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

Elena Volokhina

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
Frontiers in Immunology|March 15, 2021
Editorial: Complement and ImmunotherapeuticsMarcin Okrój, Elena Volokhina
BMJ Case Reports|February 17, 2016
Recovery of renal function after long-term dialysis and resolution of cardiomyopathy in a patient with aHUS receiving eculizumabKhadizha Emirova, Elena Volokhina, Evgenia Tolstova, et al.
Autoimmunity|January 9, 2018
Gain of function mutant of complement factor B K323E mimics pathogenic C3NeF autoantibodies in convertase assaysAleksandra Urban, Anna Borowska, Anna Felberg, et al.
Pediatric Nephrology (Berlin, Germany)|June 7, 2012
Novel C3 mutation p.Lys65Gln in aHUS affects complement factor H bindingElena Volokhina, Dineke Westra, Xiaoguang Xue, et al.
The Journal of Allergy and Clinical Immunology|March 2, 2020
Gain-of-function mutation in complement C2 protein identified in a patient with aHUSAleksandra Urban, Elena Volokhina, Anna Felberg, et al.
Pediatric Nephrology (Berlin, Germany)|June 1, 2016
Fecal diagnostics in combination with serology: best test to establish STEC-HUSKioa L Wijnsma, Sheila A M van Bommel, Thea van der Velden, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 29, 2010
Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS)Dineke Westra, Elena Volokhina, Eefje van der Heijden, et al.
Journal of Human Genetics|December 8, 2017
Genetic predisposition to infection in a case of atypical hemolytic uremic syndromeLambertus van den Heuvel, Kristian Riesbeck, Omaima El Tahir, et al.
The EMBO Journal|March 26, 2016
Regulators of complement activity mediate inhibitory mechanisms through a common C3b-binding modeFederico Forneris, Jin Wu, Xiaoguang Xue, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 4, 2018
Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 GlomerulopathyAmy J Osborne, Matteo Breno, Nicolo Ghiringhelli Borsa, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Frontiers in Immunology|March 15, 2021
Editorial: Complement and ImmunotherapeuticsMarcin Okrój, Elena Volokhina
BMJ Case Reports|February 17, 2016
Recovery of renal function after long-term dialysis and resolution of cardiomyopathy in a patient with aHUS receiving eculizumabKhadizha Emirova, Elena Volokhina, Evgenia Tolstova, et al.
Autoimmunity|January 9, 2018
Gain of function mutant of complement factor B K323E mimics pathogenic C3NeF autoantibodies in convertase assaysAleksandra Urban, Anna Borowska, Anna Felberg, et al.
Pediatric Nephrology (Berlin, Germany)|June 7, 2012
Novel C3 mutation p.Lys65Gln in aHUS affects complement factor H bindingElena Volokhina, Dineke Westra, Xiaoguang Xue, et al.
The Journal of Allergy and Clinical Immunology|March 2, 2020
Gain-of-function mutation in complement C2 protein identified in a patient with aHUSAleksandra Urban, Elena Volokhina, Anna Felberg, et al.
Pediatric Nephrology (Berlin, Germany)|June 1, 2016
Fecal diagnostics in combination with serology: best test to establish STEC-HUSKioa L Wijnsma, Sheila A M van Bommel, Thea van der Velden, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 29, 2010
Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS)Dineke Westra, Elena Volokhina, Eefje van der Heijden, et al.
Journal of Human Genetics|December 8, 2017
Genetic predisposition to infection in a case of atypical hemolytic uremic syndromeLambertus van den Heuvel, Kristian Riesbeck, Omaima El Tahir, et al.
The EMBO Journal|March 26, 2016
Regulators of complement activity mediate inhibitory mechanisms through a common C3b-binding modeFederico Forneris, Jin Wu, Xiaoguang Xue, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 4, 2018
Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 GlomerulopathyAmy J Osborne, Matteo Breno, Nicolo Ghiringhelli Borsa, et al.
Pageof 2