Research Associate

Publications

Receptor protein tyrosine phosphatases are novel components of a polycystin complex.
CA Boucher, HH Ward, RL Case, KS Thurston, X Li, A Needham, E Romero, D Hyink, S Qamar, T Roitbak, S Powell, C Ward, PD Wilson, A Wandinger-Ness, RN Sandford
Biochimica et biophysica acta
(2010)
1812
Non-Native Interactions Are Critical for Mechanical Strength in PKD Domains
JR Forman, ZT Yew, S Qamar, RN Sandford, E Paci, J Clarke
Structure (London, England : 1993)
(2009)
17
Identification of arginine 331 as an important active site residue in the Class II fructose‐1,6‐bisphosphate aldolase of Escherichia coli
S Qamar, K Marsh, A Berry
Protein science : a publication of the Protein Society
(2008)
5
Human H+ATPase a4 subunit mutations causing renal tubular acidosis reveal a role for interaction with phosphofructokinase-1
Y Su, KG Blake-Palmer, S Sorrell, B Javid, K Bowers, A Zhou, SH Chang, S Qamar, FE Karet
American journal of physiology. Renal physiology
(2008)
295
TRP channels and kidney disease: lessons from polycystic kidney disease.
S Qamar, M Vadivelu, R Sandford
Biochemical Society Transactions
(2007)
35
The remarkable mechanical strength of polycystin-1 supports a direct role in mechanotransduction.
JR Forman, S Qamar, E Paci, RN Sandford, J Clarke
Journal of Molecular Biology
(2005)
349
The remarkable mechanical strength of polycystin-1 suggests a novel mechanism for mechanotransduction
JR Forman, S Qamar, RN Sandford, J Clarke
BIOPHYSICAL JOURNAL
(2005)
88

Research Group

Telephone number

01223 336359

Email address