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Amanda Dixon-McIver

Showing results (1-10 of 11) with videos related to

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Translational Pediatrics|February 3, 2016
Emerging technologies in paediatric leukaemiaAmanda Dixon-McIver
Methods in Molecular Biology (Clifton, N.J.)|September 10, 2010
MicroRNA detection in bone marrow cells by LNA-FISHSilvana Debernardi, Amanda Dixon-McIver
Cancer Genetics|November 21, 2017
Detection of complex genomic signatures associated with risk in plasma cell disordersNadine K Berry, Amanda Dixon-McIver, Rodney J Scott, et al.
The New Zealand Medical Journal|June 21, 2022
Validation of a molecular assay to detect SARS-CoV-2 in salivaJanet L Pitman, Arthur J Morris, Stephen Grice, et al.
Plos One|May 15, 2008
Distinctive patterns of microRNA expression associated with karyotype in acute myeloid leukaemiaAmanda Dixon-McIver, Phil East, Charles A Mein, et al.
Applied Immunohistochemistry & Molecular Morphology : AIMM|February 11, 2016
NRASQ61R Mutation-specific Immunohistochemistry is Highly Specific for Either NRASQ61R or KRASQ61R Mutation in Colorectal CarcinomaJohn Turchini, Juliana Andrici, Loretta Sioson, et al.
Genes, Chromosomes & Cancer|March 28, 2003
Mutations of CEBPA in acute myeloid leukemia FAB types M1 and M2Jennifer Snaddon, Matthew L Smith, Michael Neat, et al.
Internal Medicine Journal|July 19, 2019
Screening for anaplastic lymphoma kinase (ALK) gene rearrangements in non-small-cell lung cancer in New ZealandMark J McKeage, Sandar Tin Tin, Prashannata Khwaounjoo, et al.
Journal of Medical Genetics|February 2, 2020
ATR-16 syndrome: mechanisms linking monosomy to phenotypeChristian Babbs, Jill Brown, Sharon W Horsley, et al.
Cancer Genetics|November 1, 2018
Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasmsRashmi Kanagal-Shamanna, Jennelle C Hodge, Tracy Tucker, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Translational Pediatrics|February 3, 2016
Emerging technologies in paediatric leukaemiaAmanda Dixon-McIver
Methods in Molecular Biology (Clifton, N.J.)|September 10, 2010
MicroRNA detection in bone marrow cells by LNA-FISHSilvana Debernardi, Amanda Dixon-McIver
Cancer Genetics|November 21, 2017
Detection of complex genomic signatures associated with risk in plasma cell disordersNadine K Berry, Amanda Dixon-McIver, Rodney J Scott, et al.
The New Zealand Medical Journal|June 21, 2022
Validation of a molecular assay to detect SARS-CoV-2 in salivaJanet L Pitman, Arthur J Morris, Stephen Grice, et al.
Plos One|May 15, 2008
Distinctive patterns of microRNA expression associated with karyotype in acute myeloid leukaemiaAmanda Dixon-McIver, Phil East, Charles A Mein, et al.
Applied Immunohistochemistry & Molecular Morphology : AIMM|February 11, 2016
NRASQ61R Mutation-specific Immunohistochemistry is Highly Specific for Either NRASQ61R or KRASQ61R Mutation in Colorectal CarcinomaJohn Turchini, Juliana Andrici, Loretta Sioson, et al.
Genes, Chromosomes & Cancer|March 28, 2003
Mutations of CEBPA in acute myeloid leukemia FAB types M1 and M2Jennifer Snaddon, Matthew L Smith, Michael Neat, et al.
Internal Medicine Journal|July 19, 2019
Screening for anaplastic lymphoma kinase (ALK) gene rearrangements in non-small-cell lung cancer in New ZealandMark J McKeage, Sandar Tin Tin, Prashannata Khwaounjoo, et al.
Journal of Medical Genetics|February 2, 2020
ATR-16 syndrome: mechanisms linking monosomy to phenotypeChristian Babbs, Jill Brown, Sharon W Horsley, et al.
Cancer Genetics|November 1, 2018
Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasmsRashmi Kanagal-Shamanna, Jennelle C Hodge, Tracy Tucker, et al.
Pageof 2