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Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder
Oxford University Press | 2016| -
Nucleolar stress and impaired stress granule formation contribute to C9orf72 RAN translation-induced cytotoxicity
Oxford University Press | 2015| -
Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome
Oxford University Press | 2015| -
Characterization of the dipeptide repeat protein in the molecular pathogenesis of c9FTD/ALS
Oxford University Press | 2015| -
Epigenetics meets metabolomics: an epigenome-wide association study with blood serum metabolic traits
Oxford University Press | 2014| -
A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development
Oxford University Press | 2016| -
HDAC4: a key factor underlying brain developmental alterations in CDKL5 disorder
Oxford University Press | 2016| -
LncRNA-HOST2 regulates cell biological behaviors in epithelial ovarian cancer through a mechanism involving microRNA let-7b
Oxford University Press | 2015| -
Shorter telomere length in Europeans than in Africans due to polygenetic adaptation
Oxford University Press | 2016| -
Reduction of TMEM97 increases NPC1 protein levels and restores cholesterol trafficking in Niemann-pick type C1 disease cells
Oxford University Press | 2016| -
Restoration of muscle strength in dystrophic muscle by angiotensin-1-7 through inhibition of TGF-{beta} signalling
Oxford University Press | 2014| -
Preferential PPAR-{alpha} activation reduces neuroinflammation, and blocks neurodegeneration in vivo
Oxford University Press | 2016| -
A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis
Oxford University Press | 2016| -
Poly-dipeptides encoded by the C9ORF72 repeats block global protein translation
Oxford University Press | 2016| -
TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function
Oxford University Press | 2016| -
The Werner syndrome RECQ helicase targets G4 DNA in human cells to modulate transcription
Oxford University Press | 2016|