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J Goodship

Showing results (1-10 of 137) with videos related to

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Current Opinion in Genetics & Development|June 1, 1996
Developmental genetics of the heartJ Burn, J Goodship
Kidney International|July 1, 2006
Factor H genotype-phenotype correlations: lessons from aHUS, MPGN II, and AMDT H J Goodship
Current Opinion in Hematology|July 9, 2010
Atypical hemolytic uremic syndromeDavid Kavanagh, Timothy H J Goodship
Human Genetics|December 1, 1989
Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving maleJ Goodship, R Levinsky, S Malcolm
Seminars in Thrombosis and Hemostasis|April 1, 2006
Membrane cofactor protein and factor I: mutations and transplantationDavid Kavanagh, Timothy H J Goodship
American Journal of Medical Genetics|January 22, 1996
X-inactivation patterns in monozygotic and dizygotic female twinsJ Goodship, J Carter, J Burn
Hematology. American Society of Hematology. Education Program|December 14, 2011
Atypical hemolytic uremic syndrome, genetic basis, and clinical manifestationsDavid Kavanagh, Timothy H J Goodship
Journal of Molecular Biology|February 20, 2002
Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding siteStephen J Perkins, Timothy H J Goodship
The Journal of Experimental Medicine|June 6, 2007
Complement factor H and the hemolytic uremic syndromeJohn P Atkinson, Timothy H J Goodship
Clinical and Experimental Immunology|January 1, 1991
Evidence that X-linked severe combined immunodeficiency is not a differentiation defect of T lymphocytesJ Goodship, S Malcolm, R J Levinsky
Pageof 14

Showing results (1-10 of 137) with videos related to

Sort By:
Pageof 14
Current Opinion in Genetics & Development|June 1, 1996
Developmental genetics of the heartJ Burn, J Goodship
Kidney International|July 1, 2006
Factor H genotype-phenotype correlations: lessons from aHUS, MPGN II, and AMDT H J Goodship
Current Opinion in Hematology|July 9, 2010
Atypical hemolytic uremic syndromeDavid Kavanagh, Timothy H J Goodship
Human Genetics|December 1, 1989
Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving maleJ Goodship, R Levinsky, S Malcolm
Seminars in Thrombosis and Hemostasis|April 1, 2006
Membrane cofactor protein and factor I: mutations and transplantationDavid Kavanagh, Timothy H J Goodship
American Journal of Medical Genetics|January 22, 1996
X-inactivation patterns in monozygotic and dizygotic female twinsJ Goodship, J Carter, J Burn
Hematology. American Society of Hematology. Education Program|December 14, 2011
Atypical hemolytic uremic syndrome, genetic basis, and clinical manifestationsDavid Kavanagh, Timothy H J Goodship
Journal of Molecular Biology|February 20, 2002
Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding siteStephen J Perkins, Timothy H J Goodship
The Journal of Experimental Medicine|June 6, 2007
Complement factor H and the hemolytic uremic syndromeJohn P Atkinson, Timothy H J Goodship
Clinical and Experimental Immunology|January 1, 1991
Evidence that X-linked severe combined immunodeficiency is not a differentiation defect of T lymphocytesJ Goodship, S Malcolm, R J Levinsky
Pageof 14