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J A Goodship

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Kidney International|April 29, 1998
Genetic studies into inherited and sporadic hemolytic uremic syndromeP Warwicker, T H Goodship, R L Donne, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 27, 1999
Familial relapsing haemolytic uraemic syndrome and complement factor H deficiencyP Warwicker, R L Donne, J A Goodship, et al.
Journal of Medical Genetics|March 24, 2005
The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohortsV Fremeaux-Bacchi, E J Kemp, J A Goodship, et al.
Lancet (London, England)|May 9, 1992
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locusP J Scambler, D Kelly, E Lindsay, et al.
American Journal of Human Genetics|February 15, 2001
Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognitionA Richards, M R Buddles, R L Donne, et al.
Molecular Immunology|March 21, 2007
The decay accelerating factor mutation I197V found in hemolytic uraemic syndrome does not impair complement regulationD Kavanagh, R Burgess, D Spitzer, et al.
American Journal of Human Genetics|November 1, 1992
A prospective cytogenetic study of 36 cases of DiGeorge syndromeD I Wilson, I E Cross, J A Goodship, et al.
Journal of Dental Research|January 15, 2013
Evc regulates a symmetrical response to Shh signaling in molar developmentM Nakatomi, M Hovorakova, A Gritli-Linde, et al.
British Heart Journal|October 1, 1991
DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal originD I Wilson, I E Cross, J A Goodship, et al.
American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Kidney International|April 29, 1998
Genetic studies into inherited and sporadic hemolytic uremic syndromeP Warwicker, T H Goodship, R L Donne, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 27, 1999
Familial relapsing haemolytic uraemic syndrome and complement factor H deficiencyP Warwicker, R L Donne, J A Goodship, et al.
Journal of Medical Genetics|March 24, 2005
The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohortsV Fremeaux-Bacchi, E J Kemp, J A Goodship, et al.
Lancet (London, England)|May 9, 1992
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locusP J Scambler, D Kelly, E Lindsay, et al.
American Journal of Human Genetics|February 15, 2001
Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognitionA Richards, M R Buddles, R L Donne, et al.
Molecular Immunology|March 21, 2007
The decay accelerating factor mutation I197V found in hemolytic uraemic syndrome does not impair complement regulationD Kavanagh, R Burgess, D Spitzer, et al.
American Journal of Human Genetics|November 1, 1992
A prospective cytogenetic study of 36 cases of DiGeorge syndromeD I Wilson, I E Cross, J A Goodship, et al.
Journal of Dental Research|January 15, 2013
Evc regulates a symmetrical response to Shh signaling in molar developmentM Nakatomi, M Hovorakova, A Gritli-Linde, et al.
British Heart Journal|October 1, 1991
DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal originD I Wilson, I E Cross, J A Goodship, et al.
American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.
Pageof 4