Evidence map›Paper›PMID 34097949›Full record

ReviewNeuropharmacology2021

Regulation of the NMDA receptor by its cytoplasmic domains: (How) is the tail wagging the dog?

Yevheniia Ishchenko, Melissa G Carrizales, Anthony J Koleske

Open access · greenAbstract readReview
In one paragraph

Review in Neuropharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Lasting effects of early-life oxytocin treatment on LTP and episodic memory in a mouse model of Fragile X syndrome.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. CaNature plants · 2024
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Protein quality control ofFrontiers in cellular neuroscience · 2022
    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

3 authors at 1 institution in 1 country.

Yevheniia IshchenkoDepartments of Molecular Biophysics and Biochemistry and Neuroscience, Yale School of Medicine, Yale University, United States. Electronic address: yevheniia.ishchenko@yale.edu.
Melissa G CarrizalesDepartments of Molecular Biophysics and Biochemistry and Neuroscience, Yale School of Medicine, Yale University, United States.
Anthony J KoleskeDepartments of Molecular Biophysics and Biochemistry and Neuroscience, Yale School of Medicine, Yale University, United States.
Yale University · US

Funding

Impact of excitatory synapse maturation on synaptic plasticity and stabilityR01NS105640 · NINDS · YALE UNIVERSITY · PI HIGLEY, MICHAEL JAMES, KOLESKE, ANTHONY J · 2018 to 2022
$2.5M
Control of Dendritic Spine Stability via Regulation of a Stable Actin PoolR01MH115939 · NIMH · YALE UNIVERSITY · PI KOLESKE, ANTHONY J · 2018 to 2022
$2.2M
The role of TRIO signaling in neuronal development, synaptic function, and circuit connectivityR56MH122449 · NIMH · YALE UNIVERSITY · PI CARDIN, JESSICA A, HIGLEY, MICHAEL JAMES · 2021 to 2022
$1.4M
Direct binding and control of microtubule elongation by Abl2R21NS112121 · NINDS · YALE UNIVERSITY · PI KOLESKE, ANTHONY J · 2020 to 2020
$459k
NIMH NIH HHS R01 MH115939NIMH NIH HHS R56 MH122449NINDS NIH HHS R01 NS105640NINDS NIH HHS R21 NS112121
6 · The paper itself

Abstract

Excitatory neurotransmission mediated by N-methyl-d-aspartate receptors (NMDARs) is critical for synapse development, function, and plasticity in the brain. NMDARs are tetra-heteromeric cation-channels that mediate synaptic transmission and plasticity. Extensive human studies show the existence of genetic variants in NMDAR subunits genes (GRIN genes) that are associated with neurodevelopmental and neuropsychiatric disorders, including autism spectrum disorders (ASD), epilepsy (EP), intellectual disability (ID), attention deficit hyperactivity disorder (ADHD), and schizophrenia (SCZ). NMDAR subunits have a unique modular architecture with four semiautonomous domains. Here we focus on the carboxyl terminal domain (CTD), also known as the intracellular C-tail, which varies in length among the glutamate receptor subunits and is the most diverse domain in terms of amino acid sequence. The CTD shows no sequence homology to any known proteins but encodes short docking motifs for intracellular binding proteins and covalent modifications. Our review will discuss the many important functions of the CTD in regulating NMDA membrane and synaptic targeting, stabilization, degradation targeting, allosteric modulation and metabotropic signaling of the receptor. This article is part of the special issue on 'Glutamate Receptors - NMDA Receptors'.

Indexed as

AnimalsCytoplasmNeuronal PlasticityReceptors, N-Methyl-D-AspartateSignal TransductionSynaptic TransmissionReceptors, N-Methyl-D-AspartateCTDGluNGluN2BGlutamate receptorIntracellular C-TailNMDA receptor

Identifiers

PMID34097949
PMCPMC8410658
OpenAlexW3166855948

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.