David Vetrie
David Vetrie
University of Glasgow, Institute of Cancer Sciences
Verified email at - Homepage
Cited by
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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
Management Group Liefer Laura A. 51 Wetterstrand Kris A. 51 Good Peter J. 51 ...
nature 447 (7146), 799-816, 2007
Requirement of bic/microRNA-155 for normal immune function
A Rodriguez, E Vigorito, S Clare, MV Warren, P Couttet, DR Soond, ...
Science 316 (5824), 608-611, 2007
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases
D Vetrie, I Vořechovský, P Sideras, J Holland, A Davies, F Flinter, ...
Nature 361 (6409), 226-233, 1993
DNA microarrays for comparative genomic hybridization based on DOP‐PCR amplification of BAC and PAC clones
H Fiegler, P Carr, EJ Douglas, DC Burford, S Hunt, J Smith, D Vetrie, ...
Genes, Chromosomes and Cancer 36 (4), 361-374, 2003
The landscape of histone modifications across 1% of the human genome in five human cell lines
CM Koch, RM Andrews, P Flicek, SC Dillon, U Karaöz, GK Clelland, ...
Genome research 17 (6), 691-707, 2007
A novel X–linked gene, DDP, shows mutations in families with deafness (DFN–1), dystonia, mental deficiency and blindness
H Jin, M May, L Tranebjærg, E Kendall, G Fontán, J Jackson, ...
Nature genetics 14 (2), 177-180, 1996
The chronic myeloid leukemia stem cell: stemming the tide of persistence
TL Holyoake, D Vetrie
Blood, The Journal of the American Society of Hematology 129 (12), 1595-1606, 2017
Whole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array data
R Lyne, G Burns, J Mata, CJ Penkett, G Rustici, D Chen, C Langford, ...
BMC genomics 4 (1), 1-15, 2003
Baylor College of Medicine Human Genome Sequencing Center; Washington University Genome Sequencing Center; Broad Institute; Children’s Hospital Oakland Research Institute.(2007 …
E Birney, JA Stamatoyannopoulos, A Dutta, R Guigó, TR Gingeras, ...
Nature 447 (7146), 799-816, 2007
Dual targeting of p53 and c-MYC selectively eliminates leukaemic stem cells
SA Abraham, LEM Hopcroft, E Carrick, ME Drotar, K Dunn, ...
Nature 534 (7607), 341-346, 2016
Structural instability of human tandemly repeated DNA sequences cloned in yeast artificial chromosome vectors
DL Neil, A Villasante, RB Fisher, D Vetrie, B Cox, C Tyler-Smit
Nucleic Acids Research 18 (6), 1421-1428, 1990
Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome
P Dhami, AJ Coffey, S Abbs, JR Vermeesch, JP Dumanski, KJ Woodward, ...
The American Journal of Human Genetics 76 (5), 750-762, 2005
Pelizaeus-Merzbacher disease: identification of Xq22 proteolipid-protein duplications and characterization of breakpoints by interphase FISH
K Woodward, E Kendall, D Vetrie, S Malcolm
The American Journal of Human Genetics 63 (1), 207-217, 1998
The leukaemia stem cell: similarities, differences and clinical prospects in CML and AML
D Vetrie, GV Helgason, M Copland
Nature Reviews Cancer 20 (3), 158-173, 2020
Expression profiling of the Leishmania life cycle: cDNA arrays identify developmentally regulated genes present but not annotated in the genome
R Almeida, BJ Gilmartin, SH McCann, A Norrish, AC Ivens, D Lawson, ...
Molecular and Biochemical Parasitology 136 (1), 87-100, 2004
Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technology
A Pellagatti, N Esoof, F Watkins, CF Langford, D Vetrie, LJ Campbell, ...
British journal of haematology 125 (5), 576-583, 2004
Epigenetic Reprogramming Sensitizes CML Stem Cells to Combined EZH2 and Tyrosine Kinase InhibitionEZH2 and Tyrosine Kinase Inhibition in CML Stem Cells
MT Scott, K Korfi, P Saffrey, LEM Hopcroft, R Kinstrie, F Pellicano, ...
Cancer discovery 6 (11), 1248-1257, 2016
Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays
A Rada-Iglesias, O Wallerman, C Koch, A Ameur, S Enroth, G Clelland, ...
Human molecular genetics 14 (22), 3435-3447, 2005
Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease.
M Vihinen, D Vetrie, HS Maniar, HD Ochs, Q Zhu, I Vorechovský, ...
Proceedings of the National Academy of Sciences 91 (26), 12803-12807, 1994
Functional diversity for REST (NRSF) is defined by in vivo binding affinity hierarchies at the DNA sequence level
AW Bruce, AJ López-Contreras, P Flicek, TA Down, P Dhami, SC Dillon, ...
Genome research 19 (6), 994-1005, 2009
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