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(361 - 380 of 398)

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A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51
Mutagenic consequences of a single G-quadruplex demonstrate mitotic inheritance of DNA replication fork barriers
The transcriptional landscape of age in human peripheral blood
Direct quantitative detection of Doc2b-induced hemifusion in optically trapped membranes
BMP signalling differentially regulates distinct haematopoietic stem cell types
Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome
De novo mutations in PLXND1 and REV3L cause Mobius syndrome
System-wide identification of wild-type SUMO-2 conjugation sites
Polymerase Theta is a key driver of genome evolution and of CRISPR/Cas9-mediated mutagenesis
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels
Crossreactivity to vinculin and microbes provides a molecular basis for HLA-based protection against rheumatoid arthritis
Large-scale recent expansion of European patrilineages shown by population resequencing
The interferon-related developmental regulator 1 is used by human papillomavirus to suppress NF kappa B activation
Glycosylation of immunoglobulin G determines osteoclast differentiation and bone loss
Brown fat activation reduces hypercholesterolaemia and protects from atherosclerosis development
Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels
Demonstration of asymmetric electron conduction in pseudosymmetrical photosynthetic reaction centre proteins in an electrical circuit
Beating beats mixing in heterodyne detection schemes
Non-plasmonic nanoantennas for surface enhanced spectroscopies with ultra-low heat conversion
DNA methylation signatures link prenatal famine exposure to growth and metabolism

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