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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
February 3, 2005
Successful plasma therapy for atypical hemolytic uremic syndrome caused by factor H deficiency owing to a novel mutation in the complement cofactor protein domain 15
Christoph Licht, Annic Weyersberg, Stefan Heinen, et al.
International Journal of Oncology
|
April 20, 2011
Human complement factor H is a novel diagnostic marker for lung adenocarcinoma
Tiantian Cui, Yuan Chen, Thomas Knösel, et al.
Scientific Reports
|
April 7, 2022
Low molecular weight polysialic acid binds to properdin and reduces the activity of the alternative complement pathway
Anahita Shahraz, Yuchen Lin, Joshua Mbroh, et al.
Kidney International Reports
|
June 11, 2020
<i>In situ</i> Visualization of C3/C5 Convertases to Differentiate Complement Activation
Fermin Person, Tim Petschull, Sonia Wulf, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 2, 2003
Successful (?) therapy of hemolytic-uremic syndrome with factor H abnormality
Angela Gerber, Antje H Kirchhoff-Moradpour, Silke Obieglo, et al.
Journal of the American Society of Nephrology : JASN
|
February 7, 2001
The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20
Jessica Caprioli, Paola Bettinaglio, Peter F Zipfel, et al.
Clinical Kidney Journal
|
August 11, 2018
Membranoproliferative glomerulonephritis and C3 glomerulopathy in children: change in treatment modality? A report of a case series
Giuseppina Spartà, Ariana Gaspert, Thomas J Neuhaus, et al.
International Journal of Medical Microbiology : IJMM
|
August 19, 2008
Identification and characterization of the factor H and FHL-1 binding complement regulator-acquiring surface protein 1 of the Lyme disease spirochete Borrelia spielmanii sp. nov
Pia Herzberger, Corinna Siegel, Christine Skerka, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
October 17, 2012
Yersinia enterocolitica YadA mediates complement evasion by recruitment and inactivation of C3 products
Magnus K H Schindler, Monika S Schütz, Melanie C Mühlenkamp, et al.
Kidney International
|
July 18, 2008
C3 deposition glomerulopathy due to a functional factor H defect
Sandra Habbig, Michael J Mihatsch, Stefan Heinen, et al.
Page
of 28
Search research articles
Search
Showing results (161-170 of 273) with videos related to
Sort By:
Page
of 28
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
February 3, 2005
Successful plasma therapy for atypical hemolytic uremic syndrome caused by factor H deficiency owing to a novel mutation in the complement cofactor protein domain 15
Christoph Licht, Annic Weyersberg, Stefan Heinen, et al.
International Journal of Oncology
|
April 20, 2011
Human complement factor H is a novel diagnostic marker for lung adenocarcinoma
Tiantian Cui, Yuan Chen, Thomas Knösel, et al.
Scientific Reports
|
April 7, 2022
Low molecular weight polysialic acid binds to properdin and reduces the activity of the alternative complement pathway
Anahita Shahraz, Yuchen Lin, Joshua Mbroh, et al.
Kidney International Reports
|
June 11, 2020
<i>In situ</i> Visualization of C3/C5 Convertases to Differentiate Complement Activation
Fermin Person, Tim Petschull, Sonia Wulf, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 2, 2003
Successful (?) therapy of hemolytic-uremic syndrome with factor H abnormality
Angela Gerber, Antje H Kirchhoff-Moradpour, Silke Obieglo, et al.
Journal of the American Society of Nephrology : JASN
|
February 7, 2001
The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20
Jessica Caprioli, Paola Bettinaglio, Peter F Zipfel, et al.
Clinical Kidney Journal
|
August 11, 2018
Membranoproliferative glomerulonephritis and C3 glomerulopathy in children: change in treatment modality? A report of a case series
Giuseppina Spartà, Ariana Gaspert, Thomas J Neuhaus, et al.
International Journal of Medical Microbiology : IJMM
|
August 19, 2008
Identification and characterization of the factor H and FHL-1 binding complement regulator-acquiring surface protein 1 of the Lyme disease spirochete Borrelia spielmanii sp. nov
Pia Herzberger, Corinna Siegel, Christine Skerka, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
October 17, 2012
Yersinia enterocolitica YadA mediates complement evasion by recruitment and inactivation of C3 products
Magnus K H Schindler, Monika S Schütz, Melanie C Mühlenkamp, et al.
Kidney International
|
July 18, 2008
C3 deposition glomerulopathy due to a functional factor H defect
Sandra Habbig, Michael J Mihatsch, Stefan Heinen, et al.
Page
of 28