Eccles M
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Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
O Ogawa, MR Eccles, J Szeto, LA McNoe, K Yun, MA Maw, PJ Smith, ...
Nature 362 (6422), 749-751, 1993
Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux
P Sanyanusin, LA Schimmenti, LA McNoe, TA Ward, MEM Pierpont, ...
Nature genetics 9 (4), 358-364, 1995
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2
EW Jabs, X Li, AF Scott, G Meyers, W Chen, M Eccles, J Mao, LR Charnas, ...
Nature genetics 8 (3), 275-279, 1994
Conjugate for efficient delivery of short interfering RNA (siRNA) into mammalian cells
A Muratovska, MR Eccles
FEBS letters 558 (1-3), 63-68, 2004
Expression of insulin-like growth factor-II transcripts in Wilms' tumour
AE Reeve, MR Eccles, RJ Wilkins, GI Bell, LJ Millow
Nature 317 (6034), 258-260, 1985
A PANorama of PAX genes in cancer and development
EJD Robson, SJ He, MR Eccles
Nature Reviews Cancer 6 (1), 52-62, 2006
Paired-Box genes are frequently expressed in cancer and often required for cancer cell survival
A Muratovska, C Zhou, S He, P Goodyer, MR Eccles
Oncogene 22 (39), 7989-7997, 2003
Epigenetic drivers of tumourigenesis and cancer metastasis
A Chatterjee, EJ Rodger, MR Eccles
Seminars in cancer biology 51, 149-159, 2018
Application of circularly polarized light for non‐invasive diagnosis of cancerous tissues and turbid tissue‐like scattering media
B Kunnen, C Macdonald, A Doronin, S Jacques, M Eccles, I Meglinski
Journal of biophotonics 8 (4), 317-323, 2015
A third Wilms' tumor locus on chromosome 16q
MA Maw, PE Grundy, LJ Millow, MR Eccles, RS Dunn, PJ Smith, ...
Cancer research 52 (11), 3094-3098, 1992
Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux
W Lu, AM Van Eerde, X Fan, F Quintero-Rivera, S Kulkarni, H Ferguson, ...
The American Journal of Human Genetics 80 (4), 616-632, 2007
Primary renal hypoplasiain humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax21Neu +/– mutant mice
S Porteous, E Torban, NP Cho, H Cunliffe, L Chua, L McNoe, T Ward, ...
Human molecular genetics 9 (1), 1-11, 2000
Mutation of PAX2 in two siblings with renal-coloboma syndrome
P Sanyanusin, LA McNoe, MJ Sullivan, RG Weaver, MR Eccles
Human molecular genetics 4 (11), 2183-2184, 1995
Targeting DNA methylation and EZH2 activity to overcome melanoma resistance to immunotherapy
A Al Emran, A Chatterjee, EJ Rodger, JC Tiffen, SJ Gallagher, MR Eccles, ...
Trends in immunology 40 (4), 328-344, 2019
Expression of the PAX2 gene in human fetal kidney and Wilms' tumor
MR Eccles, LJ Wallis, AE Fidler, NK Spurr, PJ Goodfellow, AE Reeve
Cell Growth Differ 3 (5), 279-289, 1992
Renal‐coloboma syndrome: a multi‐system developmental disorder caused by PAX2 mutations
MR Eccles, LA Schimmenti
Clinical genetics 56 (1), 1-9, 1999
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy
HF Otto EA, Ramaswami G, Janssen S, Chaki M, Allen SJ, Zhou W, Airik R, Hurd ...
J Med. Genet. 48 (2), 105-116, 2011
Promoter DNA hypermethylation and paradoxical gene activation
J Smith, S Sen, RJ Weeks, MR Eccles, A Chatterjee
Trends in cancer 6 (5), 392-406, 2020
Biallelic DICER1 mutations occur in Wilms tumours
MK Wu, N Sabbaghian, B Xu, S Addidou‐Kalucki, C Bernard, D Zou, ...
The Journal of pathology 230 (2), 154-164, 2013
Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations.
LA Schimmenti, HE Cunliffe, LA McNoe, TA Ward, MC French, HH Shim, ...
American journal of human genetics 60 (4), 869, 1997
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