Literature DB >> 21971015

Behavioural and cognitive profiles of mouse models for Prader-Willi syndrome.

Dinko Relkovic1, Anthony R Isles.   

Abstract

Prader-Willi syndrome (PWS) is a neurodevelopmental disorder with aspects of psychiatric illness caused by genetic mutations at chromosome 15q11-q13. In addition to causing PWS, this interval is also thought to be of importance more generally in the development of autism and psychotic illness. The PWS genetic interval is conserved in mammals, and consequently mice carrying genetic manipulations affecting one or all of the genes in the region of conserved synteny have been generated and used in neurobehavioural studies. Here we give an overview of these models and describe the behavioural and neurobiological analyses that have been performed, many of which have provide new insights into the molecular and neural processes influenced by genes within the PWS interval.
Copyright © 2011 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 21971015     DOI: 10.1016/j.brainresbull.2011.09.009

Source DB:  PubMed          Journal:  Brain Res Bull        ISSN: 0361-9230            Impact factor:   4.077


  9 in total

1.  Adult-onset deletion of the Prader-Willi syndrome susceptibility gene Snord116 in mice results in reduced feeding and increased fat mass.

Authors:  Louise Purtell; Yue Qi; Lesley Campbell; Amanda Sainsbury; Herbert Herzog
Journal:  Transl Pediatr       Date:  2017-04

2.  An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in mice.

Authors:  Mei-Yi Wu; Ming Jiang; Xiaodong Zhai; Arthur L Beaudet; Ray-Chang Wu
Journal:  PLoS One       Date:  2012-04-04       Impact factor: 3.240

Review 3.  Genomic Imprinting.

Authors:  Emirjeta Bajrami; Mirko Spiroski
Journal:  Open Access Maced J Med Sci       Date:  2016-02-04

4.  Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome.

Authors:  Jennifer R Davies; Trevor Humby; Dominic M Dwyer; Alastair S Garfield; Hannah Furby; Lawrence S Wilkinson; Timothy Wells; Anthony R Isles
Journal:  Eur J Neurosci       Date:  2015-06-25       Impact factor: 3.386

Review 5.  Epigenetics in Prader-Willi Syndrome.

Authors:  Aron Judd P Mendiola; Janine M LaSalle
Journal:  Front Genet       Date:  2021-02-15       Impact factor: 4.599

6.  Learning by observation and learning by doing in Prader-Willi syndrome.

Authors:  Francesca Foti; Deny Menghini; Enzo Orlandi; Cristina Rufini; Antonino Crinò; Sabrina Spera; Stefano Vicari; Laura Petrosini; Laura Mandolesi
Journal:  J Neurodev Disord       Date:  2015-02-26       Impact factor: 4.025

7.  Maternal transcription of non-protein coding RNAs from the PWS-critical region rescues growth retardation in mice.

Authors:  Timofey S Rozhdestvensky; Thomas Robeck; Chenna R Galiveti; Carsten A Raabe; Birte Seeger; Anna Wolters; Leonid V Gubar; Jürgen Brosius; Boris V Skryabin
Journal:  Sci Rep       Date:  2016-02-05       Impact factor: 4.379

8.  Longitudinal Effects of Developmental Bisphenol A Exposure on Epigenome-Wide DNA Hydroxymethylation at Imprinted Loci in Mouse Blood.

Authors:  Joseph J Kochmanski; Elizabeth H Marchlewicz; Raymond G Cavalcante; Bambarendage P U Perera; Maureen A Sartor; Dana C Dolinoy
Journal:  Environ Health Perspect       Date:  2018-07-23       Impact factor: 9.031

9.  Functional diversity of small nucleolar RNAs.

Authors:  Tomaž Bratkovič; Janja Božič; Boris Rogelj
Journal:  Nucleic Acids Res       Date:  2020-02-28       Impact factor: 16.971

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.