodevelopment. MECP2 is ubiquitously expressed, but its protein product, methyl-CpG-binding protein 2 (MeCP2), is highly expressed in a subpopulation of cells in the adult brain. Automated quantitation of MeCP2 expression on a human developmental tissue microarray was performed by laser scanning cytometry. A significant correlation between age and MeCP2 level, population heterogeneity, and percentage of MeCP2 high-expressing cells was specifically observed in cerebral but not renal samples. In contrast, an inverse correlation between use of the long 3' UTR of MECP2 and age was observed, suggesting that an acquired switch in polyadenylation is responsible for the elevated MeCP2. Acquired elevated MeCP2 expression in neurons beginning in infancy and progressing through childhood may explain the delayed onset and developmental arrest of Rett syndrome

Indexed as

Chromosomal Proteins, Non-HistoneAdolescentAdultBrainChildChild, PreschoolDNA-Binding ProteinsFemaleFetusHumansInfantMaleMethyl-CpG-Binding Protein 2NeuronsPolyadenylationRepressor ProteinsChromosomal Proteins, Non-HistoneDNA-Binding ProteinsMECP2 protein, humanMethyl-CpG-Binding Protein 2Repressor Proteins

Identifiers

PMID12545250
OpenAlexW2142772281

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.