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Showing results (91-100 of 137) with videos related to

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Clinical Journal of the American Society of Nephrology : CJASN|March 29, 2011
Primary, nonsyndromic vesicoureteric reflux and nephropathy in sibling pairs: a United Kingdom cohort for a DNA bankHeather J Lambert, Aisling Stewart, Ambrose M Gullett, et al.
Journal of Medical Case Reports|May 1, 2015
Plasma resistant atypical hemolytic uremic syndrome associated with a CFH mutation treated with eculizumab: a case reportMustafa Sevinc, Taner Basturk, Tuncay Sahutoglu, et al.
American Journal of Human Genetics|July 1, 1996
Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndromeH F Sutherland, R Wadey, J M McKie, et al.
Genomics|July 1, 1996
The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16M H Polymeropoulos, S E Ide, M Wright, et al.
Blood|November 8, 2011
A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndromeNigel J Francis, Bairbre McNicholas, Atif Awan, et al.
Molecular Immunology|June 29, 2007
Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndromeDavid Kavanagh, Anna Richards, Marina Noris, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|December 3, 2009
Successful renal transplantation in factor H autoantibody associated HUS with CFHR1 and 3 deficiency and CFH variant G2850TA M Waters, I Pappworth, K Marchbank, et al.
Clinical Genetics|November 15, 2006
Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardationM Field, P Tarpey, J Boyle, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 10, 2010
Non-atheromatous arterial stenoses in atypical haemolytic uraemic syndrome associated with complement dysregulationChantal Loirat, Marie-Alice Macher, Monique Elmaleh-Berges, et al.
Molecular Immunology|March 23, 2010
Impact of compound heterozygous complement factor H mutations on development of atypical hemolytic uremic syndrome-A pedigree revisitedS A Johnson, J M Williams, S Hakobyan, et al.
Pageof 14

Showing results (91-100 of 137) with videos related to

Sort By:
Pageof 14
Clinical Journal of the American Society of Nephrology : CJASN|March 29, 2011
Primary, nonsyndromic vesicoureteric reflux and nephropathy in sibling pairs: a United Kingdom cohort for a DNA bankHeather J Lambert, Aisling Stewart, Ambrose M Gullett, et al.
Journal of Medical Case Reports|May 1, 2015
Plasma resistant atypical hemolytic uremic syndrome associated with a CFH mutation treated with eculizumab: a case reportMustafa Sevinc, Taner Basturk, Tuncay Sahutoglu, et al.
American Journal of Human Genetics|July 1, 1996
Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndromeH F Sutherland, R Wadey, J M McKie, et al.
Genomics|July 1, 1996
The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16M H Polymeropoulos, S E Ide, M Wright, et al.
Blood|November 8, 2011
A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndromeNigel J Francis, Bairbre McNicholas, Atif Awan, et al.
Molecular Immunology|June 29, 2007
Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndromeDavid Kavanagh, Anna Richards, Marina Noris, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|December 3, 2009
Successful renal transplantation in factor H autoantibody associated HUS with CFHR1 and 3 deficiency and CFH variant G2850TA M Waters, I Pappworth, K Marchbank, et al.
Clinical Genetics|November 15, 2006
Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardationM Field, P Tarpey, J Boyle, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 10, 2010
Non-atheromatous arterial stenoses in atypical haemolytic uraemic syndrome associated with complement dysregulationChantal Loirat, Marie-Alice Macher, Monique Elmaleh-Berges, et al.
Molecular Immunology|March 23, 2010
Impact of compound heterozygous complement factor H mutations on development of atypical hemolytic uremic syndrome-A pedigree revisitedS A Johnson, J M Williams, S Hakobyan, et al.
Pageof 14