Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

John P Atkinson

Showing results (151-160 of 198) with videos related to

Pageof 20
Sort By:
Immunity, Inflammation and Disease|January 5, 2020
Impaired tumor necrosis factor-α secretion by CD4 T cells during respiratory syncytial virus bronchiolitis associated with recurrent wheezeMaleewan Kitcharoensakkul, Leonard B Bacharier, Huiqing Yin-Declue, et al.
Kidney International Reports|July 18, 2019
A Multimodality Approach to Assessing Factor I Genetic Variants in Atypical Hemolytic Uremic SyndromeAnuja Java, Nicola Pozzi, Latisha D Love-Gregory, et al.
Journal of the American Society of Nephrology : JASN|October 17, 2015
A Familial C3GN Secondary to Defective C3 Regulation by Complement Receptor 1 and Complement Factor HSophie Chauvet, Lubka T Roumenina, Sarah Bruneau, et al.
Analytical Biochemistry|February 10, 2015
A quantitative lateral flow assay to detect complement activation in bloodElizabeth C Schramm, Nick R Staten, Zhouning Zhang, et al.
Plos One|April 17, 2012
Lack of evidence from studies of soluble protein fragments that Knops blood group polymorphisms in complement receptor-type 1 are driven by malariaPatience B Tetteh-Quarcoo, Christoph Q Schmidt, Wai-Hong Tham, et al.
Human Molecular Genetics|May 22, 2014
Whole-exome sequencing identifies rare, functional CFH variants in families with macular degenerationYi Yu, Michael P Triebwasser, Edwin K S Wong, et al.
Frontiers in Neurology|December 25, 2025
Longitudinal association of retinal morphology and white matter progression in retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsHenok Getahun, Rajendra S Apte, Wilson X Wang, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|October 9, 2018
Association of Blood Concentrations of Complement Split Product iC3b and Serum C3 With Systemic Lupus Erythematosus Disease ActivityAlfred H J Kim, Vibeke Strand, Deepali P Sen, et al.
Blood|April 12, 2012
Targeting recombinant thrombomodulin fusion protein to red blood cells provides multifaceted thromboprophylaxisSergei Zaitsev, M Anna Kowalska, Michael Neyman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2012
Congenital short bowel syndrome as the presenting symptom in male patients with FLNA mutationsChristine S van der Werf, Yunia Sribudiani, Joke B G M Verheij, et al.
Pageof 20

Showing results (151-160 of 198) with videos related to

Sort By:
Pageof 20
Immunity, Inflammation and Disease|January 5, 2020
Impaired tumor necrosis factor-α secretion by CD4 T cells during respiratory syncytial virus bronchiolitis associated with recurrent wheezeMaleewan Kitcharoensakkul, Leonard B Bacharier, Huiqing Yin-Declue, et al.
Kidney International Reports|July 18, 2019
A Multimodality Approach to Assessing Factor I Genetic Variants in Atypical Hemolytic Uremic SyndromeAnuja Java, Nicola Pozzi, Latisha D Love-Gregory, et al.
Journal of the American Society of Nephrology : JASN|October 17, 2015
A Familial C3GN Secondary to Defective C3 Regulation by Complement Receptor 1 and Complement Factor HSophie Chauvet, Lubka T Roumenina, Sarah Bruneau, et al.
Analytical Biochemistry|February 10, 2015
A quantitative lateral flow assay to detect complement activation in bloodElizabeth C Schramm, Nick R Staten, Zhouning Zhang, et al.
Plos One|April 17, 2012
Lack of evidence from studies of soluble protein fragments that Knops blood group polymorphisms in complement receptor-type 1 are driven by malariaPatience B Tetteh-Quarcoo, Christoph Q Schmidt, Wai-Hong Tham, et al.
Human Molecular Genetics|May 22, 2014
Whole-exome sequencing identifies rare, functional CFH variants in families with macular degenerationYi Yu, Michael P Triebwasser, Edwin K S Wong, et al.
Frontiers in Neurology|December 25, 2025
Longitudinal association of retinal morphology and white matter progression in retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsHenok Getahun, Rajendra S Apte, Wilson X Wang, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|October 9, 2018
Association of Blood Concentrations of Complement Split Product iC3b and Serum C3 With Systemic Lupus Erythematosus Disease ActivityAlfred H J Kim, Vibeke Strand, Deepali P Sen, et al.
Blood|April 12, 2012
Targeting recombinant thrombomodulin fusion protein to red blood cells provides multifaceted thromboprophylaxisSergei Zaitsev, M Anna Kowalska, Michael Neyman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2012
Congenital short bowel syndrome as the presenting symptom in male patients with FLNA mutationsChristine S van der Werf, Yunia Sribudiani, Joke B G M Verheij, et al.
Pageof 20