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W Edward Highsmith

Showing results (51-60 of 66) with videos related to

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Human Pathology|February 9, 2013
Molecular profiling of cholangiocarcinoma shows potential for targeted therapy treatment decisionsJesse S Voss, Leonard M Holtegaard, Sarah E Kerr, et al.
Clinical Chemistry|September 22, 2018
Applying Standard Clinical Chemistry Assay Validation to Droplet Digital PCR Quantitative Liquid Biopsy TestingDragana Milosevic, John R Mills, Michael B Campion, et al.
The Journal of Molecular Diagnostics : JMD|September 1, 2015
SERPINA1 Full-Gene Sequencing Identifies Rare Mutations Not Detected in Targeted Mutation AnalysisRondell P Graham, Michelle A Dina, Sarah C Howe, et al.
Head and Neck Pathology|September 8, 2019
First Report of Bilateral External Auditory Canal Cochlin Aggregates ("Cochlinomas") with Multifocal Amyloid-Like Deposits, Associated with Sensorineural Hearing Loss and a Novel Genetic Variant in COCH Encoding CochlinAtreyee Basu, Nicole J Boczek, Nahid G Robertson, et al.
Human Pathology|April 17, 2012
Isocitrate dehydrogenase 1 and 2 mutations in cholangiocarcinomaBenjamin R Kipp, Jesse S Voss, Sarah E Kerr, et al.
The Journal of Molecular Diagnostics : JMD|April 11, 2009
Development of genomic reference materials for cystic fibrosis genetic testingVictoria M Pratt, Michele Caggana, Christina Bridges, et al.
Mayo Clinic Proceedings|August 31, 2020
Amyloid Typing by Mass Spectrometry in Clinical Practice: a Comprehensive Review of 16,175 SamplesSurendra Dasari, Jason D Theis, Julie A Vrana, et al.
Investigative Ophthalmology & Visual Science|July 29, 2015
Trinucleotide Repeat Expansion in the TCF4 Gene in Fuchs' Endothelial Corneal Dystrophy in JapaneseMasakazu Nakano, Naoki Okumura, Hiroko Nakagawa, et al.
Journal of the American Society of Nephrology : JASN|June 15, 2016
Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CIISamih H Nasr, Surendra Dasari, Linda Hasadsri, et al.
Journal of the American Society of Nephrology : JASN|January 5, 2017
Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates with Unique PhenotypeSamih H Nasr, Surendra Dasari, John R Mills, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
Human Pathology|February 9, 2013
Molecular profiling of cholangiocarcinoma shows potential for targeted therapy treatment decisionsJesse S Voss, Leonard M Holtegaard, Sarah E Kerr, et al.
Clinical Chemistry|September 22, 2018
Applying Standard Clinical Chemistry Assay Validation to Droplet Digital PCR Quantitative Liquid Biopsy TestingDragana Milosevic, John R Mills, Michael B Campion, et al.
The Journal of Molecular Diagnostics : JMD|September 1, 2015
SERPINA1 Full-Gene Sequencing Identifies Rare Mutations Not Detected in Targeted Mutation AnalysisRondell P Graham, Michelle A Dina, Sarah C Howe, et al.
Head and Neck Pathology|September 8, 2019
First Report of Bilateral External Auditory Canal Cochlin Aggregates ("Cochlinomas") with Multifocal Amyloid-Like Deposits, Associated with Sensorineural Hearing Loss and a Novel Genetic Variant in COCH Encoding CochlinAtreyee Basu, Nicole J Boczek, Nahid G Robertson, et al.
Human Pathology|April 17, 2012
Isocitrate dehydrogenase 1 and 2 mutations in cholangiocarcinomaBenjamin R Kipp, Jesse S Voss, Sarah E Kerr, et al.
The Journal of Molecular Diagnostics : JMD|April 11, 2009
Development of genomic reference materials for cystic fibrosis genetic testingVictoria M Pratt, Michele Caggana, Christina Bridges, et al.
Mayo Clinic Proceedings|August 31, 2020
Amyloid Typing by Mass Spectrometry in Clinical Practice: a Comprehensive Review of 16,175 SamplesSurendra Dasari, Jason D Theis, Julie A Vrana, et al.
Investigative Ophthalmology & Visual Science|July 29, 2015
Trinucleotide Repeat Expansion in the TCF4 Gene in Fuchs' Endothelial Corneal Dystrophy in JapaneseMasakazu Nakano, Naoki Okumura, Hiroko Nakagawa, et al.
Journal of the American Society of Nephrology : JASN|June 15, 2016
Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CIISamih H Nasr, Surendra Dasari, Linda Hasadsri, et al.
Journal of the American Society of Nephrology : JASN|January 5, 2017
Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates with Unique PhenotypeSamih H Nasr, Surendra Dasari, John R Mills, et al.
Pageof 7