Evidence map›Paper›PMID 18508467›Full record

ReviewFrontiers in bioscience : a journal and virtual library2008

Molecular analysis of early host cell infection by Trypanosoma cruzi.

Fernando Villalta, M Nia Madison, Yuliya Y Kleshchenko, Pius N Nde, Maria F Lima

Open access · bronzeAbstract readReview
In one paragraph

Review in Frontiers in bioscience : a journal and virtual library, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.0field-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

15 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. New insights intoFrontiers in immunology · 2024
    Review
  3. Mechanisms Associated withLife (Basel, Switzerland) · 2021
    Review
  4. Review
  5. Article
  6. Frontiers in microbiology · 2017
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review on Trypanosoma cruzi: Host Cell Interaction.International journal of cell biology · 2010
    Article
  14. Review
  15. 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

5 authors at 1 institution in 1 country.

Fernando VillaltaDepartment of Microbial Pathogenesis and Immune Response, School of Medicine, Meharry Medical College, 1005 Dr. D.B. Todd Jr. Blvd., Nashville, TN 37208-3599, USA. fvillalta@mmc.edu
M Nia Madison
Yuliya Y Kleshchenko
Pius N Nde
Maria F Lima
Meharry Medical College · US

Funding

THE MEHARRY RISE INITIATIVER25GM059994 · NIGMS · MEHARRY MEDICAL COLLEGE · PI MOTLEY-JOHNSON, EVANGELINE D · 1999 to 2021
$23.0M
THE MOLECULAR BASIS OF BARTONELLA BACILLIFORMIS PATHOGENICITYS06GM008037 · NIGMS · MEHARRY MEDICAL COLLEGE · PI RUCKER, HUBERT K. · 1989 to 2007
$17.5M
Research Training in Cardivascular Biology at MeharryT32HL007737 · NHLBI · MEHARRY MEDICAL COLLEGE · PI MARTIN, PAMELA M · 1993 to 2025
$4.7M
MOLECULAR PARASITOLOGY TRAINING PROGRAMT32AI007281 · NIAID · MEHARRY MEDICAL COLLEGE · PI NDE, PIUS N · 1985 to 2025
$3.2M
Molecular Analysis of Trypanosome InfectionSC1AI080580 · NIAID · MEHARRY MEDICAL COLLEGE · PI VILLALTA, FERNANDO · 2008 to 2010
$1.1M
Molecular Analysis of Trypanosome InfectionSC1GM081168 · NIGMS · MEHARRY MEDICAL COLLEGE · PI VILLALTA, FERNANDO · 2007 to 2007
$366k
MARC TRAINING PROGRAM AT PEMBROKE STATE UNIVERSITYT34GM008037 · NIGMS · UNIVERSITY OF NORTH CAROLINA AT PEMBROKE · PI WORIAX, VELINDA L · 1985 to 2000
$42k
NHLBI NIH HHS HL 007737NHLBI NIH HHS T32 HL007737NIAID NIH HHS AI 007281NIAID NIH HHS SC1 AI080580NIAID NIH HHS T32 AI007281NIGMS NIH HHS GM 008037NIGMS NIH HHS GM 081168NIGMS NIH HHS R25 GM059994NIGMS NIH HHS S06 GM008037NIGMS NIH HHS SC1 GM081168
6 · The paper itself

Abstract

Trypanosoma cruzi, the causative agent of Chagas heart disease, infects heart and other cells leading to cardiac arrest frequently followed by death. The disease affects millions of individuals in the Americas and is posing health problems because of blood transmission in the US due to large Latin American immigration. Since the current drugs present serious side effects and do not cure the chronic infection, it is critically important to understand the early process of cellular infection at the molecular and structural levels to design novel inhibitors to block T. cruzi infection. In this review, the authors critically analyze the molecular and cellular basis of early T. cruzi infection and discuss the future directions in this area. The candidate T. cruzi invasive genes and host genes involved in the process of early infection are just beginning to be understood. The trypanosome invasive proteins are excellent targets for intervention. The progress made in the cell biology of T. cruzi infection will also facilitate the development of novel cell-based therapies to ameliorate the disease.

Indexed as

AnimalsCasein Kinase IIChagas DiseaseCysteine EndopeptidasesGlycoproteinsHost-Parasite InteractionsHumansNeuraminidaseProlyl OligopeptidasesProtozoan ProteinsSerine EndopeptidasesTrypanosoma cruziCasein Kinase IIcruzipainCysteine EndopeptidasesGlycoproteinsNeuraminidasePREPL protein, humanProlyl OligopeptidasesProtozoan ProteinsSerine Endopeptidasestrans-sialidase

Identifiers

PMID18508467
PMCPMC2728773
OpenAlexW1969756292

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.