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G Shuttleworth

Showing results (21-30 of 26) with videos related to

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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.
International Journal of Molecular Sciences|August 27, 2021
MiR-126-3p Is Dynamically Regulated in Endothelial-to-Mesenchymal Transition during FibrosisNina P Jordan, Samuel J Tingle, Victoria G Shuttleworth, et al.
Frontiers in Immunology|January 16, 2023
A novel method for real-time analysis of the complement C3b:FH:FI complex reveals dominant negative <i>CFI</i> variants in age-related macular degenerationThomas M Hallam, Thomas E Cox, Kate Smith-Jackson, et al.
American Journal of Human Genetics|October 24, 2001
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndromeS Kenwrick, H Woffendin, T Jakins, et al.
Human Molecular Genetics|March 30, 2021
The rare C9 P167S risk variant for age-related macular degeneration increases polymerization of the terminal component of the complement cascadeO McMahon, T M Hallam, S Patel, et al.
Science Immunology|December 15, 2019
Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in <i>STAT2</i>Christopher J A Duncan, Benjamin J Thompson, Rui Chen, et al.
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Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
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.
International Journal of Molecular Sciences|August 27, 2021
MiR-126-3p Is Dynamically Regulated in Endothelial-to-Mesenchymal Transition during FibrosisNina P Jordan, Samuel J Tingle, Victoria G Shuttleworth, et al.
Frontiers in Immunology|January 16, 2023
A novel method for real-time analysis of the complement C3b:FH:FI complex reveals dominant negative <i>CFI</i> variants in age-related macular degenerationThomas M Hallam, Thomas E Cox, Kate Smith-Jackson, et al.
American Journal of Human Genetics|October 24, 2001
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndromeS Kenwrick, H Woffendin, T Jakins, et al.
Human Molecular Genetics|March 30, 2021
The rare C9 P167S risk variant for age-related macular degeneration increases polymerization of the terminal component of the complement cascadeO McMahon, T M Hallam, S Patel, et al.
Science Immunology|December 15, 2019
Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in <i>STAT2</i>Christopher J A Duncan, Benjamin J Thompson, Rui Chen, et al.
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