Evidence map›Paper›PMID 18834937›Full record

ReviewBiochimica et biophysica acta2009

Intrabody and Parkinson's disease.

Chun Zhou, Serge Przedborski

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. A Specific Mini-Intrabody Mediates Lysosome Degradation of Mutant Huntingtin.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Intrabodies as neuroprotective therapeutics.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2013
    Review
  10. Article
  11. Article
  12. Review
  13. Parkinson's disease.Sub-cellular biochemistry · 2012
    Review
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

2 authors.

Chun ZhouDepartment of Neurology, Columbia University, New York, NY 10032, USA.
Serge Przedborski

Funding

TRANSLATIONAL APPROACHES TO NEUROPROTECTION OF AXONS IN PDrP50NS038370 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BURKE, ROBERT E · 1999 to 2014
$24.0M
REGULATION OF TENSIONP01NS011766 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI HIRANO, MICHIO · 1985 to 2007
$9.1M
Proinflammatory enzymes in amytrophic lateral sclerosisR01NS042269 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PRZEDBORSKI, SERGE E · 2001 to 2012
$3.0M
Mechanisms of Bax-mediated cell death in the MPTP modelR01AG021617 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PRZEDBORSKI, SERGE E · 2003 to 2007
$1.6M
A novel cell-based high-throughput assay for ALSR21NS064191 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PRZEDBORSKI, SERGE E · 2009 to 2010
$384k
Early motor neuron alteration in a non-cell autonomous ALS modelR21NS062180 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PRZEDBORSKI, SERGE E · 2008 to 2009
$374k
CLINICAL RESEARCH CENTER FOR NEUROMUSCULAR DISEASEP50NS011766 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ROWLAND, LEWIS P · 1995 to 1995
–
NIA NIH HHS AG21617-01A1NIA NIH HHS R01 AG021617NINDS NIH HHS NS062180NINDS NIH HHS NS11766-27A1NINDS NIH HHS NS38370-09NINDS NIH HHS P01 NS011766NINDS NIH HHS P50 NS038370NINDS NIH HHS R01 NS042269NINDS NIH HHS R21 NS062180NINDS NIH HHS R21 NS064191
6 · The paper itself

Abstract

The intrabody technology has become a promising therapeutic avenue for a variety of incurable diseases. This technology is an intracellular application of gene-engineered antibodies, aimed at ablating the abnormal function of intracellular molecules. Parkinson's disease (PD) is a common neurodegenerative disease with no cure. Recent studies have explored possible intrabody applications against alpha-synuclein (alpha-syn), whose misfolding is believed to cause a familial form of PD. Here, we review the origin, production, and therapeutic mechanisms of intrabodies and the potential of intrabody protection against alpha-syn toxicity. Furthermore, we propose possible intrabody applications against leucine-rich repeat kinase 2 (LRRK2), whose mutations are the most frequent known cause of familial and sporadic PD.

Indexed as

Genetic Therapyalpha-SynucleinAnimalsAntibodiesHumansParkinson DiseaseProtein Engineeringalpha-SynucleinAntibodies

Identifiers

PMID18834937
PMCPMC2745095

What OpenQuestion holds

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Registered trials

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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.