| human | Q5 |
| P8446 | Gateway to Research person ID | 07E525B2-A5AC-4C66-9DB8-AEF5E562185C |
| P856 | official website | https://pure.qub.ac.uk/en/persons/david-simpson |
| P496 | ORCID iD | 0000-0003-0157-1211 |
| P1153 | Scopus author ID | 7402412573 |
| P27 | country of citizenship | United Kingdom | Q145 |
| P108 | employer | Queen's University Belfast | Q877925 |
| P734 | family name | Simpson | Q2800825 |
| Simpson | Q2800825 | ||
| Simpson | Q2800825 | ||
| P101 | field of work | microRNA | Q310899 |
| vascular disease | Q1266890 | ||
| eye disease | Q3041498 | ||
| P735 | given name | David | Q18057751 |
| David | Q18057751 | ||
| P106 | occupation | researcher | Q1650915 |
| molecular biologist | Q15839206 | ||
| P21 | sex or gender | male | Q6581097 |
| Q100510780 | A Multi-Omics Approach Identifies Key Regulatory Pathways Induced by Long-Term Zinc Supplementation in Human Primary Retinal Pigment Epithelium |
| Q64915613 | A comparison of RNA extraction and sequencing protocols for detection of small RNAs in plasma. |
| Q40477757 | Characterisation of the advanced glycation endproduct receptor complex in the retinal pigment epithelium |
| Q38725922 | Considerations for optimization of microRNA PCR assays for molecular diagnosis. |
| Q34148754 | Deep sequencing reveals predominant expression of miR-21 amongst the small non-coding RNAs in retinal microvascular endothelial cells. |
| Q84509184 | Development of a diagnostic genetic test for simplex and autosomal recessive retinitis pigmentosa |
| Q37000197 | Diabetes downregulates large-conductance Ca2+-activated potassium beta 1 channel subunit in retinal arteriolar smooth muscle |
| Q92266624 | Differential Expression of Urinary Exosomal MicroRNAs miR-21-5p and miR-30b-5p in Individuals with Diabetic Kidney Disease |
| Q31120462 | Distinctive profile of IsomiR expression and novel microRNAs in rat heart left ventricle |
| Q42906347 | Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus |
| Q43495535 | Ex vivo expansion of human outgrowth endothelial cells leads to IL-8-mediated replicative senescence and impaired vasoreparative function. |
| Q30683767 | Expression of the 67 kDa laminin receptor (67LR) during retinal development: correlations with angiogenesis. |
| Q78171846 | Expression of the VEGF gene family during retinal vaso-obliteration and hypoxia |
| Q93921697 | Expression of vascular endothelial growth factor (VEGF) and its receptors is regulated in eyes with intra-ocular tumours |
| Q39625442 | Individual mRNA expression profiles reveal the effects of specific microRNAs. |
| Q95615097 | Kinematics and timing of Tertiary extension in the western Lake Mead region, Nevada |
| Q95615093 | Kinematics and timing of Tertiary extension in the western Lake Mead region, Nevada: Reply |
| Q36995035 | Kv1.5 is a major component underlying the A-type potassium current in retinal arteriolar smooth muscle. |
| Q31033856 | Machine learning approaches to supporting the identification of photoreceptor-enriched genes based on expression data |
| Q38630620 | MicroRNA-155 promotes resolution of hypoxia-inducible factor 1alpha activity during prolonged hypoxia |
| Q47107821 | MicroRNA-containing extracellular vesicles released from endothelial colony-forming cells modulate angiogenesis during ischaemic retinopathy. |
| Q112706107 | Mini-XT, a miniaturized tagmentation-based protocol for efficient sequencing of SARS-CoV-2 |
| Q21202035 | Molecular analysis of endothelial progenitor cell (EPC) subtypes reveals two distinct cell populations with different identities. |
| Q44922051 | Molecular diagnosis for heterogeneous genetic diseases with targeted high-throughput DNA sequencing applied to retinitis pigmentosa. |
| Q24629855 | Mutation altering the miR-184 seed region causes familial keratoconus with cataract |
| Q51786028 | Mutational Analysis of the Rhodopsin Gene in Sector Retinitis Pigmentosa. |
| Q51189785 | Mutational analysis of MIR184 in sporadic keratoconus and myopia. |
| Q44973305 | Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation. |
| Q37622793 | Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements |
| Q35141770 | Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern Ireland |
| Q34667892 | Prediction and verification of miRNA expression in human and rat retinas. |
| Q33522299 | Prediction of microRNAs affecting mRNA expression during retinal development |
| Q31168175 | RNA-Sequencing data supports the existence of novel VEGFA splicing events but not of VEGFAxxxb isoforms |
| Q50465228 | Rapid quantification of microRNAs in plasma using a fast real-time PCR system. |
| Q54570215 | Retinopathy is reduced during experimental diabetes in a mouse model of outer retinal degeneration. |
| Q54570218 | Rod photoreceptor loss in Rho-/- mice reduces retinal hypoxia and hypoxia-regulated gene expression. |
| Q44295618 | Role of vascular endothelial growth factor and placental growth factors during retinal vascular development and hyaloid regression. |
| Q34360154 | Selective extracellular vesicle-mediated export of an overlapping set of microRNAs from multiple cell types. |
| Q34505062 | Small RNAs from plants, bacteria and fungi within the order Hypocreales are ubiquitous in human plasma |
| Q51361593 | TRPV2 Channels Contribute to Stretch-Activated Cation Currents and Myogenic Constriction in Retinal Arterioles. |
| Q54613860 | VEGF-induced retinal angiogenic signaling is critically dependent on Ca²⁺ signaling by Ca²⁺/calmodulin-dependent protein kinase II. |
| Q42683858 | Whole-mitochondrial genome sequencing in primary open-angle glaucoma using massively parallel sequencing identifies novel and known pathogenic variants. |
Search more.