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Showing results (81-90 of 86) with videos related to

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Biochemical and Biophysical Research Communications|December 30, 1994
Heart fatty acid binding protein is a novel regulator of cardiac myocyte hypertrophyP B Burton, C E Hogben, C L Joannou, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 1992
Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosisA K Soutar, P N Hawkins, D M Vigushin, et al.
QJM : Monthly Journal of the Association of Physicians|October 1, 1995
A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosisD R Booth, S Y Tan, S E Booth, et al.
European Journal of Immunology|December 23, 1998
The gp200-MR6 molecule which is functionally associated with the IL-4 receptor modulates B cell phenotype and is a novel member of the human macrophage mannose receptor familyP F McKay, N Imami, M Johns, et al.
The Journal of Clinical Investigation|June 15, 1996
Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI geneD R Booth, S Y Tan, S E Booth, et al.
Kidney International|September 11, 2014
The urinary proteome and metabonome differ from normal in adults with mitochondrial diseaseAndrew M Hall, Annalisa Vilasi, Isabel Garcia-Perez, et al.
Pageof 9

Showing results (81-90 of 86) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 86 results.
Biochemical and Biophysical Research Communications|December 30, 1994
Heart fatty acid binding protein is a novel regulator of cardiac myocyte hypertrophyP B Burton, C E Hogben, C L Joannou, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 1992
Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosisA K Soutar, P N Hawkins, D M Vigushin, et al.
QJM : Monthly Journal of the Association of Physicians|October 1, 1995
A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosisD R Booth, S Y Tan, S E Booth, et al.
European Journal of Immunology|December 23, 1998
The gp200-MR6 molecule which is functionally associated with the IL-4 receptor modulates B cell phenotype and is a novel member of the human macrophage mannose receptor familyP F McKay, N Imami, M Johns, et al.
The Journal of Clinical Investigation|June 15, 1996
Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI geneD R Booth, S Y Tan, S E Booth, et al.
Kidney International|September 11, 2014
The urinary proteome and metabonome differ from normal in adults with mitochondrial diseaseAndrew M Hall, Annalisa Vilasi, Isabel Garcia-Perez, et al.
Pageof 9