J. Chapple
发表
M. Knight,
C. V. van Blitterswijk,
L. Moroni,
2017,
Acta biomaterialia.
Tyson V. Sharp,
C. Thompson,
M. Knight,
2018,
Endocrine-related cancer.
J. Chapple,
S. O’Toole,
2016,
Biochemical Society transactions.
K. Willison,
P. Adamson,
M. Cheetham,
2003,
The Biochemical journal.
M. Cheetham,
J. Chapple,
2003
.
C. Thompson,
M. Knight,
P. Beales,
2017,
European cells & materials.
M. Cheetham,
A. Hardcastle,
J. Chapple,
2005,
Methods in enzymology.
Arunashree Bhamidipati,
K. Willison,
P. Luthert,
2002,
Human molecular genetics.
K. Willison,
M. Cheetham,
A. Hardcastle,
2000,
Human molecular genetics.
K. Willison,
M. Cheetham,
A. Hardcastle,
2002,
Investigative ophthalmology & visual science.
M. Cheetham,
J. van der Spuy,
J. Chapple,
2005,
Trends in molecular medicine.
P. Luthert,
M. Cheetham,
B. J. Clark,
2002,
Human molecular genetics.
J. Chapple,
P. S. Sen Gupta,
N. Prodromou,
2009,
The Journal of endocrinology.
J. Gallo,
Virginie Bros-Facer,
J. Chapple,
2008,
Neuroscience Letters.
D. A. Parfitt,
D. Campbell,
David A. Parfitt,
2012
.
G. Blatch,
M. Cheetham,
J. Chapple,
2001,
Gene.
C. Thompson,
L. da Cruz,
P. Coffey,
2017,
Human molecular genetics.
A. Clark,
E. Meimaridou,
J. Chapple,
2011,
Molecular endocrinology.
M. Cheetham,
S. Poopalasundaram,
J. van der Spuy,
2004,
Biochemical Society transactions.
M. Gaasenbeek,
R. Banerjee,
D. Hunt,
2005,
Gene.
S. Thorpe,
M. Knight,
J. Connelly,
2015,
Stem cells.
C. Thompson,
M. Knight,
C. Hung,
2015,
Arthritis Research & Therapy.
C. Thompson,
L. da Cruz,
P. Coffey,
2017,
Human molecular genetics.
C. Thompson,
M. Knight,
J. Chapple,
2013,
Cilia.
C. Thompson,
J. Chapple,
M. Knight,
2012,
Journal of Cell Science.
C. Thompson,
M. Knight,
P. Beales,
2012,
Development.
Nuclear translocation of the Hsp70/Hsp90 organizing protein mSTI1 is regulated by cell cycle kinases
G. Blatch,
M. Cheetham,
M. Balda,
2004,
Journal of Cell Science.
B. Brais,
K. Gehring,
B. Gentil,
2018,
FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
C. Thompson,
M. Knight,
P. Beales,
2012,
Journal of cell science.
S. Henson,
A. Akbar,
P. Lavender,
2019,
bioRxiv.
M. Korbonits,
S. Schulz,
A. Grossman,
2012,
The Journal of clinical endocrinology and metabolism.
S. Lovestone,
C. Hooper,
R. Killick,
2007,
Neuroscience Letters.
G. Colombo,
C. Prodromou,
Matteo Castelli,
2022,
bioRxiv.
M. Cheetham,
J. Chapple,
2003,
Journal of Biological Chemistry.
P. Yu-Wai-Man,
M. Cheetham,
J. Chapple,
2022,
Human molecular genetics.
M. Elphick,
T. Webb,
M. Cheetham,
2008,
Endocrinology.
A. Rademaker,
R. Eddy,
T. Shows,
1999,
Cytogenetic and Genome Research.
The binding of the molecular chaperone Hsc70 to the prion protein PrP is modulated by pH and copper.
A. Rhie,
M. Cheetham,
C. Birkett,
2010,
The international journal of biochemistry & cell biology.
R. Pfundt,
M. Reilly,
P. Giunti,
2018,
Brain : a journal of neurology.
M. Reilly,
P. Giunti,
S. Vermeer,
2011
.
J. Uney,
M. Cheetham,
J. Gallo,
2007,
Molecular therapy : the journal of the American Society of Gene Therapy.
E. Leshinsky‐Silver,
D. Lev,
T. Lerman-Sagie,
2015,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
Julian R. E. Davis,
D. Berney,
R. Quinton,
2008,
The Journal of clinical endocrinology and metabolism.
K. Willison,
A. Webster,
M. Cheetham,
2001,
Journal of medical genetics.
Claire Hughes,
L. Metherell,
L. Guasti,
2013,
Molecular and Cellular Endocrinology.
S. Henson,
A. Akbar,
P. Lavender,
2021,
Nature Communications.
T. Webb,
M. Cheetham,
A. Clark,
2009,
Endocrinology.
M. Cheetham,
J. van der Spuy,
J. Chapple,
2015,
Sub-cellular biochemistry.
F. Rüschendorf,
C. Becker,
P. Nürnberg,
2005,
Nature Genetics.
Mutations in Nicotinamide Nucleotide Transhydrogenase (NNT) cause familial glucocorticoid deficiency
F. Wagner,
P. Frommolt,
P. Nürnberg,
2012,
Nature Genetics.
T. Webb,
L. Metherell,
T. Chung,
2008,
The Journal of clinical endocrinology and metabolism.
H. Storr,
K. Koehler,
A. Huebner,
2009,
Molecular endocrinology.
M. Elphick,
T. Webb,
L. Metherell,
2009,
Proceedings of the National Academy of Sciences.
S. Lovestone,
G. Melino,
R. Goodyear,
2006,
Journal of neurochemistry.
G. Blatch,
M. Cheetham,
R. Zimmermann,
2007,
The international journal of biochemistry & cell biology.
M. Cheetham,
J. Höhfeld,
Britta Westhoff,
2005,
Current Biology.
J. Lupski,
S. Fisher,
D. Jagger,
2005,
Nature Genetics.
U. Srirangalingam,
S. Ellard,
M. Korbonits,
2010,
Human mutation.
M. Knight,
J. Chapple,
A. Wann,
2014,
Cellular signalling.
E. Shoubridge,
B. Brais,
M. Duchen,
2012,
Proceedings of the National Academy of Sciences.
T. Webb,
G. Michael,
G. Blatch,
2009,
Human molecular genetics.
M. Korbonits,
A. Grossman,
H. Chahal,
2010,
Trends in Endocrinology & Metabolism.
H. Storr,
K. Koehler,
A. Huebner,
2009
.
I. Coppens,
R. Fleck,
A. Hamacher-Brady,
2018,
bioRxiv.
E. Meimaridou,
J. Chapple,
S. Gooljar,
2008,
Journal of molecular endocrinology.
M. Cheetham,
A. Hardcastle,
J. van der Spuy,
2001,
Trends in molecular medicine.
J. Uney,
M. Cheetham,
J. Gallo,
2007,
Molecular therapy : the journal of the American Society of Gene Therapy.
F. Fitzke,
A. Webster,
M. Cheetham,
2004,
British Journal of Ophthalmology.
C. Thompson,
M. Knight,
J. Chapple,
2014,
Osteoarthritis and cartilage.
C. Thompson,
M. Knight,
P. Beales,
2021,
International journal of molecular sciences.
P. Yu-Wai-Man,
M. Cheetham,
J. van der Spuy,
2021,
Molecular therapy. Nucleic acids.
B. Brais,
P. Giunti,
B. Gentil,
2017,
Human molecular genetics.
G. Michael,
P. Giunti,
S. Vermeer,
2016,
Human molecular genetics.
T. Cooper,
K. Anthony,
J. Gallo,
2007,
Human molecular genetics.
D. Athanasiou,
N. Kanuga,
M. Cheetham,
2012,
Molecular biology of the cell.
T. Webb,
M. Cheetham,
A. Clark,
2008
.
Tammy M. Havener,
Laura E. Herring,
L. Herring,
2021,
bioRxiv.
C. Thompson,
M. Knight,
J. Chapple,
2014,
Osteoarthritis and cartilage.