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D Benson

Showing results (621-630 of 721) with videos related to

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The American Journal of Pathology|January 23, 1999
Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1L Hamidi Asl, J J Liepnieks, K Hamidi Asl, et al.
Human Genetics|September 1, 1995
Haplotype analysis of common transthyretin mutationsM R Almeida, N Aoyama-Oishi, Y Sakaki, et al.
The Journal of Biological Chemistry|February 9, 2019
A pair of peptides inhibits seeding of the hormone transporter transthyretin into amyloid fibrilsLorena Saelices, Binh A Nguyen, Kevin Chung, et al.
Agents and Actions. Supplements|January 1, 1985
Effects of Voltaren on arachidonic acid metabolism in arthritis patientsH L Liauw, E Ku, K D Brandt, et al.
Biochimica Et Biophysica Acta|June 4, 1999
Identification of a novel substitution in the constant region of a gene coding for an amyloidogenic kappa1 light chainJ Wally, G Kica, Y Zhang, et al.
The Journal of Clinical Investigation|December 1, 1990
A point mutation in transthyretin increases affinity for thyroxine and produces euthyroid hyperthyroxinemiaA C Moses, H N Rosen, D E Moller, et al.
Neurology|September 25, 2003
Amyloidoma of a spinal rootS McKechnie, F Yang, C G Harper, et al.
Journal of the Neurological Sciences|July 12, 2014
Retrospective study of a TTR FAP cohort to modify NIS+7 for therapeutic trialsN Suanprasert, J L Berk, M D Benson, et al.
Ophthalmic Genetics|September 25, 2020
Severe retinal degeneration in a patient with Canavan diseaseMatthew D Benson, David J A Plemel, Paul R Freund, et al.
Lancet (London, England)|September 18, 1993
Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseasesA M Saunders, K Schmader, J C Breitner, et al.
Pageof 73

Showing results (621-630 of 721) with videos related to

Sort By:
Pageof 73
The American Journal of Pathology|January 23, 1999
Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1L Hamidi Asl, J J Liepnieks, K Hamidi Asl, et al.
Human Genetics|September 1, 1995
Haplotype analysis of common transthyretin mutationsM R Almeida, N Aoyama-Oishi, Y Sakaki, et al.
The Journal of Biological Chemistry|February 9, 2019
A pair of peptides inhibits seeding of the hormone transporter transthyretin into amyloid fibrilsLorena Saelices, Binh A Nguyen, Kevin Chung, et al.
Agents and Actions. Supplements|January 1, 1985
Effects of Voltaren on arachidonic acid metabolism in arthritis patientsH L Liauw, E Ku, K D Brandt, et al.
Biochimica Et Biophysica Acta|June 4, 1999
Identification of a novel substitution in the constant region of a gene coding for an amyloidogenic kappa1 light chainJ Wally, G Kica, Y Zhang, et al.
The Journal of Clinical Investigation|December 1, 1990
A point mutation in transthyretin increases affinity for thyroxine and produces euthyroid hyperthyroxinemiaA C Moses, H N Rosen, D E Moller, et al.
Neurology|September 25, 2003
Amyloidoma of a spinal rootS McKechnie, F Yang, C G Harper, et al.
Journal of the Neurological Sciences|July 12, 2014
Retrospective study of a TTR FAP cohort to modify NIS+7 for therapeutic trialsN Suanprasert, J L Berk, M D Benson, et al.
Ophthalmic Genetics|September 25, 2020
Severe retinal degeneration in a patient with Canavan diseaseMatthew D Benson, David J A Plemel, Paul R Freund, et al.
Lancet (London, England)|September 18, 1993
Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseasesA M Saunders, K Schmader, J C Breitner, et al.
Pageof 73