Evidence map›Paper›PMID 9653145›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1998

Targeted expansion of genetically modified bone marrow cells.

L Jin, N Siritanaratkul, D W Emery, R E Richard, K Kaushansky, T Papayannopoulou, C A Blau

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. 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
2.9field-weighted citation impact, top 9% 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, 72 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Long-term regulation of genetically modified primary hematopoietic cells in dogs.Molecular therapy : the journal of the American Society of Gene Therapy · 2011
    Article
  6. Gene therapy of MPL deficiency: challenging balance between leukemia and pancytopenia.Molecular therapy : the journal of the American Society of Gene Therapy · 2010
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Hematopoietic stem cell gene therapy.International journal of hematology · 2002
    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

7 authors at 1 institution in 1 country.

L JinDivision of Hematology, Mailstop 357710, Health Sciences Building, University of Washington, Seattle WA 98195, USA. tblau@u.washington.edu
N Siritanaratkul
D W Emery
R E Richard
K Kaushansky
T Papayannopoulou
C A Blau
University of Washington · US

Funding

VECTOR CONSTRUCTIONS FOR GENE THERAPY OF SICKLE CELL DISEASEP01HL053750 · NHLBI · UNIVERSITY OF WASHINGTON · PI RUSSELL, DAVID W · 1994 to 2014
$30.4M
PILOT STUDY--RETROVIRUS MEDIATED TRANSFER OF HUMAN GLUCOCEREBROSIDASE GENEP30DK047754 · NIDDK · UNIVERSITY OF WASHINGTON · PI MILLER, ARTHUR DUSTY · 1994 to 2008
$8.4M
PROLIFERATIVE SWITCH FOR GENETICALLY MODIFIED CELLSR01DK052997 · NIDDK · UNIVERSITY OF WASHINGTON · PI BLAU, C. ANTHONY · 1997 to 2004
$1.3M
NHLBI NIH HHS 5P01 HL53750NHLBI NIH HHS P01 HL053750NIDDK NIH HHS 1R01 DK52997-01NIDDK NIH HHS 5P30 DK47754NIDDK NIH HHS P30 DK047754NIDDK NIH HHS R01 DK052997
6 · The paper itself

Abstract

The ability to specifically target a mitogenic signal to a population of genetically modified primary cells would have potential applications both for gene and cell therapy. Toward this end, a gene encoding a fusion protein containing the FK506-binding protein FKBP12, fused to the intracellular portion of the receptor for thrombopoietin (mpl), was introduced into primary murine bone marrow cells. Dimerization of this fusion protein through the addition of a dimeric form of the drug FK506, called FK1012, resulted in a marked proliferative expansion of marrow cells that was restricted to the genetically modified population. FK1012's proliferative effect was sustained and reversible. An apparent preference for differentiation along the megakaryocytic lineage was observed. This approach allows for the specific delivery of a mitogenic signal to a population of genetically modified primary cells and may have applications for studies in hematopoiesis and receptor biology, and for gene and cell therapy.

Indexed as

Gene Transfer TechniquesNeoplasm ProteinsReceptors, CytokineAnimalsBone Marrow CellsCarrier ProteinsCell DivisionCell LineageDNA-Binding ProteinsGenetic TherapyHeat-Shock ProteinsHematopoiesisMiceProto-Oncogene ProteinsReceptors, ThrombopoietinRecombinant Fusion ProteinsCarrier ProteinsDNA-Binding ProteinsHeat-Shock ProteinsMPL protein, humanNeoplasm ProteinsProto-Oncogene ProteinsReceptors, CytokineReceptors, ThrombopoietinRecombinant Fusion ProteinsTacrolimus Binding Proteins

Identifiers

PMID9653145
PMCPMC20934
OpenAlexW2076088666

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.