Evidence map›Paper›PMID 29109113›Full record

ArticleDrug metabolism and disposition: the biological fate of chemicals2018

Generation and Characterization of SULT4A1 Mutant Mouse Models.

Patrick L Garcia, Mohammed I Hossain, Shaida A Andrabi, Charles N Falany

Open access · bronzeAbstract read
In one paragraph

Article in Drug metabolism and disposition: the biological fate of chemicals, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. SULT4A1 Modulates Synaptic Development and Function by Promoting the Formation of PSD-95/NMDAR Complex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  13. SULT4A1 Protects Against Oxidative-Stress Induced Mitochondrial Dysfunction in Neuronal Cells.Drug metabolism and disposition: the biological fate of chemicals · 2019
    Article
  14. Sulfation pathways from red to green.The Journal of biological chemistry · 2019
    Review
  15. Sulfotransferase 4A1 Increases Its Expression in Mouse Neurons as They Mature.Drug metabolism and disposition: the biological fate of chemicals · 2018
    Article
  16. Animal Models of Tremor: Relevance to Human Tremor Disorders.Tremor and other hyperkinetic movements (New York, N.Y.) · 2018
    Review
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

4 authors at 1 institution in 1 country.

Patrick L GarciaDepartment of Pharmacology and Toxicology, and Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama.
Mohammed I HossainDepartment of Pharmacology and Toxicology, and Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama.
Shaida A AndrabiDepartment of Pharmacology and Toxicology, and Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama.
Charles N FalanyDepartment of Pharmacology and Toxicology, and Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama cfalany@uab.edu.
University of Alabama at Birmingham · US

Funding

Poly (ADP-ribose) Mediates Cell Death in Stroke by Inhibiting Glucose MetabolismR01NS086953 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ANDRABI, SHAIDA A. · 2015 to 2019
$1.7M
SULT4A1 in Zebrafish DevelopmentR01GM113980 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FALANY, CHARLES N · 2015 to 2017
$838k
NIGMS NIH HHS R01 GM113980NINDS NIH HHS R01 NS086953
6 · The paper itself

Abstract

Sulfotransferase 4A1 (SULT4A1) belongs to the cytosolic sulfotransferase (SULT) superfamily of enzymes that catalyze sulfonation reactions with a variety of endogenous and exogenous substrates. Of the SULTs, SULT4A1 was shown to have the highest sequence homology between vertebrate species, yet no known function or enzymatic activity has been identified for this orphan SULT. To better understand SULT4A1 function in mammalian brain, two mutant SULT4A1 mouse strains were generated utilizing clustered regulatory interspaced short palindromic repeats (CRISPR)-content-addressable storage (Cas) 9 technology. The first strain possessed a 28-base pair (bp) deletion (Δ28) in exon 1 that resulted in a frameshift mutation with premature termination. The second strain possessed a 12-bp in-frame deletion (Δ12) immediately preceding an active site histidine

Indexed as

AnimalsBehavior, AnimalBrainCRISPR-Cas SystemsCytosolExonsFemaleFrameshift MutationHomozygoteMaleMiceMice, Inbred C57BLModels, AnimalNerve Tissue ProteinsNeuronsPrimary Cell CultureNerve Tissue ProteinsSulfotransferases

Identifiers

PMID29109113
PMCPMC5733458
OpenAlexW2768013634

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.