CRISPR-Mediated Protein Tagging with Nanoluciferase to Investigate Native Chemokine Receptor Function and Conformational Changes

di White, Carl W., Caspar, Birgit, Vanyai, Hannah K., Pfleger, Kevin D.G., Hill, Stephen J.
Pubblicato in Cell Chem Biol (2020)

Using nanoBRET and CRISPR/Cas9 to monitor proximity to a genome-edited protein in real-time

di White, Carl W., Vanyai, Hannah K., See, Heng B., Johnstone, Elizabeth K. M., Pfleger, Kevin D. G.
Pubblicato in Sci Rep (2017)

MOZ Regulates the Tbx1 Locus, and Moz Mutation Partially Phenocopies DiGeorge Syndrome

di Voss, Anne K., Vanyai, Hannah K., Collin, Caitlin, Dixon, Mathew P., McLennan, Tamara J., Sheikh, Bilal N., Scambler, Peter, Thomas, Tim
Pubblicazione 2012

Control of skeletal morphogenesis by the Hippo-YAP/TAZ pathway

di Vanyai, Hannah K., Prin, Fabrice, Guillermin, Oriane, Marzook, Bishara, Boeing, Stefan, Howson, Alexander, Saunders, Rebecca E., Snoeks, Thomas, Howell, Michael, Mohun, Timothy J., Thompson, Barry
Pubblicato in Development (2020)

MOZ and BMI1 play opposing roles during Hox gene activation in ES cells and in body segment identity specification in vivo

di Sheikh, Bilal N., Downer, Natalie L., Phipson, Belinda, Vanyai, Hannah K., Kueh, Andrew J., McCarthy, Davis J., Smyth, Gordon K., Thomas, Tim, Voss, Anne K.
Pubblicato in Proc Natl Acad Sci U S A (2015)

A citizen science model for implementing statewide educational DNA barcoding

di Chiovitti, Anthony, Thorpe, Frazer, Gorman, Christopher, Cuxson, Jennifer L., Robevska, Gorjana, Szwed, Christopher, Duncan, Jacinta C., Vanyai, Hannah K., Cross, Joseph, Siemering, Kirby R., Sumner, Joanna
Pubblicato in PLoS One (2019)

MOZ regulates B-cell progenitors and, consequently, Moz haploinsufficiency dramatically retards MYC-induced lymphoma development

di Sheikh, Bilal N., Lee, Stanley C. W., El-Saafin, Farrah, Vanyai, Hannah K., Hu, Yifang, Pang, Swee Heng Milon, Grabow, Stephanie, Strasser, Andreas, Nutt, Stephen L., Alexander, Warren S., Smyth, Gordon K., Voss, Anne K., Thomas, Tim
Pubblicato in Blood (2015)

De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation

di Haas, Matilda A., Ngo, Linh, Li, Shan Shan, Schleich, Sibylle, Qu, Zhengdong, Vanyai, Hannah K., Cullen, Hayley D., Cardona-Alberich, Aida, Gladwyn-Ng, Ivan E., Pagnamenta, Alistair T., Taylor, Jenny C., Stewart, Helen, Kini, Usha, Duncan, Kent E., Teleman, Aurelio A., Keays, David A., Heng, Julian I.-T.
Pubblicato in Cell Rep (2016)