Literature DB >> 9287207

Genomic imprinting in the brain.

E B Keverne1.   

Abstract

Human genetic studies have directed attention to genetic imprinting in a number of syndromes involving brain dysfunction, such as Prader-Willi syndrome, Angelman syndrome, Turner's syndrome, bipolar depression and schizophrenia. Molecular genetics is providing insights into the complexity of these imprinting mechanisms, while experimental studies are revealing the differential roles that maternal and paternal genomes may play in brain development and growth.

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Year:  1997        PMID: 9287207     DOI: 10.1016/s0959-4388(97)80023-2

Source DB:  PubMed          Journal:  Curr Opin Neurobiol        ISSN: 0959-4388            Impact factor:   6.627


  15 in total

Review 1.  The impact of genomic imprinting for neurobehavioral and developmental disorders.

Authors:  R D Nicholls
Journal:  J Clin Invest       Date:  2000-02       Impact factor: 14.808

2.  A possible role for imprinted genes in inbreeding avoidance and dispersal from the natal area in mice.

Authors:  Anthony R Isles; Michael J Baum; Dan Ma; Abigail Szeto; Eric B Keverne; Nicholas D Allen
Journal:  Proc Biol Sci       Date:  2002-04-07       Impact factor: 5.349

3.  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 4.  Brain-expressed imprinted genes and adult behaviour: the example of Nesp and Grb10.

Authors:  Claire L Dent; Anthony R Isles
Journal:  Mamm Genome       Date:  2013-08-24       Impact factor: 2.957

5.  Methods of epigenome editing for probing the function of genomic imprinting.

Authors:  Kira DA Rienecker; Matthew J Hill; Anthony R Isles
Journal:  Epigenomics       Date:  2016-09-14       Impact factor: 4.778

6.  Further evidence of a maternal parent-of-origin effect on chromosome 10 in late-onset Alzheimer's disease.

Authors:  Susan Spear Bassett; Dimitrios Avramopoulos; Rodney T Perry; Howard Wiener; Bracie Watson; Rodney C P Go; M Daniele Fallin
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2006-07-05       Impact factor: 3.568

7.  Amygdala and hippocampal volumes in Turner syndrome: a high-resolution MRI study of X-monosomy.

Authors:  Shelli R Kesler; Amy Garrett; Bruce Bender; Jerome Yankowitz; She Min Zeng; Allan L Reiss
Journal:  Neuropsychologia       Date:  2004       Impact factor: 3.139

8.  Associations between parental broader autism phenotype and child autism spectrum disorder phenotype in the Study to Explore Early Development.

Authors:  Eric Rubenstein; Lisa D Wiggins; Laura A Schieve; Chyrise Bradley; Carolyn DiGuiseppi; Eric Moody; Juhi Pandey; Rebecca Edmondson Pretzel; Annie Green Howard; Andrew F Olshan; Brian W Pence; Julie Daniels
Journal:  Autism       Date:  2018-01-29

9.  Analysis of imprinting in mice with uniparental duplication of proximal chromosomes 7 and 15 by use of a custom oligonucleotide microarray.

Authors:  Victoria L Buettner; Jeffrey A Longmate; Michael E Barish; Jeffrey R Mann; Judith Singer-Sam
Journal:  Mamm Genome       Date:  2004-03       Impact factor: 2.957

Review 10.  Epigenetic factors and autism spectrum disorders.

Authors:  Bess M Flashner; Mark E Russo; Jenine E Boileau; Derek W Leong; G Ian Gallicano
Journal:  Neuromolecular Med       Date:  2013-03-07       Impact factor: 3.843

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