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David Kavanagh

Showing results (111-120 of 193) with videos related to

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Human Molecular Genetics|March 20, 2015
Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levelsDavid Kavanagh, Yi Yu, Elizabeth C Schramm, et al.
Journal of Medical Internet Research|December 21, 2010
Online alcohol interventions: a systematic reviewAngela White, David Kavanagh, Helen Stallman, et al.
Investigative Ophthalmology & Visual Science|June 10, 2020
Rare Genetic Variants in Complement Factor I Lead to Low FI Plasma Levels Resulting in Increased Risk of Age-Related Macular DegenerationThomas M Hallam, Kevin J Marchbank, Claire L Harris, et al.
Plos One|April 25, 2013
Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32Lucy V Holmes, Lisa Strain, Scott J Staniforth, et al.
Transplantation|July 25, 2024
Kidney Transplantation in Patients With aHUS: A Comparison of Eculizumab Prophylaxis Versus Rescue TherapyCaroline Duineveld, Emily K Glover, Romy N Bouwmeester, et al.
BMC Nephrology|April 19, 2021
Effectiveness of Wellbeing Intervention for Chronic Kidney Disease (WICKD): results of a randomised controlled trialKylie M Dingwall, Michelle Sweet, Alan Cass, et al.
Plos Medicine|March 30, 2011
Mutations in complement regulatory proteins predispose to preeclampsia: a genetic analysis of the PROMISSE cohortJane E Salmon, Cara Heuser, Michael Triebwasser, et al.
Frontiers in Immunology|May 14, 2026
Properdin deficiency or anti-properdin treatment ameliorates disease in the C3 gain-of-function mouse model of atypical haemolytic uraemic syndromeGrace Mallett, Ola Kamala, Isabel Y Pappworth, et al.
Nature Genetics|August 18, 2016
Patterns of genic intolerance of rare copy number variation in 59,898 human exomesDouglas M Ruderfer, Tymor Hamamsy, Monkol Lek, et al.
Molecular Immunology|August 3, 2006
Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndromeAnna Richards, M Kathryn Liszewski, David Kavanagh, et al.
Pageof 20

Showing results (111-120 of 193) with videos related to

Sort By:
Pageof 20
Human Molecular Genetics|March 20, 2015
Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levelsDavid Kavanagh, Yi Yu, Elizabeth C Schramm, et al.
Journal of Medical Internet Research|December 21, 2010
Online alcohol interventions: a systematic reviewAngela White, David Kavanagh, Helen Stallman, et al.
Investigative Ophthalmology & Visual Science|June 10, 2020
Rare Genetic Variants in Complement Factor I Lead to Low FI Plasma Levels Resulting in Increased Risk of Age-Related Macular DegenerationThomas M Hallam, Kevin J Marchbank, Claire L Harris, et al.
Plos One|April 25, 2013
Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32Lucy V Holmes, Lisa Strain, Scott J Staniforth, et al.
Transplantation|July 25, 2024
Kidney Transplantation in Patients With aHUS: A Comparison of Eculizumab Prophylaxis Versus Rescue TherapyCaroline Duineveld, Emily K Glover, Romy N Bouwmeester, et al.
BMC Nephrology|April 19, 2021
Effectiveness of Wellbeing Intervention for Chronic Kidney Disease (WICKD): results of a randomised controlled trialKylie M Dingwall, Michelle Sweet, Alan Cass, et al.
Plos Medicine|March 30, 2011
Mutations in complement regulatory proteins predispose to preeclampsia: a genetic analysis of the PROMISSE cohortJane E Salmon, Cara Heuser, Michael Triebwasser, et al.
Frontiers in Immunology|May 14, 2026
Properdin deficiency or anti-properdin treatment ameliorates disease in the C3 gain-of-function mouse model of atypical haemolytic uraemic syndromeGrace Mallett, Ola Kamala, Isabel Y Pappworth, et al.
Nature Genetics|August 18, 2016
Patterns of genic intolerance of rare copy number variation in 59,898 human exomesDouglas M Ruderfer, Tymor Hamamsy, Monkol Lek, et al.
Molecular Immunology|August 3, 2006
Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndromeAnna Richards, M Kathryn Liszewski, David Kavanagh, et al.
Pageof 20