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Susan L. Heatley

Researcher at University of Adelaide

Publications -  62
Citations -  4746

Susan L. Heatley is an academic researcher from University of Adelaide. The author has contributed to research in topics: Gene & Transplantation. The author has an hindex of 22, co-authored 55 publications receiving 4294 citations. Previous affiliations of Susan L. Heatley include Australian Red Cross & Australian Red Cross Blood Service.

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Journal ArticleDOI

The genetic basis of early T-cell precursor acute lymphoblastic leukaemia

Jinghui Zhang, +73 more
- 12 Jan 2012 - 
TL;DR: The mutational spectrum is similar to myeloid tumours, and moreover, the global transcriptional profile of ETP ALL was similar to that of normal andMyeloid leukaemia haematopoietic stem cells, suggesting that addition of myeloids-directed therapies might improve the poor outcome of E TP ALL.
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The genomic landscape of hypodiploid acute lymphoblastic leukemia

TL;DR: Both near-haploid and low-hypodiploid leukemic cells show activation of Ras-signaling and phosphoinositide 3-kinase (PI3K)-signaling pathways and are sensitive to PI3K inhibitors, indicating that these drugs should be explored as a new therapeutic strategy for this aggressive form of leukemia.
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CREBBP mutations in relapsed acute lymphoblastic leukaemia

TL;DR: Analysis of an extended cohort of 71 diagnosis–relapse cases and 270 acute leukaemia cases that did not relapse found that 18.3% of relapse cases had sequence or deletion mutations of CREBBP, which encodes the transcriptional coactivator and histone acetyltransferase CREB-binding protein (CREBBP).
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CREST maps somatic structural variation in cancer genomes with base-pair resolution

TL;DR: Application of CREST to whole-genome sequencing data from five pediatric T-lineage acute lymphoblastic leukemias and a human melanoma cell line, COLO-829, identified 160 somatic structural variations.
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Analysis of the relationship between mannose-binding lectin (MBL) genotype, MBL levels and function in an Australian blood donor population.

TL;DR: Comprehensive MBL genotyping and functional MBL quantitation using mannan‐binding and C4‐deposition assays have the potential to be highly informative in MBL disease association studies.