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Advances in Chronic Kidney Disease
|
June 20, 2020
Genetic and Protein Structural Evaluation of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy
Stephen J Perkins
Biochemical Society Transactions
|
January 23, 2008
Structure determinations of human and chimaeric antibodies by solution scattering and constrained molecular modelling
Stephen J Perkins, Alexandra Bonner
Journal of Applied Crystallography
|
June 20, 2015
<i>SCT</i>: a suite of programs for comparing atomistic models with small-angle scattering data
David W Wright, Stephen J Perkins
Human Mutation
|
December 7, 2007
CoagMDB: a database analysis of missense mutations within four conserved domains in five vitamin K-dependent coagulation serine proteases using a text-mining tool
Rebecca E Saunders, Stephen J Perkins
Seminars in Thrombosis and Hemostasis
|
April 1, 2006
A user's guide to the interactive Web database of factor H-associated hemolytic uremic syndrome
Rebecca E Saunders, Stephen J Perkins
The Biochemical Journal
|
July 30, 2010
Self-association and domain rearrangements between complement C3 and C3u provide insight into the activation mechanism of C3
Keying Li, Jayesh Gor, Stephen J Perkins
Journal of Molecular Biology
|
February 20, 2002
Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding site
Stephen J Perkins, Timothy H J Goodship
Journal of Molecular Biology
|
December 7, 2007
Implications of the progressive self-association of wild-type human factor H for complement regulation and disease
Ruodan Nan, Jayesh Gor, Stephen J Perkins
TH Open : Companion Journal to Thrombosis and Haemostasis
|
January 21, 2022
Analysis of 272 Genetic Variants in the Upgraded Interactive FXI Web Database Reveals New Insights into FXI Deficiency
Victoria A Harris, Weining Lin, Stephen J Perkins
TH Open : Companion Journal to Thrombosis and Haemostasis
|
January 21, 2022
Analysis of 180 Genetic Variants in a New Interactive FX Variant Database Reveals Novel Insights into FX Deficiency
Victoria A Harris, Weining Lin, Stephen J Perkins
Page
of 11
Search research articles
Search
Showing results (1-10 of 109) with videos related to
Sort By:
Page
of 11
Advances in Chronic Kidney Disease
|
June 20, 2020
Genetic and Protein Structural Evaluation of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy
Stephen J Perkins
Biochemical Society Transactions
|
January 23, 2008
Structure determinations of human and chimaeric antibodies by solution scattering and constrained molecular modelling
Stephen J Perkins, Alexandra Bonner
Journal of Applied Crystallography
|
June 20, 2015
<i>SCT</i>: a suite of programs for comparing atomistic models with small-angle scattering data
David W Wright, Stephen J Perkins
Human Mutation
|
December 7, 2007
CoagMDB: a database analysis of missense mutations within four conserved domains in five vitamin K-dependent coagulation serine proteases using a text-mining tool
Rebecca E Saunders, Stephen J Perkins
Seminars in Thrombosis and Hemostasis
|
April 1, 2006
A user's guide to the interactive Web database of factor H-associated hemolytic uremic syndrome
Rebecca E Saunders, Stephen J Perkins
The Biochemical Journal
|
July 30, 2010
Self-association and domain rearrangements between complement C3 and C3u provide insight into the activation mechanism of C3
Keying Li, Jayesh Gor, Stephen J Perkins
Journal of Molecular Biology
|
February 20, 2002
Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding site
Stephen J Perkins, Timothy H J Goodship
Journal of Molecular Biology
|
December 7, 2007
Implications of the progressive self-association of wild-type human factor H for complement regulation and disease
Ruodan Nan, Jayesh Gor, Stephen J Perkins
TH Open : Companion Journal to Thrombosis and Haemostasis
|
January 21, 2022
Analysis of 272 Genetic Variants in the Upgraded Interactive FXI Web Database Reveals New Insights into FXI Deficiency
Victoria A Harris, Weining Lin, Stephen J Perkins
TH Open : Companion Journal to Thrombosis and Haemostasis
|
January 21, 2022
Analysis of 180 Genetic Variants in a New Interactive FX Variant Database Reveals Novel Insights into FX Deficiency
Victoria A Harris, Weining Lin, Stephen J Perkins
Page
of 11