Evidence map›Paper›PMID 25083578›Full record

ArticleACS chemical neuroscience2014

The postnatal development of D-serine in the retinas of two mouse strains, including a mutant mouse with a deficiency in D-amino acid oxidase and a serine racemase knockout mouse.

Gabriel E Romero, Amber D Lockridge, Catherine W Morgans, Dipankar Bandyopadhyay, Robert F Miller

Abstract read
In one paragraph

Article in ACS chemical neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Identity of the NMDA receptor coagonist is synapse specific and developmentally regulated in the hippocampus.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  9. Regulation of Aqueous Humor Dynamics by Hydrogen Sulfide: Potential Role in Glaucoma Pharmacotherapy.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics
    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

5 authors at 1 institution in 1 country.

Gabriel E RomeroDepartment of Neuroscience, and ‡Division of Biostatistics, School of Public Health, University of Minnesota , Minneapolis, Minnesota 55455, United States.
Amber D Lockridge
Catherine W Morgans
Dipankar Bandyopadhyay
Robert F Miller
Oregon Health & Science University · US

Funding

Cell Communication of the Vertebrate RetinaR01EY003014 · NEI · WASHINGTON UNIVERSITY · PI MILLER, ROBERT FRANCIS · 1985 to 2012
$4.7M
The cell types and mechanisms of D-serine release in the postnatal retinaR21EY025027 · NEI · UNIVERSITY OF MINNESOTA · PI MILLER, ROBERT FRANCIS · 2015 to 2016
$430k
NEI NIH HHS R01 EY003014NEI NIH HHS R01-EY03014NEI NIH HHS R21 EY025027
6 · The paper itself

Abstract

D-Serine, an N-methyl D-aspartate receptor coagonist, and its regulatory enzymes, D-amino acid oxidase (DAO; degradation) and serine racemase (SR; synthesis), have been implicated in crucial roles of the developing central nervous system, yet the functional position that they play in regulating the availability of d-serine throughout development of the mammalian retina is not well-known. Using capillary electrophoresis and a sensitive method of enantiomeric amino acid separation, we were able to determine total levels of d-serine at specific ages during postnatal development of the mouse retina in two different strains of mice, one of which contained a loss-of-function point mutation for DAO while the other was a SR knockout line. Each mouse line was tested against conspecific wild type (WT) mice for each genetic strain. The universal trend in all WT and transgenic mice was a large amount of total retinal d-serine at postnatal age 2 (P2), followed by a dramatic decrease as the mice matured into adulthood (P70-80). SR knockout mice retinas had 41% less D-serine than WT retinas at P2, and 10 times less as an adult. DAO mutant mice retinas had significantly elevated levels of d-serine when compared to WT retinas at P2 (217%), P4 (223%), P8 (194%), and adulthood (227%).

Indexed as

Age FactorsAnalysis of VarianceAnimalsAnimals, NewbornD-Amino-Acid OxidaseElectrophoresis, CapillaryGene Expression Regulation, DevelopmentalIn Vitro TechniquesMiceMice, Inbred C57BLMice, KnockoutNeurotransmitter AgentsRacemases and EpimerasesRetinaSerineSerine RacemaseD-Amino-Acid OxidaseDao1 protein, mouseNeurotransmitter AgentsRacemases and EpimerasesSerineSerine Racemasecapillary electrophoresisd-amino acid oxidased-SerineNMDA receptorretinal developmentserine racemase

Identifiers

PMID25083578
PMCPMC4176384
OpenAlexW2157023792

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.