Richard Stevens

ORCID: 0000-0003-4278-5654
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About
Contact & Profiles
Research Areas
  • Alzheimer's disease research and treatments
  • CRISPR and Genetic Engineering
  • Advanced biosensing and bioanalysis techniques
  • Paraoxonase enzyme and polymorphisms
  • Pesticide Exposure and Toxicity
  • Chromosomal and Genetic Variations
  • Vitamin C and Antioxidants Research
  • Marine Toxins and Detection Methods
  • RNA modifications and cancer
  • Genomics and Phylogenetic Studies
  • Bioactive Natural Diterpenoids Research
  • Tryptophan and brain disorders
  • VLSI and Analog Circuit Testing
  • Diatoms and Algae Research
  • Cytokine Signaling Pathways and Interactions
  • Monoclonal and Polyclonal Antibodies Research
  • Software Testing and Debugging Techniques
  • Analytical Chemistry and Sensors
  • RNA regulation and disease
  • Business Process Modeling and Analysis
  • Advanced Biosensing Techniques and Applications
  • Inflammatory mediators and NSAID effects
  • Salivary Gland Disorders and Functions
  • Nicotinic Acetylcholine Receptors Study
  • Bioinformatics and Genomic Networks

University Foundation
2024

Merck & Co., Inc., Rahway, NJ, USA (United States)
2018-2021

Source BioScience (United Kingdom)
2020

Imperial College Healthcare NHS Trust
2013

GenProMarkers (United States)
2012

Biomark (United States)
2012

University of Washington Medical Center
2006-2010

University of Washington
2005-2010

University Hospitals Sussex NHS Foundation Trust
2008

We developed PolyA-seq, a strand-specific and quantitative method for high-throughput sequencing of 3' ends polyadenylated transcripts, used it to globally map polyadenylation (polyA) sites in 24 matched tissues human, rhesus, dog, mouse, rat. show that PolyA-seq is as accurate existing RNA (RNA-seq) approaches digital gene expression (DGE), enabling simultaneous mapping polyA measurement their usage. In we confirmed 158,533 known discovered 280,857 novel (FDR < 2.5%). On average 10% human...

10.1101/gr.132563.111 article EN cc-by-nc Genome Research 2012-03-27

Saliva provides a useful and noninvasive alternative to blood for many biomedical diagnostic assays. The level of the hormone cortisol in saliva is related stress. We present here development portable surface plasmon resonance (SPR) biosensor system detection saliva. Cortisol-specific monoclonal antibodies were used develop competition assay with six-channel SPR designed our laboratory. limit laboratory buffers was 0.36 ng/mL (1.0 nM). An in-line filter based on diffusion through hollow...

10.1021/ac800892h article EN Analytical Chemistry 2008-07-26

The high-density lipoprotein-associated enzyme paraoxonase 1 (PON1) hydrolyzes lactones, aromatic esters, and neurotoxic organophosphorus (OP) compounds, including insecticide metabolites nerve agents. Experiments with mice lacking PON1 ( −/− mice) have established that plasma protects against chlorpyrifos/chlorpyrifos-oxon diazinon/diazoxon (DZO) exposure but does not protect parathion/paraoxon or catalytic efficiency of determines whether it will a given OP exposure. Expression active...

10.1073/pnas.0805865105 article EN Proceedings of the National Academy of Sciences 2008-08-19

Severe forms of psoriasis can be complicated by systemic microvascular hyperpermeability. Vascular endothelial growth factor (VEGF) possesses potent vascular permeability activity. We suggest that VEGF enters the circulation and acts on microvessels to mediate hyperpermeability.To quantify renal circulating concentration in severe psoriasis, investigate relationship between plasma skin joint involvement.Inception cohort studies patients with generalized pustular plaque psoriasis.St John's...

10.1001/archderm.138.6.791 article EN Archives of Dermatology 2002-06-01

Alzheimer's disease (AD) is a chronic neurodegenerative with pathological hallmarks including the formation of extracellular aggregates amyloid-beta (Aβ) known as plaques and intracellular tau tangles. Coincident Aβ recruitment activation glial cells to plaque forming niche. In addition histological data showing niche, AD genetic studies have added growing appreciation how dysfunctional glia pathways drive neuropathology, emphasis on microglia pathways. Genomic approaches enable comparisons...

10.1186/s12974-018-1265-7 article EN cc-by Journal of Neuroinflammation 2018-09-06

Massively parallel sequencing technologies have made it possible to generate large quantities of sequence data. However, as research-associated information is transferred into clinical practice, cost and throughput constraints generally require sequence-specific targeted analyses. Therefore, sample enrichment methods been developed meet the needs applications. current amplification hybrid capture are limited in contiguous length sequences for which they able enrich. PCR based also loses...

10.1371/journal.pone.0215441 article EN cc-by PLoS ONE 2019-04-18

Aggressive fibromatosis is a rare, benign proliferative disease with unknown aetiology and high recurrence rate. To date, there are only eight reported cases affecting the larynx. Four were managed total laryngectomy, whilst spontaneous regression happened in one case. Spindle cell carcinoma rare but highly aggressive biphasic tumour which often arises head neck. Diagnosed laryngeal more than 10 years ago, our patient had undergone six trans-oral laser debulking procedures. On this occasion,...

10.7759/cureus.74717 article EN Cureus 2024-11-29

Abstract Background SARS-CoV-2 genotyping has been instrumental to monitor virus evolution and transmission during the pandemic. The reliability of information extracted from efforts depends on a number aspects, including quality input material, applied technology potential laboratory-specific biases. These variables must be monitored ensure genotype reliability. current lack guidelines for leads inclusion error-containing genome sequences in studies viral spread evolution. Results We used...

10.1101/2020.12.01.405738 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2020-12-01
Puja Mehta Sue Holder BA Fisher Tonia L. Vincent Kavitha Nadesalingam and 95 more Helen MacIver William Shingler Jyoti Bakshi Sevda Hassan David D’Cruz Anthony K.C. Chan Anna Litwic F McCrae Raghav Seth F McCrae Anupama Nandagudi Elizabeth C. Jury David Isenberg Uma Karjigi Anekwe Somtochukwu Paul Frances Rees Emma O’Dowd W J Kinnear Simon R. Johnson Peter Lanyon Jyoti Bakshi Richard Stevens Nehal Narayan Christopher Marguerie Heather A. Robinson Lorrette Ffolkes F.S. Worsnop L.S. Ostlere Patrick Kiely Chethana Dharmapalaiah N. Hassan Anupama Nandagudi A. Bharadwaj Małgorzata Skibińska Nagui Gendi E. J. Davies Mohamed Akil Rachael Kilding Jagdish Nair Mary Norine Walsh W. Edmund Farrar R. N. Thompson L. Borukhson Charles McFadyen D Singh V. Rajagopal Andrew M. Chan L. Wearn Koh Jason D. Christie L. Croot Mary Gayed Benjamin Disney Suman Singhal K A Grindulis Timothy D. Reynolds K. Conway David M. Williams Jacquelyn A. Quin G. Dean Dennis Churchill Karen Walker‐Bone Iain Goff G Reynolds Matthew Grove P. Patel M. N. Lazarus Federico Roncaroli Carolyn Gabriel Anne Kinderlerer Elena Nikiphorou Frances Hall Ellen Bruce Leanne Gray Maria Krutikov Surabhi Wig Ian N Bruce Maria Antonietta DʼAgostino Richard J. Wakefield Hilde Berner Hammer O. Vittecoq M. Galeazzi P. Balint Emilio Filippucci Ingrid Möller Annamaria Iagnocco Esperanza Naredo Mikkel Østergaard Corine Gaillez W. Kerselaers Kathy Holder Manuela Le Bars Millicent Stone Frances M. K. Williams Lisa E. Wolber Jaro Karppinen

Background: Thoracic aortic aneurysms (TAA) and dissections are not uncommon causes of sudden death in young adults. Loeys-Dietz syndrome (LDS) is a rare, recently described, autosomal dominant, connective tissue disease characterized by aggressive arterial aneurysms, resulting from mutations the transforming growth factor beta (TGFβ) receptor genes TGFBR1 TGFBR2. Mean age at 26.1 years, most often due to dissection. We report an unusually late presentation LDS, diagnosed following elective...

10.1093/rheumatology/ket197 article EN Lara D. Veeken 2013-04-01

The programmable sequence specificity of CRISPR has found uses in gene editing and diagnostics. This manuscript describes an additional application through a family novel DNA enrichment technologies. CAMP (CRISPR Associated Multiplexed PCR) cCAMP (chimeric utilize the Cas9/sgRNA complex to target loci for ligation universal adapter that is used subsequent amplification. cTRACE Targeting Rare Alleles with CRISPR-based Enrichment) also applies this method use addition adapters, however it...

10.1371/journal.pone.0243781 article EN cc-by PLoS ONE 2020-12-23

In recent years, assurance of clonality the production cell line has been emphasized by health authorities during review regulatory submissions. When insufficient is provided, augmented control strategies may be required for a commercial process. this study, we conducted retrospective assessment legacy through analysis subclones from master bank (MCB). Twenty-four were randomly selected based on predetermined acceptance sampling plan. All these share conserved integration junction, thus...

10.1002/btpr.3215 article EN Biotechnology Progress 2021-09-29

Next-generation sequencing (NGS) is quickly replacing other methods for determining expression profiling of RNA as well single-nucleotide variations within the genomes both model organisms and human samples.At Boston facility Merck Research Laboratories, we concentrate on preparation samples where research needs cannot be met by commercial venders.These unmet may due to either availability up-to-date protocols or deadline constraints.In addition validating developing new libraryconstruction...

10.1186/1753-6561-6-s6-p36 article EN cc-by BMC Proceedings 2012-10-01

Individual alignments of UCE loci in nexus format. Loci were aligned using MAFFT and trimmed wtih Gblocks.

10.5061/dryad.5g205/2 article EN 2017-01-01
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