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Showing results (51-60 of 55) with videos related to

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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.
Peptides|January 1, 1994
Isolation and characterization of a diuretic peptide common to the house fly and stable flyF L Clottens, G M Holman, G M Coast, 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 Biochemical Journal|July 6, 2001
Macrophage migration inhibitory factor of the parasitic nematode Trichinella spiralisT H Tan, S A Edgerton, R Kumari, 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.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
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.
Peptides|January 1, 1994
Isolation and characterization of a diuretic peptide common to the house fly and stable flyF L Clottens, G M Holman, G M Coast, 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 Biochemical Journal|July 6, 2001
Macrophage migration inhibitory factor of the parasitic nematode Trichinella spiralisT H Tan, S A Edgerton, R Kumari, 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.
Pageof 6