Investigating Protein-protein Interactions in Live Cells Using Bioluminescence Resonance Energy Transfer

Por Deriziotis, Pelagia, Graham, Sarah A., Estruch, Sara B., Fisher, Simon E.
Publicado em 2014

The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers

Por Estruch, Sara B., Graham, Sarah A., Deriziotis, Pelagia, Fisher, Simon E.
Publicado no Sci Rep (2016)

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder

Por Estruch, Sara B., Graham, Sarah A., Chinnappa, Swathi M., Deriziotis, Pelagia, Fisher, Simon E.
Publicado no J Neurodev Disord (2016)

Geometry and Adhesion of Extracellular Domains of DC-SIGNR Neck Length Variants Analyzed by Force–Distance Measurements

Por Leckband, Deborah E., Menon, Sindhu, Rosenberg, Kenneth, Graham, Sarah A., Taylor, Maureen E., Drickamer, Kurt
Publicado em 2011

Binding-site geometry and flexibility in DC-SIGN demonstrated with surface force measurements

Por Menon, Sindhu, Rosenberg, Kenneth, Graham, Sarah A., Ward, Eliot M., Taylor, Maureen E., Drickamer, Kurt, Leckband, Deborah E.
Publicado em 2009

Identification of Neutrophil Granule Glycoproteins as Lewis(x)-containing Ligands Cleared by the Scavenger Receptor C-type Lectin

Por Graham, Sarah A., Antonopoulos, Aristotelis, Hitchen, Paul G., Haslam, Stuart M., Dell, Anne, Drickamer, Kurt, Taylor, Maureen E.
Publicado em 2011

Prolectin, a Glycan-binding Receptor on Dividing B Cells in Germinal Centers

Por Graham, Sarah A., Jégouzo, Sabine A. F., Yan, Sheng, Powlesland, Alex S., Brady, Jacob P., Taylor, Maureen E., Drickamer, Kurt
Publicado em 2009

Structural Basis for Langerin Recognition of Diverse Pathogen and Mammalian Glycans through a Single Binding Site

Por Feinberg, Hadar, Taylor, Maureen E., Razi, Nahid, McBride, Ryan, Knirel, Yuriy A., Graham, Sarah A., Drickamer, Kurt, Weis, William I.
Publicado em 2011

Targeted glycoproteomic identification of cancer cell glycosylation

Por Powlesland, Alex S, Hitchen, Paul G, Parry, Simon, Graham, Sarah A, Barrio, Maria Marcela, Elola, Maria Teresa, Mordoh, José, Dell, Anne, Drickamer, Kurt, Taylor, Maureen E
Publicado em 2009

De novo TBR1 mutations in sporadic autism disrupt protein functions

Por Deriziotis, Pelagia, O’Roak, Brian J., Graham, Sarah A., Estruch, Sara B., Dimitropoulou, Danai, Bernier, Raphael A., Gerdts, Jennifer, Shendure, Jay, Eichler, Evan E., Fisher, Simon E.
Publicado em 2014

BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription

Por Dias, Cristina, Estruch, Sara B., Graham, Sarah A., McRae, Jeremy, Sawiak, Stephen J., Hurst, Jane A., Joss, Shelagh K., Holder, Susan E., Morton, Jenny E.V., Turner, Claire, Thevenon, Julien, Mellul, Kelly, Sánchez-Andrade, Gabriela, Ibarra-Soria, Ximena, Deriziotis, Pelagia, Santos, Rui F., Lee, Song-Choon, Faivre, Laurence, Kleefstra, Tjitske, Liu, Pentao, Hurles, Mathew E., Fisher, Simon E., Logan, Darren W.
Publicado no Am J Hum Genet (2016)

Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies

Por Acuna-Hidalgo, Rocio, Deriziotis, Pelagia, Steehouwer, Marloes, Gilissen, Christian, Graham, Sarah A., van Dam, Sipko, Hoover-Fong, Julie, Telegrafi, Aida B., Destree, Anne, Smigiel, Robert, Lambie, Lindsday A., Kayserili, Hülya, Altunoglu, Umut, Lapi, Elisabetta, Uzielli, Maria Luisa, Aracena, Mariana, Nur, Banu G., Mihci, Ercan, Moreira, Lilia M. A., Borges Ferreira, Viviane, Horovitz, Dafne D. G., da Rocha, Katia M., Jezela-Stanek, Aleksandra, Brooks, Alice S., Reutter, Heiko, Cohen, Julie S., Fatemi, Ali, Smitka, Martin, Grebe, Theresa A., Di Donato, Nataliya, Deshpande, Charu, Vandersteen, Anthony, Marques Lourenço, Charles, Dufke, Andreas, Rossier, Eva, Andre, Gwenaelle, Baumer, Alessandra, Spencer, Careni, McGaughran, Julie, Franke, Lude, Veltman, Joris A., De Vries, Bert B. A., Schinzel, Albert, Fisher, Simon E., Hoischen, Alexander, van Bon, Bregje W.
Publicado no PLoS Genet (2017)