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Ian M Carr

Showing results (31-40 of 96) with videos related to

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Laboratory Investigation; a Journal of Technical Methods and Pathology|July 6, 2019
Cas9-based enrichment and single-molecule sequencing for precise characterization of genomic duplicationsChristopher M Watson, Laura A Crinnion, Sarah Hewitt, et al.
Nature Communications|December 2, 2020
Functionally impaired plasmacytoid dendritic cells and non-haematopoietic sources of type I interferon characterize human autoimmunityAntonios Psarras, Adewonuola Alase, Agne Antanaviciute, et al.
Pathogens (Basel, Switzerland)|December 2, 2014
Effects of EGFR Inhibitor on Helicobacter pylori Induced Gastric Epithelial Pathology in VivoJean E Crabtree, Anthony H T Jeremy, Cedric Duval, et al.
Bioinformatics (Oxford, England)|May 8, 2026
Utilization of Long-Read Sequencing for the Detection of Structural Rearrangements with AgileStructureCarolina Lascelles, Morag Raynor, Laura A Crinnion, et al.
The Journal of Molecular Diagnostics : JMD|September 5, 2017
Characterization and Genomic Localization of a SMAD4 Processed PseudogeneChristopher M Watson, Nick Camm, Laura A Crinnion, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|April 15, 2009
Ketohexokinase: expression and localization of the principal fructose-metabolizing enzymeChristine P Diggle, Michael Shires, Derek Leitch, et al.
Human Mutation|November 5, 2011
Identification of autosomal recessive disease loci using out-bred nuclear familiesIan M Carr, Christine P Diggle, Nader Touqan, et al.
Human Mutation|October 24, 2012
Autozygosity mapping with exome sequence dataIan M Carr, Sanjeev Bhaskar, James O'Sullivan, et al.
BMC Clinical Pathology|December 17, 2013
An observational study on the expression levels of MDM2 and MDMX proteins, and associated effects on P53 in a series of human liposarcomasNader Touqan, Christine P Diggle, Edlo T Verghese, et al.
BMC Neurology|December 2, 2004
Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disordersClare N Lynex, Ian M Carr, Jack P Leek, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 6, 2019
Cas9-based enrichment and single-molecule sequencing for precise characterization of genomic duplicationsChristopher M Watson, Laura A Crinnion, Sarah Hewitt, et al.
Nature Communications|December 2, 2020
Functionally impaired plasmacytoid dendritic cells and non-haematopoietic sources of type I interferon characterize human autoimmunityAntonios Psarras, Adewonuola Alase, Agne Antanaviciute, et al.
Pathogens (Basel, Switzerland)|December 2, 2014
Effects of EGFR Inhibitor on Helicobacter pylori Induced Gastric Epithelial Pathology in VivoJean E Crabtree, Anthony H T Jeremy, Cedric Duval, et al.
Bioinformatics (Oxford, England)|May 8, 2026
Utilization of Long-Read Sequencing for the Detection of Structural Rearrangements with AgileStructureCarolina Lascelles, Morag Raynor, Laura A Crinnion, et al.
The Journal of Molecular Diagnostics : JMD|September 5, 2017
Characterization and Genomic Localization of a SMAD4 Processed PseudogeneChristopher M Watson, Nick Camm, Laura A Crinnion, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|April 15, 2009
Ketohexokinase: expression and localization of the principal fructose-metabolizing enzymeChristine P Diggle, Michael Shires, Derek Leitch, et al.
Human Mutation|November 5, 2011
Identification of autosomal recessive disease loci using out-bred nuclear familiesIan M Carr, Christine P Diggle, Nader Touqan, et al.
Human Mutation|October 24, 2012
Autozygosity mapping with exome sequence dataIan M Carr, Sanjeev Bhaskar, James O'Sullivan, et al.
BMC Clinical Pathology|December 17, 2013
An observational study on the expression levels of MDM2 and MDMX proteins, and associated effects on P53 in a series of human liposarcomasNader Touqan, Christine P Diggle, Edlo T Verghese, et al.
BMC Neurology|December 2, 2004
Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disordersClare N Lynex, Ian M Carr, Jack P Leek, et al.
Pageof 10