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D Benson

Showing results (331-340 of 721) with videos related to

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Scandinavian Journal of Immunology|June 1, 1995
In vitro degradation of serum amyloid A by cathepsin D and other acid proteases: possible protection against amyloid fibril formationT Yamada, B Kluve-Beckerman, J J Liepnieks, et al.
Arthritis and Rheumatism|July 1, 1976
Identity of a peritoneal fluid immunoglobulin light chain and the amyloid fibril in primary amyloidosisP J Block, M Skinner, M D Benson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 1, 1997
Chick ciliary ganglion neurons contain transcripts coding for acetylcholine receptor-associated protein at synapses (rapsyn)A L Burns, D Benson, M J Howard, et al.
Biochimica Et Biophysica Acta|March 28, 1977
Fractionation of primary amyloid fibrils. Characterization and chemical interaction of the subunitsJ B Lian, M Skinner, M D Benson, et al.
International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association|June 1, 1979
Serum amyloid protein SAA, C-reactive protein and lysozyme in leprosyM A Scheinberg, A Masuda, M D Benson, et al.
The Journal of School Health|October 1, 1977
Results of school screening for scoliosis in the San Juan Unified School District, Sacramento, CaliforniaV K Harlin, K D Benson, B Wade, et al.
Journal of Allied Health|September 11, 2017
Impact of Student Response Systems on Initial Learning and Retention of Course Content in Health Sciences StudentsJeryl D Benson, Kimberly A Szucs, Elizabeth D DeIuliis, et al.
Digestive Diseases and Sciences|February 1, 1988
Prolonged jaundice following ketoconazole-induced hepatic injuryG D Benson, P K Anderson, B Combes, et al.
Biochemical and Biophysical Research Communications|October 31, 1988
Variant apolipoprotein AI as a major constituent of a human hereditary amyloidW C Nichols, F E Dwulet, J Liepnieks, et al.
Ophthalmic Genetics|February 29, 2024
Novel heterozygous <i>PRPH2</i> variant identified in a patient with spinocerebellar ataxia type 14 and macular dystrophyTugche S Chen, Narin Sheri, David S Ehmann, et al.
Pageof 73

Showing results (331-340 of 721) with videos related to

Sort By:
Pageof 73
Scandinavian Journal of Immunology|June 1, 1995
In vitro degradation of serum amyloid A by cathepsin D and other acid proteases: possible protection against amyloid fibril formationT Yamada, B Kluve-Beckerman, J J Liepnieks, et al.
Arthritis and Rheumatism|July 1, 1976
Identity of a peritoneal fluid immunoglobulin light chain and the amyloid fibril in primary amyloidosisP J Block, M Skinner, M D Benson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 1, 1997
Chick ciliary ganglion neurons contain transcripts coding for acetylcholine receptor-associated protein at synapses (rapsyn)A L Burns, D Benson, M J Howard, et al.
Biochimica Et Biophysica Acta|March 28, 1977
Fractionation of primary amyloid fibrils. Characterization and chemical interaction of the subunitsJ B Lian, M Skinner, M D Benson, et al.
International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association|June 1, 1979
Serum amyloid protein SAA, C-reactive protein and lysozyme in leprosyM A Scheinberg, A Masuda, M D Benson, et al.
The Journal of School Health|October 1, 1977
Results of school screening for scoliosis in the San Juan Unified School District, Sacramento, CaliforniaV K Harlin, K D Benson, B Wade, et al.
Journal of Allied Health|September 11, 2017
Impact of Student Response Systems on Initial Learning and Retention of Course Content in Health Sciences StudentsJeryl D Benson, Kimberly A Szucs, Elizabeth D DeIuliis, et al.
Digestive Diseases and Sciences|February 1, 1988
Prolonged jaundice following ketoconazole-induced hepatic injuryG D Benson, P K Anderson, B Combes, et al.
Biochemical and Biophysical Research Communications|October 31, 1988
Variant apolipoprotein AI as a major constituent of a human hereditary amyloidW C Nichols, F E Dwulet, J Liepnieks, et al.
Ophthalmic Genetics|February 29, 2024
Novel heterozygous <i>PRPH2</i> variant identified in a patient with spinocerebellar ataxia type 14 and macular dystrophyTugche S Chen, Narin Sheri, David S Ehmann, et al.
Pageof 73