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Volume 23, Issue 3, 1 February 2014
Articles
The coiled-coil domain containing protein CCDC151 is required for the function of IFT-dependent motile cilia in animals
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 563–577, https://doi.org/10.1093/hmg/ddt445
Human chromosome 21 orthologous region on mouse chromosome 17 is a major determinant of Down syndrome-related developmental cognitive deficits
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 578–589, https://doi.org/10.1093/hmg/ddt446
Frequent and sex-biased deletion of SLX4IP by illegitimate V(D)J-mediated recombination in childhood acute lymphoblastic leukemia
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 590–601, https://doi.org/10.1093/hmg/ddt447
Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 602–617, https://doi.org/10.1093/hmg/ddt448
Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 618–636, https://doi.org/10.1093/hmg/ddt449
Rapamycin drives selection against a pathogenic heteroplasmic mitochondrial DNA mutation
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 637–647, https://doi.org/10.1093/hmg/ddt450
Altered CpG methylation in sporadic Alzheimer's disease is associated with APP and MAPT dysregulation
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 648–656, https://doi.org/10.1093/hmg/ddt451
Dynamic changes in DNA methylation and hydroxymethylation when hES cells undergo differentiation toward a neuronal lineage
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 657–667, https://doi.org/10.1093/hmg/ddt453
Widespread spinal cord transduction by intrathecal injection of rAAV delivers efficacious RNAi therapy for amyotrophic lateral sclerosis
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 668–681, https://doi.org/10.1093/hmg/ddt454
Abnormal Ras signaling in Costello syndrome (CS) negatively regulates enamel formation
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 682–692, https://doi.org/10.1093/hmg/ddt455
Tsc1 deficiency-mediated mTOR hyperactivation in vascular endothelial cells causes angiogenesis defects and embryonic lethality
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 693–705, https://doi.org/10.1093/hmg/ddt456
NLRP7 affects trophoblast lineage differentiation, binds to overexpressed YY1 and alters CpG methylation
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 706–716, https://doi.org/10.1093/hmg/ddt457
p53 increases caspase-6 expression and activation in muscle tissue expressing mutant huntingtin
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 717–729, https://doi.org/10.1093/hmg/ddt458
Reversibility of neuropathology in Tay–Sachs-related diseases
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 730–748, https://doi.org/10.1093/hmg/ddt459
Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 749–754, https://doi.org/10.1093/hmg/ddt460
DJ-1 modulates aggregation and pathogenesis in models of Huntington's disease
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 755–766, https://doi.org/10.1093/hmg/ddt466
Overexpression of synphilin-1 promotes clearance of soluble and misfolded alpha-synuclein without restoring the motor phenotype in aged A30P transgenic mice
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 767–781, https://doi.org/10.1093/hmg/ddt467
ASSOCIATION STUDIES ARTICLES
Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 782–795, https://doi.org/10.1093/hmg/ddt461
Genome-wide association study of ancestry-specific TB risk in the South African Coloured population
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 796–809, https://doi.org/10.1093/hmg/ddt462
Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 810–819, https://doi.org/10.1093/hmg/ddt463
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 820–830, https://doi.org/10.1093/hmg/ddt464
Genetic comorbidities in Parkinson's disease
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Pages 831–841, https://doi.org/10.1093/hmg/ddt465
FRONT-MATTER/BACK-MATTER
Contents Page
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Page NP, https://doi.org/10.1093/hmg/ddu015
Cover Page
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Page NP, https://doi.org/10.1093/hmg/ddu016
Editorial Board
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Page NP, https://doi.org/10.1093/hmg/ddu017
Subscription Page
Human Molecular Genetics, Volume 23, Issue 3, 1 February 2014, Page NP, https://doi.org/10.1093/hmg/ddu018
