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

по White, Carl W., Caspar, Birgit, Vanyai, Hannah K., Pfleger, Kevin D.G., Hill, Stephen J.
Опубликовано в: Cell Chem Biol (2020)

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

по White, Carl W., Vanyai, Hannah K., See, Heng B., Johnstone, Elizabeth K. M., Pfleger, Kevin D. G.
Опубликовано в: Sci Rep (2017)

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

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

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

по 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
Опубликовано в: Development (2020)

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

по 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.
Опубликовано в: Proc Natl Acad Sci U S A (2015)

A citizen science model for implementing statewide educational DNA barcoding

по 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
Опубликовано в: PLoS One (2019)

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

по 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
Опубликовано в: Blood (2015)

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

по 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.
Опубликовано в: Cell Rep (2016)