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Plos Medicine
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November 2, 2006
Atypical haemolytic uraemic syndrome associated with a hybrid complement gene
Julian P Venables, Lisa Strain, Danny Routledge, et al.
Journal of the American Society of Nephrology : JASN
|
October 23, 2015
A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic Syndrome
Rachel C Challis, Geisilaine S R Araujo, Edwin K S Wong, et al.
Human Mutation
|
November 8, 2006
The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models
Rebecca E Saunders, Cynthia Abarrategui-Garrido, Véronique Frémeaux-Bacchi, et al.
Investigative Ophthalmology & Visual Science
|
July 2, 2010
Complement factor h autoantibodies and age-related macular degeneration
Baljean Dhillon, Alan F Wright, Adnan Tufail, et al.
Journal of the American Society of Nephrology : JASN
|
December 16, 2016
Thrombotic Microangiopathy in Inverted Formin 2<i>-</i>Mediated Renal Disease
Rachel C Challis, Troels Ring, Yaobo Xu, et al.
Molecular Immunology
|
June 23, 2012
Factor H autoantibodies in membranoproliferative glomerulonephritis
Timothy H J Goodship, Isabel Y Pappworth, Tibor Toth, et al.
Scientific Reports
|
January 10, 2018
Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux
John M Darlow, Rebecca Darlay, Mark G Dobson, et al.
Journal of the American Society of Nephrology : JASN
|
April 12, 2014
Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN
Edwin K S Wong, Holly E Anderson, Andrew P Herbert, et al.
Scientific Reports
|
November 4, 2017
Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux
John M Darlow, Rebecca Darlay, Mark G Dobson, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 24, 2011
Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7
K van Engelen, A V Postma, J B A van de Meerakker, et al.
Page
of 14
Search research articles
Search
Showing results (121-130 of 137) with videos related to
Sort By:
Page
of 14
Plos Medicine
|
November 2, 2006
Atypical haemolytic uraemic syndrome associated with a hybrid complement gene
Julian P Venables, Lisa Strain, Danny Routledge, et al.
Journal of the American Society of Nephrology : JASN
|
October 23, 2015
A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic Syndrome
Rachel C Challis, Geisilaine S R Araujo, Edwin K S Wong, et al.
Human Mutation
|
November 8, 2006
The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models
Rebecca E Saunders, Cynthia Abarrategui-Garrido, Véronique Frémeaux-Bacchi, et al.
Investigative Ophthalmology & Visual Science
|
July 2, 2010
Complement factor h autoantibodies and age-related macular degeneration
Baljean Dhillon, Alan F Wright, Adnan Tufail, et al.
Journal of the American Society of Nephrology : JASN
|
December 16, 2016
Thrombotic Microangiopathy in Inverted Formin 2<i>-</i>Mediated Renal Disease
Rachel C Challis, Troels Ring, Yaobo Xu, et al.
Molecular Immunology
|
June 23, 2012
Factor H autoantibodies in membranoproliferative glomerulonephritis
Timothy H J Goodship, Isabel Y Pappworth, Tibor Toth, et al.
Scientific Reports
|
January 10, 2018
Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux
John M Darlow, Rebecca Darlay, Mark G Dobson, et al.
Journal of the American Society of Nephrology : JASN
|
April 12, 2014
Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN
Edwin K S Wong, Holly E Anderson, Andrew P Herbert, et al.
Scientific Reports
|
November 4, 2017
Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux
John M Darlow, Rebecca Darlay, Mark G Dobson, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 24, 2011
Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7
K van Engelen, A V Postma, J B A van de Meerakker, et al.
Page
of 14