Evidence map›Paper›PMID 15585659›Full record

ArticleNucleic acids research2004

A mammalian artificial chromosome engineering system (ACE System) applicable to biopharmaceutical protein production, transgenesis and gene-based cell therapy.

Michael Lindenbaum, Ed Perkins, Erika Csonka, Elena Fleming, Lisa Garcia, Amy Greene, Lindsay Gung, Gyula Hadlaczky, Edmond Lee, Josephine Leung and 11 more

Open access · greenAbstract read
In one paragraph

Article in Nucleic acids research, 2004. 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
7.0field-weighted citation impact, top 3% 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, 137 citations in OpenAlex.

  1. Article
  2. Article
  3. A pathway from chromosome transfer to engineering resulting in human and mouse artificial chromosomes for a variety of applications to bio-medical challenges.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2015
    Review
  4. De novo formed satellite DNA-based mammalian artificial chromosomes and their possible applications.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2015
    Review
  5. Article
  6. Chromosomes in the flow to simplify genome analysis.Functional & integrative genomics · 2012
    Review
  7. Article
  8. Human artificial chromosomes for gene delivery and the development of animal models.Molecular therapy : the journal of the American Society of Gene Therapy · 2011
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Use of transgenic animals to improve human health and animal production.Reproduction in domestic animals = Zuchthygiene · 2005
    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

21 authors at 1 institution in 1 country.

Michael LindenbaumChromos Molecular Systems, Inc., 8081 Lougheed Highway, Burnaby, BC, Canada V5A 1W9.
Ed Perkins
Erika Csonka
Elena Fleming
Lisa Garcia
Amy Greene
Lindsay Gung
Gyula Hadlaczky
Edmond Lee
Josephine Leung
Neil MacDonald
Alexisann Maxwell
Kathleen Mills
Diane Monteith
Carl F Perez
Joan Shellard
Sandy Stewart
Tom Stodola
Dana Vandenborre
Sandy Vanderbyl
Harry C Ledebur
D-Wave Systems (Canada) · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mammalian artificial chromosomes (MACs) provide a means to introduce large payloads of genetic information into the cell in an autonomously replicating, non-integrating format. Unique among MACs, the mammalian satellite DNA-based Artificial Chromosome Expression (ACE) can be reproducibly generated de novo in cell lines of different species and readily purified from the host cells' chromosomes. Purified mammalian ACEs can then be re-introduced into a variety of recipient cell lines where they have been stably maintained for extended periods in the absence of selective pressure. In order to extend the utility of ACEs, we have established the ACE System, a versatile and flexible platform for the reliable engineering of ACEs. The ACE System includes a Platform ACE, containing >50 recombination acceptor sites, that can carry single or multiple copies of genes of interest using specially designed targeting vectors (ATV) and a site-specific integrase (ACE Integrase). Using this approach, specific loading of one or two gene targets has been achieved in LMTK(-) and CHO cells. The use of the ACE System for biological engineering of eukaryotic cells, including mammalian cells, with applications in biopharmaceutical production, transgenesis and gene-based cell therapy is discussed.

Indexed as

Chromosomes, Artificial, MammalianAnimalsAnimals, Genetically ModifiedCell LineCHO CellsCricetinaeCricetulusDrug IndustryErythropoietinGenetic EngineeringGenetic TherapyHumansIntegrasesMiceMice, Inbred NODMice, SCIDErythropoietinIntegrasesRecombinant Proteins

Identifiers

PMID15585659
PMCPMC535698
OpenAlexW2097496703

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.