Literature DB >> 15286155

Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissues.

K Nakabayashi, S Makino, S Minagawa, A C Smith, J S Bamforth, P Stanier, M Preece, L Parker-Katiraee, T Paton, M Oshimura, P Mill, Y Yoshikawa, C C Hui, D Monk, G E Moore, S W Scherer.   

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Year:  2004        PMID： 15286155      PMCID： PMC1735868          DOI： 10.1136/jmg.2003.014142

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  20 in total

Review 1.  The role of imprinted genes in fetal growth abnormalities.

Authors:  Jorge A Piedrahita
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2011-06-06

Review 2.  The origin and evolution of genomic imprinting and viviparity in mammals.

Authors:  Marilyn B Renfree; Shunsuke Suzuki; Tomoko Kaneko-Ishino
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2013-01-05       Impact factor: 6.237

3.  Transcriptional changes in Huntington disease identified using genome-wide expression profiling and cross-platform analysis.

Authors:  Kristina Becanovic; Mahmoud A Pouladi; Raymond S Lim; Alexandre Kuhn; Paul Pavlidis; Ruth Luthi-Carter; Michael R Hayden; Blair R Leavitt
Journal:  Hum Mol Genet       Date:  2010-01-20       Impact factor: 6.150

4.  Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues.

Authors:  Layla Parker-Katiraee; Eleni Bousiaki; David Monk; Gudrun E Moore; Kazuhiko Nakabayashi; Stephen W Scherer
Journal:  Hum Mol Genet       Date:  2008-08-04       Impact factor: 6.150

5.  Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing.

Authors:  David Monk; Alexandre Wagschal; Philippe Arnaud; Pari-Sima Müller; Layla Parker-Katiraee; Déborah Bourc'his; Stephen W Scherer; Robert Feil; Philip Stanier; Gudrun E Moore
Journal:  Genome Res       Date:  2008-05-14       Impact factor: 9.043

6.  Deregulation of an imprinted gene network in prostate cancer.

Authors:  Teodora Ribarska; Wolfgang Goering; Johanna Droop; Klaus-Marius Bastian; Marc Ingenwerth; Wolfgang A Schulz
Journal:  Epigenetics       Date:  2014-02-10       Impact factor: 4.528

7.  Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene.

Authors:  C Bonnet; M-J Grégoire; M Vibert; E Raffo; B Leheup; P Jonveaux
Journal:  J Hum Genet       Date:  2008-07-24       Impact factor: 3.172

8.  Detection of recurrent rearrangement breakpoints from copy number data.

Authors:  Anna Ritz; Pamela L Paris; Michael M Ittmann; Colin Collins; Benjamin J Raphael
Journal:  BMC Bioinformatics       Date:  2011-04-21       Impact factor: 3.169

9.  Detection of Parent-of-Origin Effects for the Variants Associated With Behavioral Disinhibition in the MCTFR Data.

Authors:  Yi-Fan Kong; Meng-Kai Li; Yu-Xin Yuan; Zi-Ying Yang; Wen-Yi Yu; Pei-Zhen Zhao; Ji-Yuan Zhou
Journal:  Front Genet       Date:  2022-04-26       Impact factor: 4.772

10.  Identification of quantitative trait loci (QTL) for canine hip dysplasia and canine elbow dysplasia in Bernese mountain dogs.

Authors:  Sophia Pfahler; Ottmar Distl
Journal:  PLoS One       Date:  2012-11-26       Impact factor: 3.240
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