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Selective alteration of adult hippocampal neurogenesis and impaired spatial pattern separation performance in the RSK2-deficient mouse model of Coffin-Lowry syndrome

Neurobiology of disease, 2018-07, Vol.115, p.69-81

2018

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Coffin-Lowry syndrome

European journal of human genetics : EJHG, 2010-06, Vol.18 (6), p.627-633

2010

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The Coffin-Lowry syndrome-associated protein RSK2 regulates neurite outgrowth through phosphorylation of phospholipase D1 (PLD1) and synthesis of phosphatidic acid

The Journal of neuroscience, 2013-12, Vol.33 (50), p.19470-19479

2013

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PLD1 participates in BDNF-induced signalling in cortical neurons

Scientific reports, 2015-10, Vol.5 (1), p.14778-14778, Article 14778

2015

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Structural and Functional Basis for p38-MK2-Activated Rsk Signaling in Toll-Like Receptor-Stimulated Dendritic Cells

Molecular and cellular biology, 2015-01, Vol.35 (1), p.132-140

2015

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Requirement of Rsk-2 for Epidermal Growth Factor-Activated Phosphorylation of Histone H3

Science (American Association for the Advancement of Science), 1999-08, Vol.285 (5429), p.886-891

1999

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The PDK1-Rsk Signaling Pathway Controls Langerhans Cell Proliferation and Patterning

The Journal of immunology (1950), 2015-11, Vol.195 (9), p.4264-4272

2015

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RSK2 is a modulator of craniofacial development

PloS one, 2014-01, Vol.9 (1), p.e84343-e84343

2014

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Fibroblast Growth Factor Receptor 3 Associates with and Tyrosine Phosphorylates p90 RSK2, Leading to RSK2 Activation That Mediates Hematopoietic Transformation

Molecular and Cellular Biology, 2009-04, Vol.29 (8), p.2105-2117

2009

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Defective synaptic transmission and structure in the dentate gyrus and selective fear memory impairment in the Rsk2 mutant mouse model of Coffin–Lowry syndrome

Neurobiology of disease, 2013-10, Vol.58 (58), p.156-168

2013

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Rsk2 Knockdown in PC12 Cells Results in Sp1 Dependent Increased Expression of the Gria2 Gene, Encoding the AMPA Receptor Subunit GluR2

International journal of molecular sciences, 2013-02, Vol.14 (2), p.3358-3375

2013

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Rsk-2 Activity is Necessary for Epidermal Growth Factor-Induced Phosphorylation of CREB Protein and Transcription of C-fos Gene

Proceedings of the National Academy of Sciences - PNAS, 1998-10, Vol.95 (21), p.12202-12207

1998

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p90Rsk is not involved in cytostatic factor arrest in mouse oocytes

The Journal of cell biology, 2005-04, Vol.169 (2), p.227-231

2005

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Expression analysis of RSK gene family members: the RSK2 gene, mutated in Coffin–Lowry syndrome, is prominently expressed in brain structures essential for cognitive function and learning

Human molecular genetics, 2002-11, Vol.11 (23), p.2929-2940

2002

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Coffin-Lowry syndrome-associated protein RSK2 is implicated in calcium-regulated exocytosis through the regulation of PLD1

Proceedings of the National Academy of Sciences - PNAS, 2008-06, Vol.105 (24), p.8434-8439

2008

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RSK2 Signaling in Medial Habenula Contributes to Acute Morphine Analgesia

Neuropsychopharmacology (New York, N.Y.), 2012-04, Vol.37 (5), p.1288-1296

2012

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Stimulus-induced drop episodes in Coffin–Lowry syndrome

European journal of medical genetics, 2012-05, Vol.55 (5), p.335-337

2012

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Inactivation of the CDKL3 gene at 5q31.1 by a balanced t(X;5) translocation associated with nonspecific mild mental retardation

American journal of medical genetics. Part A, 2008-05, Vol.146A (10), p.1267-1279

2008

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RSK2 Signaling in Brain Habenula Contributes to Place Aversion Learning

Learning & memory (Cold Spring Harbor, N.Y.), 2011-09, Vol.18 (9), p.574-578

2011

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Dopaminergic system dysregulation in the mrsk2_KO mouse, an animal model of the Coffin-Lowry syndrome

Journal of neurochemistry, 2008-12, Vol.107 (5), p.1325-1334

2008

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Altered ERK/MAPK signaling in the hippocampus of the mrsk2_KO mouse model of Coffin‐Lowry syndrome

Journal of neurochemistry, 2011-11, Vol.119 (3), p.447-459

2011

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Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin-Lowry syndrome

Human genetics, 2011-03, Vol.129 (3), p.255-269

2011

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The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patient

Human genetics, 2007-12, Vol.122 (5), p.541-543

2007

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Identification of the first deep intronic mutation in the RPS6KA3 gene in a patient with a severe form of Coffin–Lowry syndrome

European journal of medical genetics, 2013-03, Vol.56 (3), p.150-152

2013

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A missense mutation in RPS6KA3 ( RSK2 ) responsible for non-specific mental retardation

Nature genetics, 1999-05, Vol.22 (1), p.13-14

1999

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Selective alteration of adult hippocampal neurogenesis and impaired spatial pattern separation performance in the RSK2-deficient mouse model of Coffin-Lowry syndrome

Coffin-Lowry syndrome

The Coffin-Lowry syndrome-associated protein RSK2 regulates neurite outgrowth through phosphorylation of phospholipase D1 (PLD1) and synthesis of phosphatidic acid

PLD1 participates in BDNF-induced signalling in cortical neurons

Structural and Functional Basis for p38-MK2-Activated Rsk Signaling in Toll-Like Receptor-Stimulated Dendritic Cells

Requirement of Rsk-2 for Epidermal Growth Factor-Activated Phosphorylation of Histone H3

The PDK1-Rsk Signaling Pathway Controls Langerhans Cell Proliferation and Patterning

RSK2 is a modulator of craniofacial development

Fibroblast Growth Factor Receptor 3 Associates with and Tyrosine Phosphorylates p90 RSK2, Leading to RSK2 Activation That Mediates Hematopoietic Transformation

Defective synaptic transmission and structure in the dentate gyrus and selective fear memory impairment in the Rsk2 mutant mouse model of Coffin–Lowry syndrome

Rsk2 Knockdown in PC12 Cells Results in Sp1 Dependent Increased Expression of the Gria2 Gene, Encoding the AMPA Receptor Subunit GluR2

Rsk-2 Activity is Necessary for Epidermal Growth Factor-Induced Phosphorylation of CREB Protein and Transcription of C-fos Gene

p90Rsk is not involved in cytostatic factor arrest in mouse oocytes

Expression analysis of RSK gene family members: the RSK2 gene, mutated in Coffin–Lowry syndrome, is prominently expressed in brain structures essential for cognitive function and learning

Coffin-Lowry syndrome-associated protein RSK2 is implicated in calcium-regulated exocytosis through the regulation of PLD1

RSK2 Signaling in Medial Habenula Contributes to Acute Morphine Analgesia

Stimulus-induced drop episodes in Coffin–Lowry syndrome

Inactivation of the CDKL3 gene at 5q31.1 by a balanced t(X;5) translocation associated with nonspecific mild mental retardation

RSK2 Signaling in Brain Habenula Contributes to Place Aversion Learning

Dopaminergic system dysregulation in the mrsk2_KO mouse, an animal model of the Coffin-Lowry syndrome

Altered ERK/MAPK signaling in the hippocampus of the mrsk2_KO mouse model of Coffin‐Lowry syndrome

Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin-Lowry syndrome

The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patient

Identification of the first deep intronic mutation in the RPS6KA3 gene in a patient with a severe form of Coffin–Lowry syndrome

A missense mutation in RPS6KA3 ( RSK2 ) responsible for non-specific mental retardation

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