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W Edward Highsmith

Showing results (21-30 of 66) with videos related to

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Analytical Chemistry|February 14, 2004
DNA mutation detection in a polymer microfluidic network using temperature gradient gel electrophoresisJesse S Buch, Christopher Kimball, Frederick Rosenberger, et al.
Lab on a Chip|March 26, 2005
Denaturing gradient-based two-dimensional gene mutation scanning in a polymer microfluidic networkJesse S Buch, Frederick Rosenberger, W Edward Highsmith, et al.
Clinical Biochemistry|April 27, 2007
Comparison of three methods for genotyping the UGT1A1 (TA)n repeat polymorphismLinnea M Baudhuin, W Edward Highsmith, Jennifer Skierka, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Compound heterozygosity with a novel S222N GALT mutation leads to atypical galactosemia with loss of GALT activity in erythrocytes but little evidence of clinical diseaseBenjamin Cocanougher, Umut Aypar, Amber McDonald, et al.
The Journal of Molecular Diagnostics : JMD|April 29, 2005
Nine novel germline gene variants in the RET proto-oncogene identified in twelve unrelated casesSyed A Ahmed, Karen Snow-Bailey, W Edward Highsmith, et al.
Data in Brief|July 29, 2015
Biochemical and computational analyses of two phenotypically related GALT mutations (S222N and S135L) that lead to atypical galactosemiaBenjamin Cocanougher, Umut Aypar, Amber McDonald, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 4, 2013
Systemic transthyretin amyloidosis in a patient with bent spine syndromeKourosh Rezania, Peter Pytel, Laurel J Smit, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|September 27, 2002
Identifying and quantifying sources of variation in microarray data using high-density cDNA membrane arraysKevin R Coombes, W Edward Highsmith, Tammy A Krogmann, et al.
Mayo Clinic Proceedings|August 11, 2018
A Patient With Hereditary ATTR and a Novel AGel p.Ala578Pro AmyloidosisMeera Sridharan, W Edward Highsmith, Paul J Kurtin, et al.
The Journal of Molecular Diagnostics : JMD|January 26, 2007
Homozygous transthyretin mutation in an African American MaleEapen K Jacob, William D Edwards, Mark Zucker, et al.
Pageof 7

Showing results (21-30 of 66) with videos related to

Sort By:
Pageof 7
Analytical Chemistry|February 14, 2004
DNA mutation detection in a polymer microfluidic network using temperature gradient gel electrophoresisJesse S Buch, Christopher Kimball, Frederick Rosenberger, et al.
Lab on a Chip|March 26, 2005
Denaturing gradient-based two-dimensional gene mutation scanning in a polymer microfluidic networkJesse S Buch, Frederick Rosenberger, W Edward Highsmith, et al.
Clinical Biochemistry|April 27, 2007
Comparison of three methods for genotyping the UGT1A1 (TA)n repeat polymorphismLinnea M Baudhuin, W Edward Highsmith, Jennifer Skierka, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Compound heterozygosity with a novel S222N GALT mutation leads to atypical galactosemia with loss of GALT activity in erythrocytes but little evidence of clinical diseaseBenjamin Cocanougher, Umut Aypar, Amber McDonald, et al.
The Journal of Molecular Diagnostics : JMD|April 29, 2005
Nine novel germline gene variants in the RET proto-oncogene identified in twelve unrelated casesSyed A Ahmed, Karen Snow-Bailey, W Edward Highsmith, et al.
Data in Brief|July 29, 2015
Biochemical and computational analyses of two phenotypically related GALT mutations (S222N and S135L) that lead to atypical galactosemiaBenjamin Cocanougher, Umut Aypar, Amber McDonald, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 4, 2013
Systemic transthyretin amyloidosis in a patient with bent spine syndromeKourosh Rezania, Peter Pytel, Laurel J Smit, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|September 27, 2002
Identifying and quantifying sources of variation in microarray data using high-density cDNA membrane arraysKevin R Coombes, W Edward Highsmith, Tammy A Krogmann, et al.
Mayo Clinic Proceedings|August 11, 2018
A Patient With Hereditary ATTR and a Novel AGel p.Ala578Pro AmyloidosisMeera Sridharan, W Edward Highsmith, Paul J Kurtin, et al.
The Journal of Molecular Diagnostics : JMD|January 26, 2007
Homozygous transthyretin mutation in an African American MaleEapen K Jacob, William D Edwards, Mark Zucker, et al.
Pageof 7