1. Adelaide Research & Scholarship

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Results 11-20 of 21 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2008AIRE'S CARD revealed, a new structure for the central tolerance provokes transcriptional plasticityFerguson, B.; Alexander, C.; Rossi, S.; Liiv, I.; Rebane, A.; Worth, C.; Wong, J.; Laan, M.; Peterson, P.; Jenkinson, E.; Anderson, G.; Scott, H.; Cooke, A.; Rich, T.
2011Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearingFasquelle, L.; Scott, H.; Lenoir, M.; Wang, J.; Rebillard, G.; Gaboyard, S.; Venteo, S.; Francois, F.; Masset-Bonnefont, A.; Antonarakis, S.; Neidhart, E.; Chabbert, C.; Puel, J.; Guipponi, M.; Delprat, B.
2010Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndromeJongmans, M.; Kuiper, R.; Carmichael, C.; Wilkins, E.; Dors, N.; Carmagnac, A.; Schouten-van Meeteren, N.; Li, X.; Stankovic, M.; Kamping, E.; Bengtsson, H.; Schoenmakers, M.; Geurts van Kessel, A.; Hoogerbrugge, P.; Hahn, C.; Brons, P.; Scott, H.; Hoogerbrugge, N.
2013A comparative analysis of algorithms for somatic SNV detection in cancerRoberts, N.; Kortschak, R.; Parker, W.; Schreiber, A.; Branford, S.; Scott, H.; Glonek, G.; Adelson, D.
1997Molecular defects in Sanfilippo syndrome type ABlanch, L.; Weber, B.; Guo, X.H.; Scott, H.; Hopwood, J.
2012Spliceosome mutations in hematopoietic malignanciesHahn, C.; Scott, H.
2008Two novel JAK2 exon 12 mutations in JAK2V617F-negative polycythaemia vera patientsButcher, C.; Hahn, U.; To, L.; Gecz, J.; Wilkins, E.; Scott, H.; Bardy, P.; D'Andrea, R.
2011Sensitive detection of BCR-ABL1 mutations in patients with chronic myeloid leukemia after Imatinib resistance is predictive of outcome during subsequent therapyParker, W.; Lawrence, R.; Ho, M.; Irwin, D.; Scott, H.; Hughes, T.; Branford, S.
2012Poor response to second-line kinase inhibitors in chronic myeloid leukemia patients with multiple low-level mutations, irrespective of their resistance profileParker, W.; Ho, M.; Scott, H.; Hughes, T.; Branford, S.
2011Investigating the potential role of genetic and epigenetic variation of DNA methyltransferase genes in hyperplastic polyposis syndromeDrini, M.; Wong, N.; Scott, H.; Craig, J.; Dobrovic, A.; Hewitt, C.; Dow, C.; Young, J.; Jenkins, M.; Saffery, R.; Macrae, F.; Oshima, R.

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