Evidence map›Paper›PMID 36103516›Full record

ArticleScience translational medicine2022

Cold shock domain-containing protein E1 is a posttranscriptional regulator of the LDL receptor.

Geoffrey A Smith, Arun Padmanabhan, Bryan H Lau, Akhil Pampana, Li Li, Clara Y Lee, Angelo Pelonero, Tomohiro Nishino, Nandhini Sadagopan, Vivian Q Xia and 7 more

Open access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. CRISPR screening in cardiovascular research.Frontiers in cell and developmental biology · 2023
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 7 institutions in 2 countries.

Geoffrey A SmithDepartment of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0002-1638-4219
Arun PadmanabhanDivision of Cardiology, UCSF Health, San Francisco, CA 94143, USA.
Bryan H LauCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0002-0028-722X
Akhil PampanaCardiovascular Research Center, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID 0000-0002-4167-0540
Li LiDepartment of Medicine and Penn Cardiovascular Institute, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0002-7844-6120
Clara Y LeeDivision of Cardiology, UCSF Health, San Francisco, CA 94143, USA.ORCID 0000-0002-9402-4155
Angelo PeloneroGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USA.ORCID 0000-0002-7684-3771
Tomohiro NishinoGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USA.ORCID 0000-0002-3593-7368
Nandhini SadagopanDivision of Cardiology, UCSF Health, San Francisco, CA 94143, USA.
Vivian Q XiaDepartment of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0002-6540-3738
Rajan JainDepartment of Medicine and Penn Cardiovascular Institute, University of Pennsylvania, Philadelphia, PA 19104, USA.
Pradeep NatarajanCardiovascular Research Center, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID 0000-0001-8402-7435
Roland S WuDivision of Cardiology, UCSF Health, San Francisco, CA 94143, USA.ORCID 0000-0002-8253-1192
Brian L BlackCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0002-6664-8913
Deepak SrivastavaGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USA.ORCID 0000-0002-3480-5953
Kevan M ShokatDepartment of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0001-8590-7741
John S ChorbaDepartment of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0002-6397-6348
Gladstone Institutes · USUniversity of California, San Francisco · USBroad Institute · USSan Francisco General Hospital · USCalifornia Institute for Regenerative Medicine · USHoward Hughes Medical Institute · USPenn Center for AIDS Research · US

Funding

THREE DIMENSIONAL VORTEX LIKE REENTRY IN CORONARY PERFUSED VENTRICULAR WALLP01HL039707 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI JALIFE, JOSE S · 1990 to 2010
$19.0M
CARDIOGENESIS--MOLECULAR MECHANISMSR01HL057181 · NHLBI · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI DEEPAK SRIVASTAVA · 1997 to 2026
$14.0M
Project 3: Control of cardiac transcription by MEF2 and myocardinP01HL146366 · NHLBI · J. DAVID GLADSTONE INSTITUTES · PI BLACK, BRIAN L · 2019 to 2023
$13.7M
Using genetic variation to study biology of blood lipids & coronary heart diseaseR01HL127564 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Pradeep Natarajan, Gina Marie Peloso · 2015 to 2026
$7.3M
Regulation of Chromatin Signaling in Heart Failure by the BRD4 Bromodomain Protein.R01HL127240 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MCKINSEY, TIMOTHY, SRIVASTAVA, DEEPAK · 2015 to 2022
$6.4M
Clonal hematopoiesis in the Womens Health Initiative Memory StudyR01HL148565 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ALEXANDER P REINER, Eric A. Whitsel · 2019 to 2026
$5.9M
Clonal hematopoiesis in humans: determinants of development and progressionR01HL148050 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI BALLANTYNE, CHRISTIE MITCHELL, NATARAJAN, PRADEEP · 2019 to 2022
$5.9M
Whole genome sequences in individuals to comprehensively characterize the genetic mechanisms of dyslipidemiasR01HL142711 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Satoshi Koyama, Gina Marie Peloso · 2019 to 2026
$4.7M
CSDE1 as a Post Transcriptional Regulator of the LDLR - Diversity SupplementR01HL159457 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHORBA, JOHN S · 2021 to 2024
$2.6M
EXTRAMULAR RESEARCH FACILITIES CONSTRUCTIONC06RR018928 · NCRR · J. DAVID GLADSTONE INSTITUTES · PI MAHLEY, ROBERT W. · 2003 to 2003
$2.1M
Chemical Biology to Modulate PCSK9 and Treat AtherosclerosisR01HL146404 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHORBA, JOHN S · 2021 to 2024
$1.6M
The Role of BRD4 in Cardiac SpecificationR01HL139783 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI JAIN, RAJAN · 2019 to 2022
$1.6M
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NCRR NIH HHS C06 RR018928NHLBI NIH HHS K08 HL124068NHLBI NIH HHS K08 HL157700NHLBI NIH HHS P01 HL039707NHLBI NIH HHS P01 HL146366NHLBI NIH HHS R01 HL057181NHLBI NIH HHS R01 HL127240NHLBI NIH HHS R01 HL127564NHLBI NIH HHS R01 HL139783NHLBI NIH HHS R01 HL142711NHLBI NIH HHS R01 HL146404NHLBI NIH HHS R01 HL148050NHLBI NIH HHS R01 HL148565NHLBI NIH HHS R01 HL159457NHLBI NIH HHS R03 HL145259NIDDK NIH HHS R01 DK119621
6 · The paper itself

Abstract

The low-density lipoprotein receptor (LDLR) controls cellular delivery of cholesterol and clears LDL from the bloodstream, protecting against atherosclerotic heart disease, the leading cause of death in the United States. We therefore sought to identify regulators of the LDLR beyond the targets of current therapies and known causes of familial hypercholesterolemia. We found that cold shock domain-containing protein E1 (CSDE1) enhanced hepatic

Indexed as

Cold-Shock ResponseProprotein Convertase 9AnimalsDNA-Binding ProteinsHumansMiceReceptors, LDLRNA-Binding ProteinsRNA, MessengerTranscription, GeneticCSDE1 protein, humanDNA-Binding ProteinsPCSK9 protein, humanProprotein Convertase 9Receptors, LDLRNA-Binding ProteinsRNA, Messenger

Identifiers

PMID36103516
PMCPMC10174261
OpenAlexW4295786921

What Socratic 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 Socratic graph.