Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Dixon-McIver A"'
Autor:
Kanagal-Shamanna, Rashmi, Hodge, Jennelle C., Tucker, Tracy, Shetty, Shashi, Yenamandra, Ashwini, Dixon-McIver, Amanda, Bryke, Christine, Huxley, Emma, Lennon, Patrick A., Raca, Gordana, Xu, Xinjie, Jeffries, Sally, Quintero-Rivera, Fabiola, Greipp, Patricia T., Slovak, Marilyn L., Iqbal, M. Anwar, Fang, Min
Publikováno v:
In Cancer Genetics December 2018 228-229:197-217
Autor:
Xu, Xinjie, Bryke, Christine, Sukhanova, Madina, Huxley, Emma, Dash, D.P., Dixon-Mciver, Amanda, Fang, Min, Griepp, Patricia T., Hodge, Jennelle C., Iqbal, Anwar, Jeffries, Sally, Kanagal-Shamanna, Rashmi, Quintero-Rivera, Fabiola, Shetty, Shashi, Slovak, Marilyn L., Yenamandra, Ashwini, Lennon, Patrick A., Raca, Gordana
Publikováno v:
In Cancer Genetics December 2018 228-229:218-235
Autor:
Berry, Nadine K. *, Dixon-McIver, Amanda, Scott, Rodney J., Rowlings, Philip, Enjeti, Anoop K.
Publikováno v:
In Cancer Genetics December 2017 218-219:1-9
Publikováno v:
In Cancer Genetics November 2023 278-279 Supplement 1
Autor:
Janet L, Pitman, Arthur J, Morris, Stephen, Grice, Joseph T, Walsh, Leyi, Wang, Martin D, Burke, Amanda, Dixon-McIver
Publikováno v:
The New Zealand medical journal. 134(1547)
To validate a reverse transcriptase-quantitative polymerase chain reaction (RT-qPCR) assay to detect SARS-CoV-2 in saliva in two independent Aotearoa New Zealand laboratories.An RT-qPCR assay developed at University of Illinois Urbana-Champaign, USA,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::94aad1bcfb653f95a48ef7c8c06f0dbd
https://pubmed.ncbi.nlm.nih.gov/35728108
https://pubmed.ncbi.nlm.nih.gov/35728108
Autor:
Amanda Dixon-McIver, J. Traeger-Synodinos, Douglas R. Higgs, Shiwangini Kumar, Evie Maifoshie, Christian Babbs, Veronica J. Buckle, Paul Ooijevaar, Jill M. Brown, Cornelis L. Harteveld, Andrew O.M. Wilkie, Joanne Slater, Marjolein Kriek, Sharon W. Horsley
Publikováno v:
Journal of Medical Genetics, 57(6), 414-421. BMJ PUBLISHING GROUP
Journal of Medical Genetics
Journal of Medical Genetics
BackgroundDeletions removing 100s–1000s kb of DNA, and variable numbers of poorly characterised genes, are often found in patients with a wide range of developmental abnormalities. In such cases, understanding the contribution of the deletion to an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79ea1525605a7b60733ee8d057982dac
https://hdl.handle.net/1887/3184788
https://hdl.handle.net/1887/3184788
Background: Deletions removing 100s-1000s kb of DNA, and variable numbers of poorly characterised genes, are often found in patients with a wide range of developmental abnormalities. In such cases, understanding the contribution of the deletion to an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::5618fa09615104e4d0ac08e8ac8e8ffb
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078400
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078400
Autor:
Xinjie Xu, Emma Huxley, Sally Jeffries, Amanda Dixon-McIver, Min Fang, Tracy Tucker, Gordana Raca, Patrick A. Lennon, M. Anwar Iqbal, Marilyn L. Slovak, Patricia T. Greipp, Jennelle C. Hodge, Rashmi Kanagal-Shamanna, Ashwini Yenamandra, Fabiola Quintero-Rivera, Christine R. Bryke, Shashi Shetty
Publikováno v:
Cancer Genetics. :197-217
Multiple studies have demonstrated the utility of chromosomal microarray (CMA) testing to identify clinically significant copy number alterations (CNAs) and copy-neutral loss-of-heterozygosity (CN-LOH) in myeloid malignancies. However, guidelines for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51555608ccf5e376f0166d80fad4aad1
https://doi.org/10.1016/j.cancergen.2018.07.003
https://doi.org/10.1016/j.cancergen.2018.07.003
Autor:
Amanda Dixon-McIver, Phil East, Charles A Mein, Jean-Baptiste Cazier, Gael Molloy, Tracy Chaplin, T Andrew Lister, Bryan D Young, Silvana Debernardi
Publikováno v:
PLoS ONE, Vol 3, Iss 5, p e2141 (2008)
Acute myeloid leukaemia (AML) is the most common acute leukaemia in adults; however, the genetic aetiology of the disease is not yet fully understood. A quantitative expression profile analysis of 157 mature miRNAs was performed on 100 AML patients r
Externí odkaz:
https://doaj.org/article/18c2a0160e454ae58547d7a035fe6355
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