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P Diggle

Showing results (111-120 of 150) with videos related to

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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 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.
Scientific Reports|January 13, 2015
Recombination is a key driver of genomic and phenotypic diversity in a Pseudomonas aeruginosa population during cystic fibrosis infectionSophie E Darch, Alan McNally, Freya Harrison, 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.
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.
International Journal of Molecular Sciences|August 12, 2018
Developing Hollow-Channel Gold Nanoflowers as Trimodal Intracellular NanoprobesSunjie Ye, May C Wheeler, James R McLaughlan, et al.
The American Journal of Pathology|July 24, 2003
Identification of genes up-regulated in urothelial tumors: the 67-kd laminin receptor and tumor-associated trypsin inhibitorChristine P Diggle, Sheena Cruickshank, Jonathon D Olsburgh, et al.
Physiological Genomics|September 16, 2010
Both isoforms of ketohexokinase are dispensable for normal growth and developmentC P Diggle, M Shires, C McRae, et al.
Health & Place|February 13, 2001
Analysing spatially referenced public health data: a comparison of three methodological approachesC E Dunn, S P Kingham, B Rowlingson, et al.
Genomics|May 31, 2011
Illuminator, a desktop program for mutation detection using short-read clonal sequencingIan M Carr, Joanne E Morgan, Christine P Diggle, et al.
Pageof 15

Showing results (111-120 of 150) with videos related to

Sort By:
Pageof 15
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 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.
Scientific Reports|January 13, 2015
Recombination is a key driver of genomic and phenotypic diversity in a Pseudomonas aeruginosa population during cystic fibrosis infectionSophie E Darch, Alan McNally, Freya Harrison, 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.
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.
International Journal of Molecular Sciences|August 12, 2018
Developing Hollow-Channel Gold Nanoflowers as Trimodal Intracellular NanoprobesSunjie Ye, May C Wheeler, James R McLaughlan, et al.
The American Journal of Pathology|July 24, 2003
Identification of genes up-regulated in urothelial tumors: the 67-kd laminin receptor and tumor-associated trypsin inhibitorChristine P Diggle, Sheena Cruickshank, Jonathon D Olsburgh, et al.
Physiological Genomics|September 16, 2010
Both isoforms of ketohexokinase are dispensable for normal growth and developmentC P Diggle, M Shires, C McRae, et al.
Health & Place|February 13, 2001
Analysing spatially referenced public health data: a comparison of three methodological approachesC E Dunn, S P Kingham, B Rowlingson, et al.
Genomics|May 31, 2011
Illuminator, a desktop program for mutation detection using short-read clonal sequencingIan M Carr, Joanne E Morgan, Christine P Diggle, et al.
Pageof 15