De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
Genetic ancestry and monogenic disease risk in the Scottish Traveller founder population.
WONOEP appraisal: Biomarkers and treatment strategies beyond the synapse
Small RNA sequencing identifies serum tDR-1:34-Gly-GCC tiRNA levels as a biomarker for survival in amyotrophic lateral sclerosis
The landscape of hereditary haemochromatosis risk and diagnosis across the British Isles and Ireland
Distinct Argonaute2-associated small RNA profiles in microglia and neurons drive cell-specific responses in a mouse model of temporal lobe epilepsy
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
EHD4 and ASAP2 are critical negative regulators of the claudin-5-based endothelial barrier
Temporal Dynamics of tsRNA Regulation Mark an Abrupt Transition After Epileptogenesis
Altered Short Non-Coding RNA Landscape in the Hippocampus of a Mouse Model of CDKL5 Deficiency Disorder
Genome-wide gene-environment interaction study uncovers 162 vitamin D status variants using a precise ambient UVB measure
Serum small non-coding RNA define molecular subtypes in amyotrophic lateral sclerosis
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