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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/oup/periodical/hmg/2009/volume_18
has manifestation of work	http://hub.abes.fr/oup/periodical/hmg/2009/volume_18/issue_4/m/print http://hub.abes.fr/oup/periodical/hmg/2009/volume_18/issue_4/m/web
Date Copyrighted	2009
Rights	© The Author 2009. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org © The Author 2008. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org © 2008 The Author(s)
issue	4
Access Rights	creative-commons
is Is Part Of of	Altered serotonin receptor expression is associated with depression-related behavior in the R6/1 transgenic mouse model of Huntington's disease Subscription Page Contents Page Differential nuclear scaffold/matrix attachment marks expressed genes Unbalanced deoxynucleotide pools cause mitochondrial DNA instability in thymidine phosphorylase-deficient mice Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Interactions between the juvenile Batten disease gene, CLN3, and the Notch and JNK signalling pathways Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation Zebrafish Tsc1 reveals functional interactions between the cilium and the TOR pathway Cardiac-specific ablation of Cypher leads to a severe form of dilated cardiomyopathy with premature death Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice Editorial Board The malin-laforin complex suppresses the cellular toxicity of misfolded proteins by promoting their degradation through the ubiquitin-proteasome system Cover Page Severe neurological phenotypes of Q129 DRPLA transgenic mice serendipitously created by en masse expansion of CAG repeats in Q76 DRPLA mice Targeted resequencing of two genes, RAGE and POLL, confirms findings from a genome-wide scan for adaptive evolution and provides evidence for positive selection in additional populations Positive and negative feedback regulates the transcription factor FOXL2 in response to cell stress: evidence for a regulatory imbalance induced by disease-causing mutations GRM7 variants confer susceptibility to age-related hearing impairment Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy Effects of overexpression of Huntingtin proteins on mitochondrial integrity

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