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Jacob D Durtschi

Showing results (11-20 of 22) with videos related to

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Clinical Chemistry|November 6, 2007
Quadruplex genotyping of F5, F2, and MTHFR variants in a single closed tube by high-resolution amplicon meltingMichael T Seipp, David Pattison, Jacob D Durtschi, et al.
Clinical Chemistry|June 12, 2004
Extraction and amplification of genomic DNA from human blood on nanoporous aluminum oxide membranesMarc G Elgort, Mark G Herrmann, Maria Erali, et al.
Journal of Biomolecular Techniques : JBT|July 9, 2011
Variant identification in multi-sample pools by illumina genome analyzer sequencingRebecca L Margraf, Jacob D Durtschi, Shale Dames, et al.
Journal of Biomolecular Techniques : JBT|September 3, 2010
Multi-sample pooling and illumina genome analyzer sequencing methods to determine gene sequence variation for database developmentRebecca L Margraf, Jacob D Durtschi, Shale Dames, et al.
Clinical Immunology (Orlando, Fla.)|November 21, 2012
TACI mutation p.Lys154Ter identified in Good SyndromeRebecca L Margraf, Emily M Coonrod, Jacob D Durtschi, et al.
Journal of Medical Microbiology|August 11, 2005
Increased sensitivity of bacterial detection in cerebrospinal fluid by fluorescent staining on low-fluorescence membrane filtersJacob D Durtschi, Maria Erali, L Kathryn Bromley, et al.
The Journal of Molecular Diagnostics : JMD|June 27, 2007
Unlabeled oligonucleotides as internal temperature controls for genotyping by amplicon meltingMichael T Seipp, Jacob D Durtschi, Michael A Liew, et al.
BMC Medical Genomics|November 15, 2012
A direct comparison of next generation sequencing enrichment methods using an aortopathy gene panel- clinical diagnostics perspectiveWhitney L Wooderchak-Donahue, Brendan O'Fallon, Larissa V Furtado, et al.
Journal of Clinical Immunology|December 18, 2014
Identification of patients with RAG mutations previously diagnosed with common variable immunodeficiency disordersDavid Buchbinder, Rebecca Baker, Yu Nee Lee, et al.
American Journal of Human Genetics|October 22, 2013
Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiencyKarin Chen, Emily M Coonrod, Attila Kumánovics, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Clinical Chemistry|November 6, 2007
Quadruplex genotyping of F5, F2, and MTHFR variants in a single closed tube by high-resolution amplicon meltingMichael T Seipp, David Pattison, Jacob D Durtschi, et al.
Clinical Chemistry|June 12, 2004
Extraction and amplification of genomic DNA from human blood on nanoporous aluminum oxide membranesMarc G Elgort, Mark G Herrmann, Maria Erali, et al.
Journal of Biomolecular Techniques : JBT|July 9, 2011
Variant identification in multi-sample pools by illumina genome analyzer sequencingRebecca L Margraf, Jacob D Durtschi, Shale Dames, et al.
Journal of Biomolecular Techniques : JBT|September 3, 2010
Multi-sample pooling and illumina genome analyzer sequencing methods to determine gene sequence variation for database developmentRebecca L Margraf, Jacob D Durtschi, Shale Dames, et al.
Clinical Immunology (Orlando, Fla.)|November 21, 2012
TACI mutation p.Lys154Ter identified in Good SyndromeRebecca L Margraf, Emily M Coonrod, Jacob D Durtschi, et al.
Journal of Medical Microbiology|August 11, 2005
Increased sensitivity of bacterial detection in cerebrospinal fluid by fluorescent staining on low-fluorescence membrane filtersJacob D Durtschi, Maria Erali, L Kathryn Bromley, et al.
The Journal of Molecular Diagnostics : JMD|June 27, 2007
Unlabeled oligonucleotides as internal temperature controls for genotyping by amplicon meltingMichael T Seipp, Jacob D Durtschi, Michael A Liew, et al.
BMC Medical Genomics|November 15, 2012
A direct comparison of next generation sequencing enrichment methods using an aortopathy gene panel- clinical diagnostics perspectiveWhitney L Wooderchak-Donahue, Brendan O'Fallon, Larissa V Furtado, et al.
Journal of Clinical Immunology|December 18, 2014
Identification of patients with RAG mutations previously diagnosed with common variable immunodeficiency disordersDavid Buchbinder, Rebecca Baker, Yu Nee Lee, et al.
American Journal of Human Genetics|October 22, 2013
Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiencyKarin Chen, Emily M Coonrod, Attila Kumánovics, et al.
Pageof 3