Evidence map›Paper›PMID 11296261›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

In vivo detection of gene expression in liver by 31P nuclear magnetic resonance spectroscopy employing creatine kinase as a marker gene.

A Auricchio, R Zhou, J M Wilson, J D Glickson

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Development of Timd2 as a reporter gene for MRI.Magnetic resonance in medicine · 2016
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. In Vivo Noninvasive Imaging for Gene Therapy.Journal of biomedicine & biotechnology · 2003
    Article
  12. Noninvasive real-time imaging of apoptosis.Proceedings of the National Academy of Sciences of the United States of America · 2002
    Article
  13. Review
  14. 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.

A AuricchioDepartment of Molecular and Cellular Engineering, Institute for Human Gene Therapy, University of Pennsylvania, Philadelphia, PA 19104, USA.
R Zhou
J M Wilson
J D Glickson
The Wistar Institute · USUniversity of Pennsylvania · US

Funding

Vector CoreP30DK047757 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI WILSON, JAMES M · 1993 to 2017
$18.0M
SMALL ANIMAL MULTIMODALITY IMAGING CENTER (SAMMIC)R24CA083105 · NCI · UNIVERSITY OF PENNSYLVANIA · PI GLICKSON, JERRY D · 1999 to 2003
$2.2M
MID-ATLANTIC IN VIVO CELLULAR &MOLECULAR IMAGING CENTERP20CA086255 · NCI · UNIVERSITY OF PENNSYLVANIA · PI GLICKSON, JERRY D · 2000 to 2002
$1.1M
NCI NIH HHS P20 CA86255NCI NIH HHS R24 CA083105NCI NIH HHS R24 CA83105NIDDK NIH HHS P30 DK047757NIDDK NIH HHS P30 DK47757Telethon 371/B
6 · The paper itself

Abstract

In vivo assessment of gene expression is desirable to obtain information on the extent and duration of transduction of tissue after gene delivery. We have developed an in vivo, potentially noninvasive, method for detecting virally mediated gene transfer to the liver. The method employs an adenoviral vector carrying the gene for the brain isozyme of murine creatine kinase (CK-B), an ATP-buffering enzyme expressed mainly in muscle and brain but absent from liver, kidney, and pancreas. Gene expression was monitored by (31)P magnetic resonance spectroscopy (MRS) using the product of the CK enzymatic reaction, phosphocreatine, as an indicator of transfection. The vector was administered into nude mice by tail vein injection, and exogenous creatine was administered in the drinking water and by i.p. injection of 2% creatine solution before (31)P MRS examination, which was performed on surgically exposed livers. A phosphocreatine resonance was detected in livers of mice injected with the vector and was absent from livers of control animals. CK expression was confirmed in the injected animals by Western blot analysis, enzymatic assays, and immunofluorescence measurements. We conclude that the syngeneic enzyme CK can be used as a marker gene for in vivo monitoring of gene expression after virally mediated gene transfer to the liver.

Indexed as

Magnetic Resonance SpectroscopyAdenoviridaeAnimalsBlotting, WesternBrainCell ExtractsCreatineCreatine KinaseFemaleFluorescent Antibody TechniqueGene ExpressionGenes, ReporterGenetic VectorsGene Transfer TechniquesIsoenzymesLiverCell ExtractsCreatineCreatine KinaseIsoenzymesPhosphocreatine

Identifiers

PMID11296261
PMCPMC33188
OpenAlexW2000906654

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.