Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Hongdo Do"'
Autor:
Anna deFazio, David D.L. Bowtell, Paul R. Harnett, Christine L. Clarke, Hongdo Do, Stephen Q. Wong, Alexander Dobrovic, Ian Campbell, Sally M. Hunter, Emanuele Palescandolo, Laura MacConaill, Rosemary Balleine, Alison Brand, Gerard V. Wain, Russell Hogg, Laura Galletta, Jillian Hung, Sian Fereday, Catherine Kennedy, Peter Russell, Raghwa Sharma, Michael S. Anglesio, Dariush Etemadmoghadam, Joshy George, Yoke-Eng Chiew, Catherine Emmanuel
Supplementary Methods, Figures 1-5. Supplementary Figure 1. Outline of cohort selection. Supplementary Figure 2. Example of whole-genome single-nucleotide polymorphism (SNP)array profile and genome alteration print (GAP). Supplementary Figure 3. Pre-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f8014a13412063debe453311afe9681
https://doi.org/10.1158/1078-0432.22458953.v1
https://doi.org/10.1158/1078-0432.22458953.v1
Autor:
Anna deFazio, David D.L. Bowtell, Paul R. Harnett, Christine L. Clarke, Hongdo Do, Stephen Q. Wong, Alexander Dobrovic, Ian Campbell, Sally M. Hunter, Emanuele Palescandolo, Laura MacConaill, Rosemary Balleine, Alison Brand, Gerard V. Wain, Russell Hogg, Laura Galletta, Jillian Hung, Sian Fereday, Catherine Kennedy, Peter Russell, Raghwa Sharma, Michael S. Anglesio, Dariush Etemadmoghadam, Joshy George, Yoke-Eng Chiew, Catherine Emmanuel
Supplementary Highlighted Methods. This document contains the revised supplementary methods and results with changes highlighted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a136b477838db3d8f47d1ece163bf4db
https://doi.org/10.1158/1078-0432.22458956
https://doi.org/10.1158/1078-0432.22458956
Autor:
Anna deFazio, David D.L. Bowtell, Paul R. Harnett, Christine L. Clarke, Hongdo Do, Stephen Q. Wong, Alexander Dobrovic, Ian Campbell, Sally M. Hunter, Emanuele Palescandolo, Laura MacConaill, Rosemary Balleine, Alison Brand, Gerard V. Wain, Russell Hogg, Laura Galletta, Jillian Hung, Sian Fereday, Catherine Kennedy, Peter Russell, Raghwa Sharma, Michael S. Anglesio, Dariush Etemadmoghadam, Joshy George, Yoke-Eng Chiew, Catherine Emmanuel
Supplementary Tables 1-7. Supplementary Table 1. SBT-EOC cases used for molecular analyses Supplementary Table 2. Mutations Screened on the Sequenom/OncoMap3 Platform Supplementary Table 3. Primer sequences for the indicated exons of TP53, ERBB2 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bf69e6f4d40820c503b1015b71fe4d0
https://doi.org/10.1158/1078-0432.22458950.v1
https://doi.org/10.1158/1078-0432.22458950.v1
Autor:
Anna deFazio, David D.L. Bowtell, Paul R. Harnett, Christine L. Clarke, Hongdo Do, Stephen Q. Wong, Alexander Dobrovic, Ian Campbell, Sally M. Hunter, Emanuele Palescandolo, Laura MacConaill, Rosemary Balleine, Alison Brand, Gerard V. Wain, Russell Hogg, Laura Galletta, Jillian Hung, Sian Fereday, Catherine Kennedy, Peter Russell, Raghwa Sharma, Michael S. Anglesio, Dariush Etemadmoghadam, Joshy George, Yoke-Eng Chiew, Catherine Emmanuel
Purpose: Low-grade serous ovarian carcinomas (LGSC) are Ras pathway-mutated, TP53 wild-type, and frequently associated with borderline tumors. Patients with LGSCs respond poorly to platinum-based chemotherapy and may benefit from pathway-targeted age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::242829df5029cd572e298c1f3d1c40f4
https://doi.org/10.1158/1078-0432.c.6524093.v1
https://doi.org/10.1158/1078-0432.c.6524093.v1
Autor:
Clare Senko, Trishe Leong, Paul Mitchell, Gareth Rivalland, Alexander Dobrovic, Chai Zi Quing, Geoffrey David Peters, Khashayar Asadi, Bibhusal Thapa, Hongdo Do, Marcin Szaumkessel, Thomas John, Jose Luis Leal
Publikováno v:
Lung Cancer. 146:154-159
Objectives Gene rearrangements involving NTRK1, NTRK2, NTRK3, ROS1 and ALK have been identified in many types of cancer, including non-small cell lung cancer (NSCLC). Data in malignant pleural mesothelioma (MPM), lung neuroendocrine tumors (NETs) and
Autor:
Gareth Rivalland, Eddie Lau, Paul Mitchell, Alexander Dobrovic, Ashan Musafer, Zoe Loh, Surein Arulananda, Hongdo Do, Thomas John
Publikováno v:
Journal of Thoracic Disease. 11:1756-1764
Background: Leptomeningeal spread in non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor ( EGFR ) mutations who experience disease progression on TKIs portends a poor prognosis. Mutation profiling of tumour DNA in cerebr
Autor:
Suzanne Allan, Rochelle C.J. D’Souza, S. Campbell, Hongdo Do, Kate Goasdoué, Peter Lucas, Alexander Dobrovic, Po Inglis, Zara C. Bruce, Gert Tollesson, Craig Winter, Andrew W. Boyd, Paul R. Jamieson, Carolin Offenhäuser, Rosalind L. Jeffree, Bryan W. Day, Seckin Akgul, Kathleen S. Ensbey, Brett W. Stringer, Thomas Robertson, Terrance Grant Johns, Yi Chieh Lim
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Scientific Reports
Scientific Reports
Low-passage, serum-free cell lines cultured from patient tumour tissue are the gold-standard for preclinical studies and cellular investigations of glioblastoma (GBM) biology, yet entrenched, poorly-representative cell line models are still widely us
Autor:
Daniel R A Cox, Boris Ka Leong Wong, Su Kah Goh, Alexander Dobrovic, Hongdo Do, Tom Witkowski, Ashan Musafer, Vijayaragavan Muralidharan
Publikováno v:
Clinical chemistry. 67(9)
Background Despite improvements in the genetic and epigenetic analysis of cell-free DNA (cfDNA), there has been limited focus on assessing the preanalytical variables of recovery efficiency following cfDNA extraction and bisulfite modification. Quant
Autor:
Greta Gillies, AS Harvey, Amy L Schneider, Alexander Dobrovic, William Maixner, John A. Damiano, Martin Wood, Paul J. Lockhart, Hongdo Do, Samuel F. Berkovic, Wei Shern Lee, Richard J. Leventer, Michael S. Hildebrand, Zac Chatterton, Jahnvi Pflueger, Ingrid E. Scheffer, Ryan Lister, Lara McQuillan, Kate Pope, Melanie Bahlo, Michael Wilson, Stephen M. Malone, Zimeng Ye, Bernadette Nolan
Publikováno v:
Brain Communications
Brain somatic mutations are an increasingly recognized cause of epilepsy, brain malformations and autism spectrum disorders and may be a hidden cause of other neurodevelopmental and neurodegenerative disorders. At present, brain mosaicism can be dete
Autor:
Rosemary Burgess, John A. Damiano, Samuel F. Berkovic, Michael S. Hildebrand, Alexander Dobrovic, Renate M Kalnins, Ezgi Ozturk, Hongdo Do, Nigel C. Jones
Publikováno v:
Epileptic Disorders. 19:450-455
Somatic mutation of the lissencephaly-1 gene is a cause of subcortical band heterotopia ("double cortex"). The severity of the phenotype depends on the level of mutation in brain tissue. Detecting and quantifying low-level somatic mosaic mutations is