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Point mutation in an AMPA receptor gene rescues lethality in mice deficient in the RNA-editing enzyme ADAR2

Nature (London), 2000-07, Vol.406 (6791), p.78-81

2000

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Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy

Proceedings of the National Academy of Sciences - PNAS, 2007-10, Vol.104 (44), p.17536-17541

2007

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Voltage-independent GluN2A-type NMDA receptor Ca2+ signaling promotes audiogenic seizures, attentional and cognitive deficits in mice

Communications biology, 2021-01, Vol.4 (1), p.59-21, Article 59

2021

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Functional knock down of VCAM1 in mice mediated by endoplasmatic reticulum retained intrabodies

mAbs, 2014-11, Vol.6 (6), p.1394-1401

2014

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Generation of Rare Human NMDA Receptor Variants in Mice

Methods in molecular biology (Clifton, N.J.), 2024, Vol.2799, p.79

2024

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Author Correction: Voltage-independent GluN2A-type NMDA receptor Ca2+ signaling promotes audiogenic seizures, attentional and cognitive deficits in mice

Communications biology, 2021-02, Vol.4 (1), p.187-187, Article 187

2021

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Gene Targeted Mice with Conditional Knock-In (-Out) of NMDAR Mutations

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1677, p.201

2017

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Dysfunctions in Mice by NMDA Receptor Point Mutations NR1(N598Q) and NR1(N598R)

The Journal of neuroscience, 2000-04, Vol.20 (7), p.2558-2566

2000

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Impaired synaptic scaling in mouse hippocampal neurones expressing NMDA receptors with reduced calcium permeability

The Journal of physiology, 2005-02, Vol.562 (3), p.771-783

2005

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Developmental impact of a familial GABAA receptor epilepsy mutation

Annals of neurology, 2008-09, Vol.64 (3), p.284-293

2008

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RNA editing of AMPA receptor subunit GluR-B: A base-paired intron-exon structure determines position and efficiency

Cell, 1993-12, Vol.75 (7), p.1361-1370

1993

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Impaired Reproductive Behavior by Lack of GluR-B Containing AMPA Receptors But Not of NMDA Receptors in Hypothalamic and Septal Neurons

Molecular endocrinology (Baltimore, Md.), 2006-01, Vol.20 (1), p.219-231

2006

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Author Correction: Voltage-independent GluN2A-type NMDA receptor Ca 2+ signaling promotes audiogenic seizures, attentional and cognitive deficits in mice

Communications biology, 2021-02, Vol.4 (1), p.187

2021

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Voltage-independent GluN2A-type NMDA receptor Ca 2+ signaling promotes audiogenic seizures, attentional and cognitive deficits in mice

Communications biology, 2021-01, Vol.4 (1), p.59

2021

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Developmental impact of a familial GABA A receptor epilepsy mutation

Annals of neurology, 2008-09, Vol.64 (3), p.284-293

2008

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Developmental impact of a familial GABA sub(A) receptor epilepsy mutation

Annals of neurology, 2008-09, Vol.64 (3), p.284-293

2008

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Mice with Genetically Modified NMDA and AMPA Receptors

Annals of the New York Academy of Sciences, 1999-04, Vol.868 (1), p.494-501

1999

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Point mutation in an AMPA receptor gene lethality in mice deficient in the RNA-editing enzyme ADAR2

Nature (London), 2000-07, Vol.406 (6791), p.78-81

2000

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Functional knock down of VCAM1 in mice mediated by endoplasmatic reticulum retained intrabodies

mAbs, 2014, Vol.6 (6), p.1394-1401

2014

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Nickel decatungstate [Ni(C2H6SO)5(H2O)]2[W10O32]: Synthesis from a water-dimethylsulfoxide solution, crystal structure determination, IR and Raman spec-troscopic analysis, surface micromorphology

Žurnal strukturnoj himii, 2018, Vol.59 (1), p.149-157

2018

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Point mutation in an AMPA receptor gene rescues lethality in mice deficient in the RNA-editing enzyme ADAR2

Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy

Voltage-independent GluN2A-type NMDA receptor Ca2+ signaling promotes audiogenic seizures, attentional and cognitive deficits in mice

Functional knock down of VCAM1 in mice mediated by endoplasmatic reticulum retained intrabodies

Generation of Rare Human NMDA Receptor Variants in Mice

Author Correction: Voltage-independent GluN2A-type NMDA receptor Ca2+ signaling promotes audiogenic seizures, attentional and cognitive deficits in mice

Gene Targeted Mice with Conditional Knock-In (-Out) of NMDAR Mutations

Dysfunctions in Mice by NMDA Receptor Point Mutations NR1(N598Q) and NR1(N598R)

Impaired synaptic scaling in mouse hippocampal neurones expressing NMDA receptors with reduced calcium permeability

Developmental impact of a familial GABAA receptor epilepsy mutation

RNA editing of AMPA receptor subunit GluR-B: A base-paired intron-exon structure determines position and efficiency

Impaired Reproductive Behavior by Lack of GluR-B Containing AMPA Receptors But Not of NMDA Receptors in Hypothalamic and Septal Neurons

Author Correction: Voltage-independent GluN2A-type NMDA receptor Ca 2+ signaling promotes audiogenic seizures, attentional and cognitive deficits in mice

Voltage-independent GluN2A-type NMDA receptor Ca 2+ signaling promotes audiogenic seizures, attentional and cognitive deficits in mice

Developmental impact of a familial GABA A receptor epilepsy mutation

Developmental impact of a familial GABA sub(A) receptor epilepsy mutation

Mice with Genetically Modified NMDA and AMPA Receptors

Point mutation in an AMPA receptor gene lethality in mice deficient in the RNA-editing enzyme ADAR2

Functional knock down of VCAM1 in mice mediated by endoplasmatic reticulum retained intrabodies

Nickel decatungstate [Ni(C2H6SO)5(H2O)]2[W10O32]: Synthesis from a water-dimethylsulfoxide solution, crystal structure determination, IR and Raman spec-troscopic analysis, surface micromorphology

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