Evidence map›Paper›PMID 28271030›Full record

ArticleMolecular metabolism2017

High-fidelity

Amanda M Ackermann, Jia Zhang, Aryel Heller, Anna Briker, Klaus H Kaestner

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 61 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Amanda M AckermannDivision of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, 3400 Civic Center Boulevard, Philadelphia, PA, 19104, USA; Institute of Diabetes, Obesity, and Metabolism, Perelman School of Medicine, The University of Pennsylvania, 3400 Civic Center Boulevard, Philadelphia, PA, 19104, USA. Electronic address: ackermanna@email.chop.edu.
Jia ZhangInstitute of Diabetes, Obesity, and Metabolism, Perelman School of Medicine, The University of Pennsylvania, 3400 Civic Center Boulevard, Philadelphia, PA, 19104, USA; Department of Genetics, Perelman School of Medicine, The University of Pennsylvania, 3400 Civic Center Boulevard, Philadelphia, PA, 19104, USA. Electronic address: zhangjia@upenn.edu.
Aryel HellerInstitute of Diabetes, Obesity, and Metabolism, Perelman School of Medicine, The University of Pennsylvania, 3400 Civic Center Boulevard, Philadelphia, PA, 19104, USA; Department of Genetics, Perelman School of Medicine, The University of Pennsylvania, 3400 Civic Center Boulevard, Philadelphia, PA, 19104, USA. Electronic address: aryelh@mail.med.upenn.edu.
Anna BrikerDepartment of Genetics, Perelman School of Medicine, The University of Pennsylvania, 3400 Civic Center Boulevard, Philadelphia, PA, 19104, USA. Electronic address: abriker@villanova.edu.
Klaus H KaestnerInstitute of Diabetes, Obesity, and Metabolism, Perelman School of Medicine, The University of Pennsylvania, 3400 Civic Center Boulevard, Philadelphia, PA, 19104, USA; Department of Genetics, Perelman School of Medicine, The University of Pennsylvania, 3400 Civic Center Boulevard, Philadelphia, PA, 19104, USA. Electronic address: kaestner@mail.med.upenn.edu.
University of Pennsylvania · USChildren's Hospital of Philadelphia · US

Funding

VIRAL VECTOR COREP30DK019525 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI MITCHELL A. LAZAR · 1986 to 2026
$48.3M
TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell · 1997 to 2026
$32.5M
ZINC FINGER PROTEINS IN EARLY KIDNEY DEVELOPMENTP01DK049210 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI AHIMA, REXFORD S. · 1995 to 2016
$26.9M
Epigenetic Rejuvenation of Human Beta-CellsUC4DK104119 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI GLASER, BENJAMIN, KAESTNER, KLAUS H · 2014 to 2014
$3.6M
NIDDK NIH HHS P01 DK049210NIDDK NIH HHS P30 DK019525NIDDK NIH HHS P30 DK050306NIDDK NIH HHS UC4 DK104119
6 · The paper itself

Abstract

objectiveα-cells are the second most prominent cell type in pancreatic islets and are responsible for producing glucagon to increase plasma glucose levels in times of fasting. α-cell dysfunction and inappropriate glucagon secretion occur in both type 1 and type 2 diabetes. Thus, there is growing interest in studying both normal function and pathophysiology of α-cells. However, tools to target gene ablation or activation specifically of α-cells have been limited, compared to those available for β-cells. Previous

methodsWe utilized CRISPR-Cas9 technology to insert an

resultsTamoxifen injection of

conclusionsWe successfully derived a

Indexed as

3' Untranslated RegionsAnimalsCRISPR-Cas SystemsDiabetes Mellitus, Type 2Gene Knock-In TechniquesGene TargetingGenetic EngineeringGenetic TechniquesGlucagonGlucagon-Secreting CellsIslets of LangerhansMiceMice, TransgenicTamoxifenTransgenes3' Untranslated RegionsGlucagonTamoxifenCre, Cre recombinaseCreERT2, tamoxifen-inducible Cre recombinase-estrogen receptor fusion proteinCRISPRCRISPR, clustered regularly interspaced short palindromic repeatDAPI, 4′,6-diamidino-2-phenylindoleEnteroendocrine L-cellESC, embryonic stem cellFACS, fluorescence-activated cell sortingGCG, glucagonGLP1GLP1, glucagon-like peptide 1GlucagongRNA, guide RNAIRES, internal ribosomal entry siteIsletLSL, loxP-stop-loxPUTR, untranslated regionYFP, yellow fluorescent proteinα-cell

Identifiers

PMID28271030
PMCPMC5323890
OpenAlexW2573896876

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.