Neil V Morgan

发表

An adaptable analysis workflow for characterization of platelet spreading and morphology

Iain B Styles, Jeremy A Pike, Steven G Thomas, 2020, Platelets.

Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis–renal dysfunction–cholestasis (ARC) syndrome

Richard C Trembath, Paul Gissen, Colin A. Johnson, 2004, Nature Genetics.

Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism

Michael R. Kendall, M. Karkucak, T. Yakut, 2010, Clinical endocrinology.

Optimised insert design for improved single-molecule imaging and quantification through CRISPR-Cas9 mediated knock-in

Jeremy A Pike, Steven G Thomas, Natalie S Poulter, 2019, Scientific Reports.

CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and Resolution

Jeremy A Pike, Steven G Thomas, Jeremy A. Pike, 2017, Scientific Reports.

Inactivation of IL11 signaling causes craniosynostosis, delayed tooth eruption, and supernumerary teeth.

Sven Kreiborg, Pekka Nieminen, S. Kreiborg, 2011, American journal of human genetics.

Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.

Paul Gissen, Shu-Yuan Cheng, M. Reith, 2009, The Journal of clinical investigation.

HIF activation identifies early lesions in VHL kidneys: evidence for site-specific tumor suppressor function in the nephron.

Charles C Wykoff, Adrian L Harris, A. Harris, 2002, Cancer cell.

Phenotype description and response to thrombopoietin receptor agonist in DIAPH1-related disorder.

Wendy N Erber, Chantal Thys, Kate Downes, 2018, Blood advances.