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M Morison

Showing results (71-80 of 114) with videos related to

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Journal of Biomedicine & Biotechnology|November 30, 2012
Technical considerations for reduced representation bisulfite sequencing with multiplexed librariesAniruddha Chatterjee, Euan J Rodger, Peter A Stockwell, et al.
Plos One|June 19, 2015
Interspecies Variation in the Functional Consequences of Mutation of Cytochrome cTracy M Josephs, Moira E Hibbs, Lily Ong, et al.
Human Mutation|April 5, 2002
A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362XRosemary W Heathcott, Ian M Morison, Marie Claire Gubler, et al.
British Journal of Haematology|April 21, 2015
Green neutrophil and monocyte inclusions - time to acknowledge and reportTimothy O Hodgson, Anna Ruskova, Clare J Shugg, et al.
Nature Medicine|March 1, 1996
Somatic overgrowth associated with overexpression of insulin-like growth factor III M Morison, D M Becroft, T Taniguchi, et al.
Environmental Pollution (Barking, Essex : 1987)|November 10, 2018
DNA methylation and gene expression alterations in zebrafish early-life stages exposed to the antibacterial agent triclosanElodie Falisse, Bertrand Ducos, Peter A Stockwell, et al.
Oncogene|January 13, 2009
Canonical WNT signalling determines lineage specificity in Wilms tumourR Fukuzawa, M R Anaka, R J Weeks, et al.
Journal of Medical Genetics|February 25, 1998
Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth?K Okamoto, I M Morison, A E Reeve, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 3, 2004
Myogenesis in Wilms' tumors is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathwayRyuji Fukuzawa, Rosemary W Heathcott, Makoto Sano, et al.
The Biochemical Journal|December 17, 2013
Enhancing the peroxidase activity of cytochrome c by mutation of residue 41: implications for the peroxidase mechanism and cytochrome c releaseTracy M Josephs, Ian M Morison, Catherine L Day, et al.
Pageof 12

Showing results (71-80 of 114) with videos related to

Sort By:
Pageof 12
Journal of Biomedicine & Biotechnology|November 30, 2012
Technical considerations for reduced representation bisulfite sequencing with multiplexed librariesAniruddha Chatterjee, Euan J Rodger, Peter A Stockwell, et al.
Plos One|June 19, 2015
Interspecies Variation in the Functional Consequences of Mutation of Cytochrome cTracy M Josephs, Moira E Hibbs, Lily Ong, et al.
Human Mutation|April 5, 2002
A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362XRosemary W Heathcott, Ian M Morison, Marie Claire Gubler, et al.
British Journal of Haematology|April 21, 2015
Green neutrophil and monocyte inclusions - time to acknowledge and reportTimothy O Hodgson, Anna Ruskova, Clare J Shugg, et al.
Nature Medicine|March 1, 1996
Somatic overgrowth associated with overexpression of insulin-like growth factor III M Morison, D M Becroft, T Taniguchi, et al.
Environmental Pollution (Barking, Essex : 1987)|November 10, 2018
DNA methylation and gene expression alterations in zebrafish early-life stages exposed to the antibacterial agent triclosanElodie Falisse, Bertrand Ducos, Peter A Stockwell, et al.
Oncogene|January 13, 2009
Canonical WNT signalling determines lineage specificity in Wilms tumourR Fukuzawa, M R Anaka, R J Weeks, et al.
Journal of Medical Genetics|February 25, 1998
Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth?K Okamoto, I M Morison, A E Reeve, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 3, 2004
Myogenesis in Wilms' tumors is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathwayRyuji Fukuzawa, Rosemary W Heathcott, Makoto Sano, et al.
The Biochemical Journal|December 17, 2013
Enhancing the peroxidase activity of cytochrome c by mutation of residue 41: implications for the peroxidase mechanism and cytochrome c releaseTracy M Josephs, Ian M Morison, Catherine L Day, et al.
Pageof 12