J. Chapple

发表

HSJ1 Is a Neuronal Shuttling Factor for the Sorting of Chaperone Clients to the Proteasome

M. Cheetham, J. Höhfeld, Britta Westhoff, 2005, Current Biology.

Clinical, genetic and molecular characterization of patients with familial isolated pituitary adenomas (FIPA)

M. Korbonits, A. Grossman, H. Chahal, 2010, Trends in Endocrinology & Metabolism.

From hatching to dispatching: the multiple cellular roles of the Hsp70 molecular chaperone machinery.

E. Meimaridou, J. Chapple, S. Gooljar, 2008, Journal of molecular endocrinology.

Identification and characterization of a human mitochondrial homologue of the bacterial co-chaperone GrpE.

G. Blatch, M. Cheetham, J. Chapple, 2001, Gene.

Can faulty antennae increase adiposity? The link between cilia proteins and obesity.

J. Chapple, P. S. Sen Gupta, N. Prodromou, 2009, The Journal of endocrinology.

Mutations in Nicotinamide Nucleotide Transhydrogenase (NNT) cause familial glucocorticoid deficiency

F. Wagner, P. Frommolt, P. Nürnberg, 2012, Nature Genetics.

Familial glucocorticoid deficiency: New genes and mechanisms

Claire Hughes, L. Metherell, L. Guasti, 2013, Molecular and Cellular Endocrinology.

Can faulty antennae increase adiposity? The link between cilia proteins and obesity.

P. S. Sen Gupta, Natalia V. Prodromou, J. Chapple, 2009, The Journal of endocrinology.

Familial glucocorticoid deficiency: New genes and mechanisms

Claire Hughes, L. Metherell, L. Guasti, 2013, Molecular and Cellular Endocrinology.

The role of HSP70 and its co-chaperones in protein misfolding, aggregation and disease.

M. Cheetham, J. van der Spuy, J. Chapple, 2015, Sub-cellular biochemistry.

Characterization of Aryl Hydrocarbon Receptor Interacting Protein (AIP) Mutations in Familial Isolated Pituitary Adenoma Families

U. Srirangalingam, S. Ellard, M. Korbonits, 2010, Human mutation.