Andrew Perkins
Andrew Perkins
Professor of Cancer Genomics
Verified email at - Homepage
Cited by
Cited by
Stem cell transcriptome profiling via massive-scale mRNA sequencing
N Cloonan, ARR Forrest, G Kolle, BBA Gardiner, GJ Faulkner, MK Brown, ...
Nature methods 5 (7), 613-619, 2008
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation
ME Dinger, PP Amaral, TR Mercer, KC Pang, SJ Bruce, BB Gardiner, ...
Genome research 18 (9), 1433-1445, 2008
Lethal β-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF
AC Parkins, AH Sharpe, SH Orkin
Nature 375 (6529), 318-322, 1995
An essential role in liver development for transcription factor XBP-1
AM Reimold, A Etkin, I Clauss, A Perkins, DS Friend, J Zhang, HF Horton, ...
Genes & development 14 (2), 152-157, 2000
High fat diets induce colonic epithelial cell stress and inflammation that is reversed by IL-22
M Gulhane, L Murray, R Lourie, H Tong, YH Sheng, R Wang, A Kang, ...
Scientific reports 6 (1), 28990, 2016
Isolation and characterization of the cDNA encoding BKLF/TEF-2, a major CACCC-box-binding protein in erythroid cells and selected other cells
M Crossley, E Whitelaw, A Perkins, G Williams, Y Fujiwara, SH Orkin
Molecular and cellular biology, 1996
Pacritinib versus best available therapy for the treatment of myelofibrosis irrespective of baseline cytopenias (PERSIST-1): an international, randomised, phase 3 trial
RA Mesa, AM Vannucchi, A Mead, M Egyed, A Szoke, A Suvorov, ...
The Lancet Haematology 4 (5), e225-e236, 2017
A global role for EKLF in definitive and primitive erythropoiesis
D Hodge, E Coghill, J Keys, T Maguire, B Hartmann, A McDowall, ...
Blood 107 (8), 3359-3370, 2006
SEK1 deficiency reveals mitogen-activated protein kinase cascade crossregulation and leads to abnormal hepatogenesis
S Ganiatsas, L Kwee, Y Fujiwara, A Perkins, T Ikeda, MA Labow, LI Zon
Proceedings of the National Academy of Sciences 95 (12), 6881-6886, 1998
A pooled analysis of overall survival in COMFORT-I and COMFORT-II, 2 randomized phase III trials of ruxolitinib for the treatment of myelofibrosis
AM Vannucchi, HM Kantarjian, JJ Kiladjian, J Gotlib, F Cervantes, ...
haematologica 100 (9), 1139, 2015
Efficacy, safety, and survival with ruxolitinib in patients with myelofibrosis: results of a median 3-year follow-up of COMFORT-I
S Verstovsek, RA Mesa, J Gotlib, RS Levy, V Gupta, JF DiPersio, ...
haematologica 100 (4), 479, 2015
A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells
MR Tallack, T Whitington, WS Yuen, EN Wainwright, JR Keys, ...
Genome research 20 (8), 1052-1063, 2010
Complex architecture and regulated expression of the Sox2ot locus during vertebrate development
PP Amaral, C Neyt, SJ Wilkins, ME Askarian-Amiri, SM Sunkin, ...
Rna 15 (11), 2013-2027, 2009
Evolution of gene function and regulatory control after whole-genome duplication: comparative analyses in vertebrates
KS Kassahn, VT Dang, SJ Wilkins, AC Perkins, MA Ragan
Genome research 19 (8), 1404-1418, 2009
Thrombopoietin rescues in vitro erythroid colony formation from mouse embryos lacking the erythropoietin receptor.
MW Kieran, AC Perkins, SH Orkin, LI Zon
Proceedings of the National Academy of Sciences 93 (17), 9126-9131, 1996
Targeted Disruption of the Basic Krüppel-Like Factor Gene (Klf3) Reveals a Role in Adipogenesis
N Sue, BHA Jack, SA Eaton, RCM Pearson, APW Funnell, J Turner, ...
Molecular and cellular biology 28 (12), 3967-3978, 2008
Homeobox gene expression plus autocrine growth factor production elicits myeloid leukemia.
A Perkins, K Kongsuwan, J Visvader, JM Adams, S Cory
Proceedings of the National Academy of Sciences 87 (21), 8398-8402, 1990
Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease
H Lu, MCR Galeano, E Ott, G Kaeslin, PJ Kausalya, C Kramer, ...
Nature genetics 49 (7), 1025-1034, 2017
Silencing of human fetal globin expression is impaired in the absence of the adult beta-globin gene activator protein EKLF.
AC Perkins, KM Gaensler, SH Orkin
Proceedings of the National Academy of Sciences 93 (22), 12267-12271, 1996
Widespread failure of hematolymphoid differentiation caused by a recessive niche-filling allele of the Ikaros transcription factor
P Papathanasiou, AC Perkins, BS Cobb, R Ferrini, R Sridharan, ...
Immunity 19 (1), 131-144, 2003
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