Alice Goode

Contact

• workRoom E73 Medical School
  Queen's Medical Centre
  Nottingham
  NG7 2UH
  UK
• Alice.Goode@nottingham.ac.uk

Biography

After graduating with a first class Biochemistry degree I went on to study for a PhD in Rob Layfield's group investigating the effects of Paget's Disease of Bone-associated p62 mutations on protein structure and function (funded by Arthritis Research UK). Having finished my PhD, I went on to complete a Postdoc in defining the disease mechanism in patients with amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD), conditions in which p62 mutations have also been identified.

I have since switched research groups and now work in the Biomembrane NMR group as the senior research officer focusing on research in characterising the structure, function and assembly of biological membranes.

Recent Publications

• WRIGHT, TAO, REA, SARAH L., GOODE, ALICE, BENNETT, ANDREW J., RATAJCZAK, THOMAS, LONG, JED E., SEARLE, MARK S., GOLDRING, CHRISTOPHER E., PARK, B. KEVIN, COPPLE, IAN M. and LAYFIELD, ROBERT, 2013. The S349T mutation of SQSTM1 links Keap1/Nrf2 signalling to Paget's disease of bone BONE. 52(2), 699-706
• GIANFRANCESCO, FERNANDO, RENDINA, DOMENICO, DI STEFANO, MARCO, MINGIONE, ALESSANDRA, ESPOSITO, TERESA, MERLOTTI, DANIELA, GALLONE, SALVATORE, MAGLIOCCA, SARA, GOODE, ALICE, FORMICOLA, DANIELA, MORELLO, GIOVANNA, LAYFIELD, ROBERT, FRATTINI, ANNALISA, DE FILIPPO, GIANPAOLO, NUTI, RANUCCIO, SEARLE, MARK, STRAZZULLO, PASQUALE, ISAIA, GIANCARLO, MOSSETTI, GIUSEPPE and GENNARI, LUIGI, 2012. A nonsynonymous TNFRSF11A variation increases NF?B activity and the severity of Paget's disease JOURNAL OF BONE AND MINERAL RESEARCH. 27(2), 443-452
• GOODE, A. and LAYFIELD, R., 2010. Recent advances in understanding the molecular basis of Paget disease of bone JOURNAL OF CLINICAL PATHOLOGY. 63(3), 199-203

• View all publications

• WRIGHT, TAO, REA, SARAH L., GOODE, ALICE, BENNETT, ANDREW J., RATAJCZAK, THOMAS, LONG, JED E., SEARLE, MARK S., GOLDRING, CHRISTOPHER E., PARK, B. KEVIN, COPPLE, IAN M. and LAYFIELD, ROBERT, 2013. The S349T mutation of SQSTM1 links Keap1/Nrf2 signalling to Paget's disease of bone BONE. 52(2), 699-706
• GIANFRANCESCO, FERNANDO, RENDINA, DOMENICO, DI STEFANO, MARCO, MINGIONE, ALESSANDRA, ESPOSITO, TERESA, MERLOTTI, DANIELA, GALLONE, SALVATORE, MAGLIOCCA, SARA, GOODE, ALICE, FORMICOLA, DANIELA, MORELLO, GIOVANNA, LAYFIELD, ROBERT, FRATTINI, ANNALISA, DE FILIPPO, GIANPAOLO, NUTI, RANUCCIO, SEARLE, MARK, STRAZZULLO, PASQUALE, ISAIA, GIANCARLO, MOSSETTI, GIUSEPPE and GENNARI, LUIGI, 2012. A nonsynonymous TNFRSF11A variation increases NF?B activity and the severity of Paget's disease JOURNAL OF BONE AND MINERAL RESEARCH. 27(2), 443-452
• GOODE, A. and LAYFIELD, R., 2010. Recent advances in understanding the molecular basis of Paget disease of bone JOURNAL OF CLINICAL PATHOLOGY. 63(3), 199-203