Failure of glycine site NMDA receptor antagonists to protect against L-2-chloropropionic acid-induced neurotoxicity highlights the uniqueness of cerebellar NMDA receptors. (Q48864470)

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English	Failure of glycine site NMDA receptor antagonists to protect against L-2-chloropropionic acid-induced neurotoxicity highlights the uniqueness of cerebellar NMDA receptors.	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

Failure of glycine site NMDA receptor antagonists to protect against L-2-chloropropionic acid-induced neurotoxicity highlights the uniqueness of cerebellar NMDA receptors. (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

1 reference

based on heuristic

inferred from title

(-)-2-chloropropionic acid

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ChEBI release 2020-05-28

toxic encephalopathy

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based on heuristic

inferred from title

author name string

Widdowson PS

1

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

Gyte AJ

2

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

Upton R

3

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

Wyatt I

4

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

language of work or name

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publication date

1 November 1996

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

number of pages

7

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inferred from page(s)

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

738

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

2

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

236-242

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

Transfection of N-methyl-D-aspartate receptors in a nonneuronal cell line leads to cell death

1 reference

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Differential expression of five N-methyl-D-aspartate receptor subunit mRNAs in the cerebellum of developing and adult rats.

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NMDA-receptor channel diversity in the developing cerebellum.

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Pharmacological modification of glutamate neurotoxicity in vivo

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Ionic requirements for neurotoxic effects of excitatory amino acid analogues in rat cerebellar slices.

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Reversible and irreversible neuronal damage caused by excitatory amino acid analogues in rat cerebellar slices.

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Glycine potentiates the NMDA response in cultured mouse brain neurons

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Neuroprotection by the N-methyl-D-aspartate receptor antagonist CGP 40116: in vivo and in vitro studies

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Differential stimulation of [3H]MK-801 binding to subpopulations of NMDA receptors

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Heteromeric NMDA receptors: molecular and functional distinction of subtypes

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Evidence for heterogenous glycine domains but conserved multiple states of the excitatory amino acid recognition site of the NMDA receptor: regional binding studies with [3H]glycine and [3H]L-glutamate

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Whole cell and single channel analysis of the kinetics of glycine-sensitive N-methyl-D-aspartate receptor desensitization

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Selective neuronal vulnerability: morphological and molecular characteristics.

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3-Acyl-4-hydroxyquinolin-2(1H)-ones. Systemically active anticonvulsants acting by antagonism at the glycine site of the N-methyl-D-aspartate receptor complex

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[3H]thienyl-phencyclidine ([3H]TCP) binds to two different sites in rat brain. Localization by autoradiographic and biochemical techniques

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NMDA receptors in rat cerebellum and forebrain: subtle differences in pharmacology and modulation

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[125I]endothelin binding in rat cerebellum is increased following L-2-chloropropionic-acid-induced granule cell necrosis

1 reference

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7 January 2021

Identifiers

10.1016/S0006-8993(96)00779-2

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8955518

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