Literature DB >> 18923513

Failure of neuronal homeostasis results in common neuropsychiatric phenotypes.

Melissa B Ramocki1, Huda Y Zoghbi.   

Abstract

Failure of normal brain development leads to mental retardation or autism in about 3% of children. Many genes integral to pathways by which synaptic modification and the remodelling of neuronal networks mediate cognitive and social development have been identified, usually through loss of function. Evidence is accumulating, however, that either loss or gain of molecular functions can be deleterious to the nervous system. Copy-number variation, regulation of gene expression by non-coding RNAs and epigenetic changes are all mechanisms by which altered gene dosage can cause the failure of neuronal homeostasis.

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Year:  2008        PMID: 18923513      PMCID: PMC2696622          DOI: 10.1038/nature07457

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  69 in total

1.  MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number.

Authors:  Hsiao-Tuan Chao; Huda Y Zoghbi; Christian Rosenmund
Journal:  Neuron       Date:  2007-10-04       Impact factor: 17.173

2.  Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.

Authors:  Richard Paylor; Beate Glaser; Annalisa Mupo; Paris Ataliotis; Corinne Spencer; Angela Sobotka; Chelsey Sparks; Chul-Hee Choi; John Oghalai; Sarah Curran; Kieran C Murphy; Stephen Monks; Nigel Williams; Michael C O'Donovan; Michael J Owen; Peter J Scambler; Elizabeth Lindsay
Journal:  Proc Natl Acad Sci U S A       Date:  2006-05-09       Impact factor: 11.205

Review 3.  Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders.

Authors:  Jennifer A Lee; James R Lupski
Journal:  Neuron       Date:  2006-10-05       Impact factor: 17.173

Review 4.  Transcription, translation and fragile X syndrome.

Authors:  Kathryn Garber; Karen T Smith; Danny Reines; Stephen T Warren
Journal:  Curr Opin Genet Dev       Date:  2006-05-02       Impact factor: 5.578

Review 5.  MeCP2 dysfunction in Rett syndrome and related disorders.

Authors:  Paolo Moretti; Huda Y Zoghbi
Journal:  Curr Opin Genet Dev       Date:  2006-05-02       Impact factor: 5.578

6.  Phosphorylation of actin-depolymerizing factor/cofilin by LIM-kinase mediates amyloid beta-induced degeneration: a potential mechanism of neuronal dystrophy in Alzheimer's disease.

Authors:  Lorena Heredia; Pablo Helguera; Soledad de Olmos; Gabriela Kedikian; Francisco Solá Vigo; Frank LaFerla; Matthias Staufenbiel; José de Olmos; Jorge Busciglio; Alfredo Cáceres; Alfredo Lorenzo
Journal:  J Neurosci       Date:  2006-06-14       Impact factor: 6.167

Review 7.  Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes.

Authors:  Lisa J Kobrynski; Kathleen E Sullivan
Journal:  Lancet       Date:  2007-10-20       Impact factor: 79.321

8.  Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptors.

Authors:  Mika Nakamoto; Vijayalaxmi Nalavadi; Michael P Epstein; Usha Narayanan; Gary J Bassell; Stephen T Warren
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-19       Impact factor: 11.205

9.  Parkin interacts with LIM Kinase 1 and reduces its cofilin-phosphorylation activity via ubiquitination.

Authors:  Meng K Lim; Takeshi Kawamura; Yosuke Ohsawa; Masafumi Ohtsubo; Shuichi Asakawa; Atsushi Takayanagi; Nobuyoshi Shimizu
Journal:  Exp Cell Res       Date:  2007-04-20       Impact factor: 3.905

10.  Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.

Authors:  Jonathan S Berg; Nicola Brunetti-Pierri; Sarika U Peters; Sung-Hae L Kang; Chin-to Fong; Jessica Salamone; Debra Freedenberg; Vickie L Hannig; Lisa Albers Prock; David T Miller; Peter Raffalli; David J Harris; Robert P Erickson; Christopher Cunniff; Gary D Clark; Maria A Blazo; Daniel A Peiffer; Kevin L Gunderson; Trilochan Sahoo; Ankita Patel; James R Lupski; Arthur L Beaudet; Sau Wai Cheung
Journal:  Genet Med       Date:  2007-07       Impact factor: 8.822

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  192 in total

Review 1.  Networking in autism: leveraging genetic, biomarker and model system findings in the search for new treatments.

Authors:  Jeremy Veenstra-VanderWeele; Randy D Blakely
Journal:  Neuropsychopharmacology       Date:  2011-09-21       Impact factor: 7.853

2.  Activity-dependent regulation of inhibition via GAD67.

Authors:  C Geoffrey Lau; Venkatesh N Murthy
Journal:  J Neurosci       Date:  2012-06-20       Impact factor: 6.167

Review 3.  Excitatory/Inhibitory Balance and Circuit Homeostasis in Autism Spectrum Disorders.

Authors:  Sacha B Nelson; Vera Valakh
Journal:  Neuron       Date:  2015-08-19       Impact factor: 17.173

Review 4.  From the genetic architecture to synaptic plasticity in autism spectrum disorder.

Authors:  Thomas Bourgeron
Journal:  Nat Rev Neurosci       Date:  2015-09       Impact factor: 34.870

5.  Induced gamma oscillations differentiate familiar and novel voices in children with MECP2 duplication and Rett syndromes.

Authors:  Sarika U Peters; Reyna L Gordon; Alexandra P Key
Journal:  J Child Neurol       Date:  2014-04-27       Impact factor: 1.987

6.  TAR DNA-Binding Protein 43 and Disrupted in Schizophrenia 1 Coaggregation Disrupts Dendritic Local Translation and Mental Function in Frontotemporal Lobar Degeneration.

Authors:  Ryo Endo; Noriko Takashima; Yoko Nekooki-Machida; Yusuke Komi; Kelvin Kai-Wan Hui; Masaki Takao; Hiroyasu Akatsu; Shigeo Murayama; Akira Sawa; Motomasa Tanaka
Journal:  Biol Psychiatry       Date:  2018-03-29       Impact factor: 13.382

7.  Krüppel mediates the selective rebalancing of ion channel expression.

Authors:  Jay Z Parrish; Charles C Kim; Lamont Tang; Sharon Bergquist; Tingting Wang; Joseph L Derisi; Lily Yeh Jan; Yuh Nung Jan; Graeme W Davis
Journal:  Neuron       Date:  2014-05-07       Impact factor: 17.173

8.  Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.

Authors:  Wei-Hsiang Huang; Casey J Guenthner; Jin Xu; Tiffany Nguyen; Lindsay A Schwarz; Alex W Wilkinson; Or Gozani; Howard Y Chang; Mehrdad Shamloo; Liqun Luo
Journal:  Neuron       Date:  2016-09-29       Impact factor: 17.173

Review 9.  Age, plasticity, and homeostasis in childhood brain disorders.

Authors:  Maureen Dennis; Brenda J Spiegler; Jenifer J Juranek; Erin D Bigler; O Carter Snead; Jack M Fletcher
Journal:  Neurosci Biobehav Rev       Date:  2013-10-03       Impact factor: 8.989

10.  Control of cognition and adaptive behavior by the GLP/G9a epigenetic suppressor complex.

Authors:  Anne Schaefer; Srihari C Sampath; Adam Intrator; Alice Min; Tracy S Gertler; D James Surmeier; Alexander Tarakhovsky; Paul Greengard
Journal:  Neuron       Date:  2009-12-10       Impact factor: 17.173

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