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

nork White, Carl W., Caspar, Birgit, Vanyai, Hannah K., Pfleger, Kevin D.G., Hill, Stephen J.
Argitaratua izan da Cell Chem Biol (2020)

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

nork White, Carl W., Vanyai, Hannah K., See, Heng B., Johnstone, Elizabeth K. M., Pfleger, Kevin D. G.
Argitaratua izan da Sci Rep (2017)

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

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

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

nork 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
Argitaratua izan da Development (2020)

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

nork 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.
Argitaratua izan da Proc Natl Acad Sci U S A (2015)

A citizen science model for implementing statewide educational DNA barcoding

nork 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
Argitaratua izan da PLoS One (2019)

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

nork 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
Argitaratua izan da Blood (2015)

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

nork 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.
Argitaratua izan da Cell Rep (2016)