J. Cavey

发表

Independent interactions of ubiquitin-binding domains in a ubiquitin-mediated ternary complex.

J. Strachan, M. Searle, R. Layfield, 2011, Biochemistry.

Structure of the Ubiquitin-associated Domain of p62 (SQSTM1) and Implications for Mutations That Cause Paget's Disease of Bone*

M. Searle, R. Layfield, Barbara Ciani, 2003, Journal of Biological Chemistry.

Immunoreactivity to Lys63-linked polyubiquitin is a feature of neurodegeneration

J. Lowe, L. Bedford, R. Mayer, 2009, Neuroscience Letters.

Mutant p62/SQSTM1 UBA domains linked to Paget's disease of bone differ in their abilities to function as stabilization signals

S. Ralston, M. Searle, R. Layfield, 2010, FEBS letters.

Loss of Ubiquitin Binding Is a Unifying Mechanism by Which Mutations of SQSTM1 Cause Paget’s Disease of Bone

S. Ralston, M. Searle, R. Layfield, 2006, Calcified Tissue International.

Novel UBA Domain Mutations of SQSTM1 in Paget's Disease of Bone: Genotype Phenotype Correlation, Functional Analysis, and Structural Consequences

L. Hocking, S. Ralston, G. Lucas, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Characterization of a Non‐UBA Domain Missense Mutation of Sequestosome 1 (SQSTM1) in Paget's Disease of Bone

M. Brandi, M. Searle, R. Layfield, 2009, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

p62 mutations, ubiquitin recognition and Paget's disease of bone.

S. Ralston, M. Searle, R. Layfield, 2006, Biochemical Society transactions.

Structural and functional studies of mutations affecting the UBA domain of SQSTM1 (p62) which cause Paget's disease of bone.

L. Hocking, S. Ralston, M. Searle, 2004, Biochemical Society transactions.

Identification of Escherichia coli ygaQ and rpmG as novel mitomycin C resistance factors implicated in DNA repair

E. Bolt, J. Cavey, Tabitha Jenkins, 2015, Bioscience reports.

Ubiquitin Recognition by the Ubiquitin-associated Domain of p62 Involves a Novel Conformational Switch*

S. Ralston, M. Searle, R. Layfield, 2008, Journal of Biological Chemistry.

On the role of STAT1 and STAT6 ADP-ribosylation in the regulation of macrophage activation

U. Vinkemeier, A. Begitt, J. Cavey, 2018, Nature Communications.

Defective recognition of LC3B by mutant SQSTM1/p62 implicates impairment of autophagy as a pathogenic mechanism in ALS-FTLD

Robert Layfield, Terje Johansen, Barry Shaw, 2016, Autophagy.

p 62 mutations , ubiquitin recognition and Paget ’ s disease of bone

S. Ralston, M. Searle, R. Layfield, 2006 .

Role of ubiquitin-mediated proteolysis in the pathogenesis of neurodegenerative disorders

James Lowe, Robert Layfield, J. Lowe, 2003, Ageing Research Reviews.

Loss of Ubiquitin‐Binding Associated With Paget's Disease of Bone p62 (SQSTM1) Mutations

L. Hocking, S. Ralston, M. Searle, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

A family-wide assessment of latent STAT transcription factor interactions reveals divergent dimer repertoires

U. Vinkemeier, Sebastian Krause, A. Begitt, 2023, The Journal of biological chemistry.

Structural insights into specificity and diversity in mechanisms of ubiquitin recognition by ubiquitin-binding domains.

J. Strachan, M. Searle, R. Layfield, 2012, Biochemical Society transactions.

Independent interactions of ubiquitin-binding domains in a ubiquitin-mediated ternary complex.

J. Strachan, M. Searle, R. Layfield, 2011, Biochemistry.

Characterization of a Non‐UBA Domain Missense Mutation of Sequestosome 1 (SQSTM1) in Paget's Disease of Bone

M. Brandi, M. Searle, R. Layfield, 2009, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.