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Pubblicazioni
NATURE GENETICS
Rivista
Codice:
E116310
ISSN:
1061-4036
Dati Generali
Dati Generali
Pubblicazioni (21)
Pulisci
Ordina Pubblicazioni:
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Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database
Articolo
BCR-ABL suppresses C/EBP alpha expression through inhibitory action of hnRNP E2
Articolo
BMP signaling controls muscle mass
Articolo
BMP-6 is a Key Endogenous Regulator of Hepcidin Expression and Iron Metabolism
Articolo
Common variants in P2RY11 are associated with narcolepsy
Articolo
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
Articolo
Durum wheat genome highlights past domestication signatures and future improvement targets
Articolo
Erratum: Common variants in P2RY11 are associated with narcolepsy (Nature Genetics (2011) 43 (66-71))
Articolo
Erratum: Narcolepsy is strongly associated with the T-cell receptor alpha locus (Nature Genetics (2009) 41 (708-711))
Articolo
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
Articolo
Genome-wide association study identifies susceptibility loci for IgA nephropathy
Articolo
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis
Articolo
Identification of multiple independent susceptibility loci in the HLA region in Behçet's disease
Articolo
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy
Articolo
Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum
Articolo
Narcolepsy is strongly associated with the T-cell receptor alpha locus
Articolo
Natural variation in a homolog of Antirrhinum CENTRORADIALIS contributed to spring growth habit and environmental adaptation in cultivated barley
Articolo
Ocular Albinism: evidence for a defect in an intracellular signal transduction system.
Articolo
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Articolo
Single-cell multi-omics identifies chronic inflammation as a driver of TP53-mutant leukemic evolution
Articolo
The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability
Articolo
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