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

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The Journal of Pathology|September 15, 2006
Gene profiling of cathepsin K deficiency in atherogenesis: profibrotic but lipogenicS P M Lutgens, N Kisters, E Lutgens, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 16, 1999
Presenilin 2 deficiency causes a mild pulmonary phenotype and no changes in amyloid precursor protein processing but enhances the embryonic lethal phenotype of presenilin 1 deficiencyA Herreman, D Hartmann, W Annaert, et al.
American Journal of Physiology. Renal Physiology|March 25, 2011
Tubular proteinuria in mice and humans lacking the intrinsic lysosomal protein SCARB2/Limp-2M J Desmond, D Lee, S A Fraser, et al.
Circulation|December 21, 2005
Disruption of the cathepsin K gene reduces atherosclerosis progression and induces plaque fibrosis but accelerates macrophage foam cell formationE Lutgens, S P M Lutgens, B C G Faber, et al.
Journal of Inherited Metabolic Disease|March 16, 2013
Enzyme replacement therapy for alpha-mannosidosis: 12 months follow-up of a single centre, randomised, multiple dose studyL Borgwardt, C I Dali, J Fogh, 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.
The Journal of Pathology|September 15, 2006
Gene profiling of cathepsin K deficiency in atherogenesis: profibrotic but lipogenicS P M Lutgens, N Kisters, E Lutgens, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 16, 1999
Presenilin 2 deficiency causes a mild pulmonary phenotype and no changes in amyloid precursor protein processing but enhances the embryonic lethal phenotype of presenilin 1 deficiencyA Herreman, D Hartmann, W Annaert, et al.
American Journal of Physiology. Renal Physiology|March 25, 2011
Tubular proteinuria in mice and humans lacking the intrinsic lysosomal protein SCARB2/Limp-2M J Desmond, D Lee, S A Fraser, et al.
Circulation|December 21, 2005
Disruption of the cathepsin K gene reduces atherosclerosis progression and induces plaque fibrosis but accelerates macrophage foam cell formationE Lutgens, S P M Lutgens, B C G Faber, et al.
Journal of Inherited Metabolic Disease|March 16, 2013
Enzyme replacement therapy for alpha-mannosidosis: 12 months follow-up of a single centre, randomised, multiple dose studyL Borgwardt, C I Dali, J Fogh, et al.
Pageof 6