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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/oup/periodical/hmg/2010/volume_19
has manifestation of work	http://hub.abes.fr/oup/periodical/hmg/2010/volume_19/issue_23/m/print http://hub.abes.fr/oup/periodical/hmg/2010/volume_19/issue_23/m/web
Date Copyrighted	2010
Rights	© The Author 2010. Published by Oxford University Press. Published by Oxford University Press 2010 © The Author 2010. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org © The Author 2010. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com
issue	23
Access Rights	creative-commons
is Is Part Of of	Functional interactions between the LRP6 WNT co-receptor and folate supplementation Contents Page Editorial Board Removal of the calpain 3 protease reverses the myopathology in a mouse model for titinopathies Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese The distribution of repressive histone modifications on silenced FMR1 alleles provides clues to the mechanism of gene silencing in fragile X syndrome Discovery of the BMPR1A promoter and germline mutations that cause juvenile polyposis Genetic diversity at endoplasmic reticulum aminopeptidases is maintained by balancing selection and is associated with natural resistance to HIV-1 infection K14 mRNA reprogramming for dominant epidermolysis bullosa simplex Puromycin-sensitive aminopeptidase protects against aggregation-prone proteins via autophagy The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation Oligodendrocyte progenitor cell numbers and migration are regulated by the zebrafish orthologs of the NF1 tumor suppressor gene Sequestration of chaperones and proteasome into Lafora bodies and proteasomal dysfunction induced by Lafora disease-associated mutations of malin Subscription Page Mapping of numerous disease-associated expression polymorphisms in primary peripheral blood CD4+ lymphocytes Cone and rod photoreceptor transplantation in models of the childhood retinopathy Leber congenital amaurosis using flow-sorted Crx-positive donor cells Functional relevance of the IRF-1 promoter polymorphism rs2549009 on transcriptional activity in a native genomic environment An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD) Shox2 mediates Tbx5 activity by regulating Bmp4 in the pacemaker region of the developing heart HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones Cover Page De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy

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