Evidence map›Paper›PMID 19995283›Full record

ArticleOligonucleotides2010

Sequence-specific correction of genomic hypoxanthine-guanine phosphoribosyl transferase mutations in lymphoblasts by small fragment homologous replacement.

Babak Bedayat, Alireza Abdolmohamadi, Lin Ye, Rosalie Maurisse, Hooman Parsi, Jennifer Schwarz, Hamid Emamekhoo, Janice A Nicklas, J Patrick O'Neill, Dieter C Gruenert

Open access · greenAbstract read
In one paragraph

Article in Oligonucleotides, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  4. Review
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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

10 authors at 3 institutions in 1 country.

Babak BedayatCalifornia Pacific Medical Center Research Institute, San Francisco, California 94107, USA.
Alireza Abdolmohamadi
Lin Ye
Rosalie Maurisse
Hooman Parsi
Jennifer Schwarz
Hamid Emamekhoo
Janice A Nicklas
J Patrick O'Neill
Dieter C Gruenert
California Pacific Medical Center · USUniversity of California, San Francisco · USUniversity of Vermont · US

Funding

BASIC RESEARCH IN HEMATOLOGY AND ONCOLOGYT32DK007636 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SHUMAN, MARC A. · 1989 to 2013
$2.7M
CHARACTERIZATION OF SFHR MODIFICATION OF GENOMIC HPRTR01GM075111 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRUENERT, DIETER C · 2007 to 2010
$1.3M
Generation of a CF Pig by SFHR and Nuclear TransferR21DK066403 · NIDDK · CALIFORNIA PACIFIC MED CTR RES INSTITUTE · PI GRUENERT, DIETER C · 2004 to 2005
$320k
NIDDK NIH HHS R21 DK66403NIDDK NIH HHS T32 DK007636NIGMS NIH HHS R01 GM075111NIGMS NIH HHS R01 GM75111
6 · The paper itself

Abstract

Oligo/polynucleotide-based gene targeting strategies provide new options for achieving sequence-specific modification of genomic DNA and have implications for the development of new therapies and transgenic animal models. One such gene modification strategy, small fragment homologous replacement (SFHR), was evaluated qualitatively and quantitatively in human lymphoblasts that contain a single base substitution in the hypoxanthine-guanine phosphoribosyl transferase (HPRT1) gene. Because HPRT1 mutant cells are readily discernable from those expressing the wild type (wt) gene through growth in selective media, it was possible to identify and isolate cells that have been corrected by SFHR. Transfection of HPRT1 mutant cells with polynucleotide small DNA fragments (SDFs) comprising wild type HPRT1 (wtHPRT1) sequences resulted in clones of cells that grew in hypoxanthine-aminopterin-thymidine (HAT) medium. Initial studies quantifying the efficiency of correction in 3 separate experiments indicate frequencies ranging from 0.1% to 2%. Sequence analysis of DNA and RNA showed correction of the HPRT1 mutation. Random integration was not indicated after transfection of the mutant cells with an SDF comprised of green fluorescent protein (GFP) sequences that are not found in human genomic DNA. Random integration was also not detected following Southern blot hybridization analysis of an individual corrected cell clone.

Indexed as

GenomicsMutationBase SequenceCells, CulturedCulture MediaDNA PrimersGreen Fluorescent ProteinsHumansHypoxanthine PhosphoribosyltransferaseLymphocytesMaleMolecular Sequence DataSequence Analysis, DNACulture MediaDNA PrimersGreen Fluorescent ProteinsHypoxanthine Phosphoribosyltransferase

Identifiers

PMID19995283
PMCPMC2948462
OpenAlexW2030844139

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.