Dr Seema Qamar

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 - Molecular Basis of Disease

(2010)

1812,

1225

(doi: 10.1016/j.bbadis.2010.11.006)

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,

1582

(doi: 10.1016/j.str.2009.09.013)

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 Sci

(2008)

154

(doi: 10.1002/pro.5560050119)

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,

F950

(doi: 10.1152/ajprenal.90258.2008)

TRP channels and kidney disease: Lessons from polycystic kidney disease

S Qamar, M Vadivelu, R Sandford

– Biochem Soc Trans

(2007)

35,

124

(doi: 10.1042/bst0350124)

The remarkable mechanical strength of polycystin-1 supports a direct role in mechanotransduction.

JR Forman, S Qamar, E Paci, RN Sandford, J Clarke

– J Mol Biol

(2005)

349,

861

(doi: 10.1016/j.jmb.2005.04.008)

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,

585A

(link to publication)

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