Evidence map›Paper›PMID 24563304›Full record

ArticleBiotechnology letters2014

Generation of a cre recombinase-conditional Nos1ap over-expression transgenic mouse.

Dallas R Auer, Polina Sysa-Shah, Djahida Bedja, Jessica L Simmers, Evgenia Pak, Amalia Dutra, Ronald Cohn, Kathleen L Gabrielson, Aravinda Chakravarti, Ashish Kapoor

Open access · greenAbstract read
In one paragraph

Article in Biotechnology letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. DifferentialScience advances · 2026
    Article
  2. Article
  3. 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

10 authors at 5 institutions in 2 countries.

Dallas R AuerMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, 733 N. Broadway, Baltimore, MD, 21205, USA, dallas@jhmi.edu.
Polina Sysa-Shah
Djahida Bedja
Jessica L Simmers
Evgenia Pak
Amalia Dutra
Ronald Cohn
Kathleen L Gabrielson
Aravinda Chakravarti
Ashish Kapoor
Johns Hopkins University · USJohns Hopkins Medicine · USHospital for Sick Children · CANational Human Genome Research Institute · USNational Institutes of Health · US

Funding

Genome-Wide Association Analysis in Essential Hypertension (FEHGAS study)R01HL086694 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ARAVINDA CHAKRAVARTI · 2007 to 2026
$21.2M
NHGRI/DIR Cytogenetics and Microscopy CoreZICHG200348 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI WINCOVITCH, STEPHEN · 2010 to 2025
$20.3M
GWAS TO GENE FUNCTION: NOS1AP AND OTHER QT INTERVAL GENESR01GM104469 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CHAKRAVARTI, ARAVINDA · 2014 to 2017
$2.5M
NHLBI NIH HHS R01 HL086694NIGMS NIH HHS R01 GM104469
6 · The paper itself

Abstract

Polymorphic non-coding variants at the NOS1AP locus have been associated with the common cardiac, metabolic and neurological traits and diseases. Although, in vitro gene targeting-based cellular and biochemical studies have shed some light on NOS1AP function in cardiac and neuronal tissue, to enhance our understanding of NOS1AP function in mammalian physiology and disease, we report the generation of cre recombinase-conditional Nos1ap over-expression transgenic mice (Nos1ap (Tg)). Conditional transgenic mice were generated by the pronuclear injection method and three independent, single-site, multiple copies integration event-based founder lines were selected. For heart-restricted over-expression, Nos1ap (Tg) mice were crossed with Mlc2v-cre and Nos1ap transcript over-expression was observed in left ventricles from Nos1ap (Tg); Mlc2v-cre F1 mice. We believe that with the potential of conditional over-expression, Nos1ap (Tg) mice will be a useful resource in studying NOS1AP function in various tissues under physiological and disease states.

Indexed as

Gene ExpressionMice, TransgenicAdaptor Proteins, Signal TransducingAnimalsCrosses, GeneticIntegrasesRecombination, GeneticAdaptor Proteins, Signal TransducingCre recombinaseIntegrasesNos1ap protein, mouse

Identifiers

PMID24563304
PMCPMC4850732
OpenAlexW2119670156

What OpenQuestion holds

Textmetadata
LicenceTDM
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.