Evidence map›Paper›PMID 19818631›Full record

ReviewTrends in biochemical sciences2009

Lafora disease: insights into neurodegeneration from plant metabolism.

Matthew S Gentry, Jack E Dixon, Carolyn A Worby

Abstract readReview
In one paragraph

Review in Trends in biochemical sciences, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 92 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Structural biology of glucan phosphatases from humans to plants.Current opinion in structural biology · 2016
    Review
  15. Review
  16. Review
  17. Incorporation of phosphate into glycogen by glycogen synthase.Archives of biochemistry and biophysics · 2016
    Article
  18. Review
  19. Glycogen phosphorylation and Lafora disease.Molecular aspects of medicine · 2015
    Review
  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

3 authors at 2 institutions in 1 country.

Matthew S GentryDepartment of Molecular and Cellular Biochemistry and Center for Structural Biology, University of Kentucky, Lexington, KY 40536-0509, USA. matthew.gentry@uky.edu
Jack E Dixon
Carolyn A Worby
University of California, San Diego · USUniversity of Kentucky · US

Funding

UNDERSTANDING THE MOLECULAR BASIS OF EPIGENETIC TRANSCRIPTIONAL SILENCINGP20RR020171 · NCRR · UNIVERSITY OF KENTUCKY · PI LOUIS HERSH, LOUIS HERSH LOUIS HERSH · 2004 to 2011
$16.5M
REGULATION OF NEUROPEPTIDE BIOSYNTHESISR01DK018849 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DIXON, JACK E, WORBY, CAROLYN ANN · 1986 to 2020
$7.0M
Novel Model Systems Link Floridean Starch Metabolism to Lafora DiseaseR00NS061803 · NINDS · UNIVERSITY OF KENTUCKY · PI GENTRY, MATTHEW S. · 2008 to 2010
$696k
Use of Novel Model Systems Link Floridean Starch Metabolism to Lafora DiseaseK99NS061803 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GENTRY, MATTHEW S. · 2007 to 2008
$154k
Howard Hughes Medical InstituteNCRR NIH HHS P20 RR020171NCRR NIH HHS RR0202171NIDDK NIH HHS DK0118849NIDDK NIH HHS R01 DK018849NINDS NIH HHS K99 NS061803NINDS NIH HHS NS061803NINDS NIH HHS R00 NS061803
6 · The paper itself

Abstract

Reversible phosphorylation modulates nearly every step of glycogenesis and glycogenolysis. Multiple metabolic disorders are the result of defective enzymes that control these phosphorylation events, enzymes that were identified biochemically before the advent of the molecular biology era. Lafora disease is a metabolic disorder resulting in accumulation of water-insoluble glucan in the cytoplasm, and manifests as a debilitating neurodegeneration that ends with the death of the patient. Unlike most metabolic disorders, the link between Lafora disease and metabolism has not been defined in almost 100 years. The results of recent studies with mammalian cells, mouse models, eukaryotic algae, and plants have begun to define the molecular mechanisms that cause Lafora disease. The emerging theme identifies a new phosphorylation substrate in glycogen metabolism, the glucan itself.

Indexed as

AnimalsCarrier ProteinsHumansLafora DiseaseModels, BiologicalNeurodegenerative DiseasesProtein Tyrosine Phosphatases, Non-ReceptorUbiquitin-Protein LigasesCarrier ProteinsEPM2A protein, humanNHLRC1 protein, humanProtein Tyrosine Phosphatases, Non-ReceptorUbiquitin-Protein Ligases

Identifiers

PMID19818631
PMCPMC2805077
OpenAlexW1978829102

What OpenQuestion holds

Textmetadata
LicenceTDM
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.