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Isabel Y Pappworth

Showing results (11-20 of 18) with videos related to

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The Journal of Clinical Investigation|February 5, 2019
Hyperfunctional complement C3 promotes C5-dependent atypical hemolytic uremic syndrome in miceKate Smith-Jackson, Yi Yang, Harriet Denton, et al.
Frontiers in Immunology|May 31, 2021
Murine Factor H Co-Produced in Yeast With Protein Disulfide Isomerase Ameliorated C3 Dysregulation in Factor H-Deficient MiceHeather Kerr, Andrew P Herbert, Elisavet Makou, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 7, 2012
Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?David Kavanagh, Isabel Y Pappworth, Holly Anderson, et al.
Molecular Immunology|August 25, 2014
Autoantibodies to CD59, CD55, CD46 or CD35 are not associated with atypical haemolytic uraemic syndrome (aHUS)Rachael Watson, Emma Wearmouth, Amy-Claire McLoughlin, et al.
Immunobiology|January 22, 2016
Selectivity of C3-opsonin targeted complement inhibitors: A distinct advantage in the protection of erythrocytes from paroxysmal nocturnal hemoglobinuria patientsChristoph Q Schmidt, Markus J Harder, Eva-Maria Nichols, et al.
Frontiers in Immunology|December 27, 2021
Homodimeric Minimal Factor H: <i>In Vivo</i> Tracking and Extended Dosing Studies in Factor H Deficient MiceOla Kamala, Talat H Malik, Thomas M Hallam, et al.
Molecular Immunology|June 23, 2012
Factor H autoantibodies in membranoproliferative glomerulonephritisTimothy H J Goodship, Isabel Y Pappworth, Tibor Toth, et al.
Clinical Journal of the American Society of Nephrology : CJASN|September 23, 2021
C3 Glomerulopathy and Related Disorders in Children: Etiology-Phenotype Correlation and OutcomesEdwin K S Wong, Kevin J Marchbank, Hannah Lomax-Browne, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
The Journal of Clinical Investigation|February 5, 2019
Hyperfunctional complement C3 promotes C5-dependent atypical hemolytic uremic syndrome in miceKate Smith-Jackson, Yi Yang, Harriet Denton, et al.
Frontiers in Immunology|May 31, 2021
Murine Factor H Co-Produced in Yeast With Protein Disulfide Isomerase Ameliorated C3 Dysregulation in Factor H-Deficient MiceHeather Kerr, Andrew P Herbert, Elisavet Makou, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 7, 2012
Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?David Kavanagh, Isabel Y Pappworth, Holly Anderson, et al.
Molecular Immunology|August 25, 2014
Autoantibodies to CD59, CD55, CD46 or CD35 are not associated with atypical haemolytic uraemic syndrome (aHUS)Rachael Watson, Emma Wearmouth, Amy-Claire McLoughlin, et al.
Immunobiology|January 22, 2016
Selectivity of C3-opsonin targeted complement inhibitors: A distinct advantage in the protection of erythrocytes from paroxysmal nocturnal hemoglobinuria patientsChristoph Q Schmidt, Markus J Harder, Eva-Maria Nichols, et al.
Frontiers in Immunology|December 27, 2021
Homodimeric Minimal Factor H: <i>In Vivo</i> Tracking and Extended Dosing Studies in Factor H Deficient MiceOla Kamala, Talat H Malik, Thomas M Hallam, et al.
Molecular Immunology|June 23, 2012
Factor H autoantibodies in membranoproliferative glomerulonephritisTimothy H J Goodship, Isabel Y Pappworth, Tibor Toth, et al.
Clinical Journal of the American Society of Nephrology : CJASN|September 23, 2021
C3 Glomerulopathy and Related Disorders in Children: Etiology-Phenotype Correlation and OutcomesEdwin K S Wong, Kevin J Marchbank, Hannah Lomax-Browne, et al.
Pageof 2