D Catchpoole
D Catchpoole
Head, Tumour Bank, The Children's Hospital at Westmead
Verifierad e-postadress på health.nsw.gov.au
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Comprehensive genomic analysis of rhabdomyosarcoma reveals a landscape of alterations affecting a common genetic axis in fusion-positive and fusion-negative tumors
JF Shern, L Chen, J Chmielecki, JS Wei, R Patidar, M Rosenberg, ...
Cancer discovery 4 (2), 216-231, 2014
3622014
Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models
JGT Vi, AT Cheuk, PS Tsang, JY Chung, YK Song, K Desai, Y Yu, ...
The Journal of clinical investigation 119 (11), 3395-3407, 2009
2682009
The genomic landscape of the Ewing sarcoma family of tumors reveals recurrent STAG2 mutation
A Brohl, D Solomon, W Chang, J Wang, Y Song, S Sandiri, R Patidar, ...
PLoS Genetics 10 (7), e1004475, 2014
2602014
The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias
AK Andersson, J Ma, J Wang, X Chen, AL Gedman, J Dang, J Nakitandwe, ...
Nature genetics 47 (4), 330-337, 2015
2462015
Prediction of clinical outcome using gene expression profiling and artificial neural networks for patients with neuroblastoma
JS Wei, BT Greer, F Westermann, SM Steinberg, CG Son, QR Chen, ...
Cancer research 64 (19), 6883-6891, 2004
2312004
Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour
D Astuti, F Latif, K Wagner, D Gentle, WN Cooper, D Catchpoole, ...
British journal of cancer 92 (8), 1574-1580, 2005
1432005
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
KW Brown, AJ Villar, W Bickmore, J Clayton-Smith, D Catchpoole, ...
Human molecular genetics 5 (12), 2027-2032, 1996
1351996
Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome
JA Joyce, WK Lam, DJ Catchpoole, P Jenks, W Reik, ER Maher, ...
Human molecular genetics 6 (9), 1543-1548, 1997
1331997
High-resolution analysis of chromosomal breakpoints and genomic instability identifies PTPRD as a candidate tumor suppressor gene in neuroblastoma
RL Stallings, P Nair, JM Maris, D Catchpoole, M McDermott, A O'Meara, ...
Cancer research 66 (7), 3673-3680, 2006
1302006
The novel RASSF6 and RASSF10 candidate tumour suppressor genes are frequently epigenetically inactivated in childhood leukaemias
LB Hesson, TL Dunwell, WN Cooper, D Catchpoole, AT Brini, ...
Molecular cancer 8 (1), 42, 2009
1142009
Credentialing preclinical pediatric xenograft models using gene expression and tissue microarray analysis
CC Whiteford, S Bilke, BT Greer, Q Chen, TA Braunschweig, N Cenacchi, ...
Cancer research 67 (1), 32-40, 2007
1122007
A genome-wide screen identifies frequently methylated genes in haematological and epithelial cancers
T Dunwell, L Hesson, TA Rauch, L Wang, RE Clark, A Dallol, D Gentle, ...
Molecular cancer 9 (1), 44, 2010
1062010
Epigenetic analysis of childhood acute lymphoblastic leukemia
TL Dunwell, LB Hesson, TV Pavlova, V Zabarovska, VI Kashuba, ...
Epigenetics 4 (3), 185-193, 2009
1042009
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.
D Catchpoole, WW Lam, D Valler, IK Temple, JA Joyce, W Reik, ...
Journal of medical genetics 34 (5), 353-359, 1997
1011997
Integrated (epi)-genomic analyses identify subgroup-specific therapeutic targets in CNS rhabdoid tumors
J Torchia, B Golbourn, S Feng, KC Ho, P Sin-Chan, A Vasiljevic, ...
Cancer cell 30 (6), 891-908, 2016
992016
cDNA array-CGH profiling identifies genomic alterations specific to stage and MYCN-amplification in neuroblastoma
QR Chen, S Bilke, JS Wei, CC Whiteford, N Cenacchi, AL Krasnoselsky, ...
BMC genomics 5 (1), 70, 2004
962004
Etoposide-induced cytotoxicity in two human T-cell leukemic lines: delayed loss of membrane permeability rather than DNA fragmentation as an indicator of programmed cell death
DR Catchpoole, BW Stewart
Cancer research 53 (18), 4287-4296, 1993
931993
Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DCR1, DCR2, DR4, DR5, KvDMR1, H19 and preferential 11p15. 5 maternal-allele loss in von Hippel-Lindau and sporadic …
CDE Margetts, D Astuti, DC Gentle, WN Cooper, A Cascon, D Catchpoole, ...
Endocrine-Related Cancer 12 (1), 161-172, 2005
922005
Oligonucleotide microarray analysis of gene expression in neuroblastoma displaying loss of chromosome 11q
L McArdle, M McDermott, R Purcell, D Grehan, A O'meara, F Breatnach, ...
Carcinogenesis 25 (9), 1599-1609, 2004
752004
The genetic basis and cell of origin of mixed phenotype acute leukaemia
TB Alexander, Z Gu, I Iacobucci, K Dickerson, JK Choi, B Xu, ...
Nature 562 (7727), 373-379, 2018
722018
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