Literature DB >> 11407158

Developmental disorders of activity dependent neuronal plasticity.

M V Johnston1.   

Abstract

A number of neurodevelopmental disorders are caused by defects in activity dependent neuronal plasticity, the process by which neuronal activity shapes developing neuronal circuits. These disorders are caused by genetic mutations or other factors that disrupt intracellular signaling pathways that link the cell surface with the nuclear machinery for gene expression. The signaling pathways disrupted by these disorders are involved in learning, memory and behavior as well as in the synaptic proliferation and pruning that occurs during normal development. Examples of neurodevelopmental disorders that target plasticity include X-linked disorders such as Rett, Fragile-X and Coffin-Lowry Syndromes as well as acquired disorders such as cretinism. Several other X-linked mental retardation syndromes as well as autosomal disorders including neurofibromatosis type 1 and tuberous sclerosis also involve signaling pathways involved in neuronal plasticity. Disruption of neuronal plasticity is a mechanism that may underlie a diverse group of neurodevelopmental disorders.

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Year:  2001        PMID: 11407158     DOI: 10.1007/bf02723021

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  20 in total

Review 1.  Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation.

Authors:  J Chelly
Journal:  Hum Mol Genet       Date:  1999       Impact factor: 6.150

2.  Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes.

Authors:  Y Feng; C A Gutekunst; D E Eberhart; H Yi; S T Warren; S M Hersch
Journal:  J Neurosci       Date:  1997-03-01       Impact factor: 6.167

Review 3.  Rett syndrome: a disorder affecting early brain growth.

Authors:  S Naidu
Journal:  Ann Neurol       Date:  1997-07       Impact factor: 10.422

4.  Cognitive impairment in Coffin-Lowry syndrome correlates with reduced RSK2 activation.

Authors:  K H Harum; L Alemi; M V Johnston
Journal:  Neurology       Date:  2001-01-23       Impact factor: 9.910

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

Authors:  R E Amir; I B Van den Veyver; M Wan; C Q Tran; U Francke; H Y Zoghbi
Journal:  Nat Genet       Date:  1999-10       Impact factor: 38.330

Review 6.  Brain waves and brain wiring: the role of endogenous and sensory-driven neural activity in development.

Authors:  A A Penn; C J Shatz
Journal:  Pediatr Res       Date:  1999-04       Impact factor: 3.756

7.  Synaptic synthesis of the Fragile X protein: possible involvement in synapse maturation and elimination.

Authors:  I J Weiler; W T Greenough
Journal:  Am J Med Genet       Date:  1999-04-02

8.  A mouse model for the learning and memory deficits associated with neurofibromatosis type I.

Authors:  A J Silva; P W Frankland; Z Marowitz; E Friedman; G S Laszlo; D Cioffi; T Jacks; R Bourtchuladze; G Lazlo
Journal:  Nat Genet       Date:  1997-03       Impact factor: 38.330

9.  PAK3 mutation in nonsyndromic X-linked mental retardation.

Authors:  K M Allen; J G Gleeson; S Bagrodia; M W Partington; J C MacMillan; R A Cerione; J C Mulley; C A Walsh
Journal:  Nat Genet       Date:  1998-09       Impact factor: 38.330

10.  Signaling from synapse to nucleus: postsynaptic CREB phosphorylation during multiple forms of hippocampal synaptic plasticity.

Authors:  K Deisseroth; H Bito; R W Tsien
Journal:  Neuron       Date:  1996-01       Impact factor: 17.173

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  4 in total

1.  Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome.

Authors:  Shelli R Kesler; Christine M Blasey; Wendy E Brown; Jerome Yankowitz; She Min Zeng; Bruce G Bender; Allan L Reiss
Journal:  Biol Psychiatry       Date:  2003-09-15       Impact factor: 13.382

Review 2.  Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.

Authors:  Anna Järvinen-Pasley; Ursula Bellugi; Judy Reilly; Debra L Mills; Albert Galaburda; Allan L Reiss; Julie R Korenberg
Journal:  Dev Psychopathol       Date:  2008

3.  Anaplerotic triheptanoin diet enhances mitochondrial substrate use to remodel the metabolome and improve lifespan, motor function, and sociability in MeCP2-null mice.

Authors:  Min Jung Park; Susan Aja; Qun Li; Alicia L Degano; Judith Penati; Justin Zhuo; Charles R Roe; Gabriele V Ronnett
Journal:  PLoS One       Date:  2014-10-09       Impact factor: 3.240

Review 4.  Oxytocin and Oxytocin Receptor Gene Regulation in Williams Syndrome: A Systematic Review.

Authors:  Elif Çalışkan; Munise Nur Şahin; Mahmut Alper Güldağ
Journal:  Yale J Biol Med       Date:  2021-12-29
  4 in total

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