Is mental retardation a defect of synapse structure and function? (Q35296262)

7 August 2017

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title

Is mental retardation a defect of synapse structure and function? (English)

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7 August 2017

Magdalena Chechlacz

1

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7 August 2017

Joseph G Gleeson

series ordinal

2

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7 August 2017

publication date

1 July 2003

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7 August 2017

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7 August 2017

volume

29

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7 August 2017

issue

1

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7 August 2017

page(s)

11-17

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How many X-linked genes for non-specific mental retardation (MRX) are there?

7 August 2017

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7 January 2021

Role of actin in anchoring postsynaptic receptors in cultured hippocampal neurons: differential attachment of NMDA versus AMPA receptors.

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7 January 2021

Differential regional expression and ultrastructural localization of alpha-actinin-2, a putative NMDA receptor-anchoring protein, in rat brain.

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7 January 2021

Making the connection: Cytoskeletal rearrangements during growth cone guidance

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7 January 2021

Neurabin: a novel neural tissue-specific actin filament-binding protein involved in neurite formation

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7 January 2021

Cytoskeletal dynamics in dendritic spines: direct modulation by glutamate receptors?

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7 January 2021

The Rho's progress: a potential role during neuritogenesis for the Rho family of GTPases

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7 January 2021

Rho family GTP-binding proteins in growth cone signalling

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7 January 2021

Rho GTPases in neuronal morphogenesis

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7 January 2021

Dynamic mechanisms of neuronal outgrowth.

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Cytoskeletal reorganization underlying growth cone motility

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Pioneer growth cone steering decisions mediated by single filopodial contacts in situ.

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7 January 2021

Alpha-actinins, calspectin (brain spectrin or fodrin), and actin participate in adhesion and movement of growth cones

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7 January 2021

Ephrin-A5 induces collapse of growth cones by activating Rho and Rho kinase

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7 January 2021

Rho GTPases in growth cone guidance

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7 January 2021

Regulation of neurotrophin-induced axonal responses via Rho GTPases

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7 January 2021

Rho proteins and the cellular mechanisms of mental retardation.

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7 January 2021

Rho family GTPases and neuronal growth cone remodelling: relationship between increased complexity induced by Cdc42Hs, Rac1, and acetylcholine and collapse induced by RhoA and lysophosphatidic acid

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7 January 2021

ChIPping away at potassium channel regulation

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7 January 2021

Rapid dendritic remodeling in the developing retina: dependence on neurotransmission and reciprocal regulation by Rac and Rho.

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7 January 2021

Rac1 and Cdc42 but not RhoA or Rho kinase activities are required for neurite outgrowth induced by the Netrin-1 receptor DCC (deleted in colorectal cancer) in N1E-115 neuroblastoma cells

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7 January 2021

Regulation of dendritic growth and remodeling by Rho, Rac, and Cdc42.

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7 January 2021

Actin dynamics in dendritic spines: a form of regulated plasticity at excitatory synapses

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7 January 2021

Contributions of dendritic spines and perforated synapses to synaptic plasticity

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7 January 2021

Postsynaptic actin and neuronal plasticity

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7 January 2021

Actin-based plasticity in dendritic spines

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7 January 2021

PAK3 mutation in nonsyndromic X-linked mental retardation

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7 January 2021

Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation.

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7 January 2021

Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardation

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7 January 2021

Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation

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7 January 2021

Dendritic development in neocortex of children with mental defect and infantile spasms

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7 January 2021

Dendritic Spine "Dysgenesis" and Mental Retardation

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7 January 2021

Pyramidal cell abnormalities in the motor cortex of a child with Down's syndrome. A Golgi study

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7 January 2021

Adult fragile X syndrome. Clinico-neuropathologic findings

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7 January 2021

Dendritic spine anomalies in fetal alcohol syndrome

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7 January 2021

Down's syndrome and Alzheimer's disease: dendritic spine counts in the hippocampus.

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7 January 2021

Analysis of neocortex in three males with the fragile X syndrome

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7 January 2021

Structural abnormalities of the cerebral cortex in human chromosomal aberrations: a Golgi study

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7 January 2021

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

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7 January 2021

Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.

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7 January 2021

Abnormal development of dendritic spines in FMR1 knock-out mice

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7 January 2021

Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor.

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7 January 2021

Mutations in GDI1 are responsible for X-linked non-specific mental retardation

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7 January 2021

The small GTP-binding protein Rab3A regulates a late step in synaptic vesicle fusion

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7 January 2021

Role of rab GDP dissociation inhibitor alpha in regulating plasticity of hippocampal neurotransmission

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7 January 2021

ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation

1 reference

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7 January 2021

FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900152-8

7 January 2021

Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island

1 reference

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7 January 2021

Identification of the gene FMR2, associated with FRAXE mental retardation

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7 January 2021

Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain.

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7 January 2021

A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation

1 reference

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7 January 2021

A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900152-8

7 January 2021

A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900152-8

7 January 2021

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900152-8

7 January 2021

Molecular-clinical spectrum of the ATR-X syndrome

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7 January 2021

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900152-8

7 January 2021

MECP2 is highly mutated in X-linked mental retardation

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https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900152-8

7 January 2021

Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome

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https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900152-8

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900152-8

7 January 2021

Morphologic and histoanatomic observations of the brain in untreated human phenylketonuria

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7 January 2021

10.1016/S0887-8994(03)00152-8

Identifiers

DOI

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7 August 2017

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