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Jessica Caprioli

Showing results (11-20 of 18) with videos related to

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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 20Jessica Caprioli, Paola Bettinaglio, Peter F Zipfel, et al.
Human Molecular Genetics|October 30, 2003
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the diseaseJessica Caprioli, Federica Castelletti, Sara Bucchioni, et al.
The Journal of Clinical Investigation|April 17, 2003
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndromeTamara Manuelian, Jens Hellwage, Seppo Meri, et al.
Blood|July 20, 2002
von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndromeGiuseppe Remuzzi, Miriam Galbusera, Marina Noris, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2008
Mutations in FN1 cause glomerulopathy with fibronectin depositsFederica Castelletti, Roberta Donadelli, Federica Banterla, et al.
Journal of the American Society of Nephrology : JASN|February 23, 2013
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotypeElena Bresin, Erica Rurali, Jessica Caprioli, et al.
Blood|April 20, 2006
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcomeJessica Caprioli, Marina Noris, Simona Brioschi, et al.
Clinical Journal of the American Society of Nephrology : CJASN|July 3, 2010
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotypeMarina Noris, Jessica Caprioli, Elena Bresin, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
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 20Jessica Caprioli, Paola Bettinaglio, Peter F Zipfel, et al.
Human Molecular Genetics|October 30, 2003
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the diseaseJessica Caprioli, Federica Castelletti, Sara Bucchioni, et al.
The Journal of Clinical Investigation|April 17, 2003
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndromeTamara Manuelian, Jens Hellwage, Seppo Meri, et al.
Blood|July 20, 2002
von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndromeGiuseppe Remuzzi, Miriam Galbusera, Marina Noris, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2008
Mutations in FN1 cause glomerulopathy with fibronectin depositsFederica Castelletti, Roberta Donadelli, Federica Banterla, et al.
Journal of the American Society of Nephrology : JASN|February 23, 2013
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotypeElena Bresin, Erica Rurali, Jessica Caprioli, et al.
Blood|April 20, 2006
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcomeJessica Caprioli, Marina Noris, Simona Brioschi, et al.
Clinical Journal of the American Society of Nephrology : CJASN|July 3, 2010
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotypeMarina Noris, Jessica Caprioli, Elena Bresin, et al.
Pageof 2