Search results (34)
« Back to PublicationsSilencing of SOD1 sensitises ATRX-deficient cells to camptothecin treatment through increased activity of the alternative lengthening of telomeres pathway.
Journal article
Mattis N. et al, (2025), Hum Mol Genet, 34, 1638 - 1647
Elevated reactive oxygen species can drive the alternative lengthening of telomeres pathway in ATRX-null cancers.
Journal article
Goncalves T. et al, (2025), Nucleic Acids Res, 53
Elevated reactive oxygen species can drive the alternative lengthening of telomeres pathway in ATRX-null cancers.
Journal article
Goncalves T. et al, (2025), Nucleic Acids Res, 53
Phosphorylation of 'SDT-like' motifs in ATRX mediates its interaction with the MRN complex and is important for ALT pathway suppression.
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Goncalves T. et al, (2024), Open Biol, 14
Hypoxia-induced transcriptional stress is mediated by ROS-induced R-loops.
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Ma TS. et al, (2023), Nucleic Acids Res, 51, 11584 - 11599
Induction of the alternative lengthening of telomeres pathway by trapping of proteins on DNA.
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Rose AM. et al, (2023), Nucleic Acids Res, 51, 6509 - 6527
Ethnicity, child health and paediatric services.
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Qureshi Z. et al, (2023), Arch Dis Child, 108, 453 - 454
The emergence of Fanconi anaemia type S: a phenotypic spectrum of biallelic BRCA1 mutations.
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Hughes T. and Rose AM., (2023), Front Oncol, 13
Risk and Lag-time for Development of Lacrimal Gland Carcinoma Expleomorphic Adenoma: Observations and Conjectural Study.
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Rose GE. et al, (2022), Ophthalmic Plast Reconstr Surg, 38, 563 - 566
Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.
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Scott C. et al, (2021), Haematologica, 106, 2960 - 2970
A remarkable case of HbH disease illustrates the relative contributions of the α-globin enhancers to gene expression.
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Badat M. et al, (2021), Blood, 137, 572 - 575
Anti-neutrophil cytoplasmic antibody-positive vasculitis secondary to therapeutic levamisole.
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Rose AM., (2020), Rheumatology (Oxford)
Detection of mutations in SF3B1, EIF1AX and GNAQ in primary orbital melanoma by candidate gene analysis.
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Rose AM. et al, (2018), BMC Cancer, 18
Cancer and the junkyard chromosome: how repeat DNA sequence on chromosome 19 influences risk of malignant disease.
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Rose AM., (2018), Oncotarget, 9, 31942 - 31944
Hb Penang [β78(EF2)Leu→Pro, HBB: c.236T>C]: a Novel β-Globin Variant.
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Hsu CH-W. et al, (2018), Hemoglobin, 42, 199 - 202