|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, 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, 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, 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, 1985
|A PANorama of PAX genes in cancer and development|
EJD Robson, SJ He, MR Eccles
Nature Reviews Cancer 6 (1), 52, 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, 2003
|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
|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
|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
|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
|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
|Renal‐coloboma syndrome: a multi‐system developmental disorder caused by PAX2 mutations|
MR Eccles, LA Schimmenti
Clinical genetics 56 (1), 1-9, 1999
|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
|Constitutional relaxation of insulin–like growth factor II gene imprinting associated with Wilms' tumour and gigantism|
O Ogawa, DM Becroft, IM Morison, MR Eccles, JE Skeen, DC Mauger, ...
Nature genetics 5 (4), 408, 1993
|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
|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
|PAX genes in development and disease: the role of PAX2 in urogenital tract development.|
MR Eccles, S He, M Legge, R Kumar, J Fox, C Zhou, M French, RWS Tsai
International Journal of Developmental Biology 46 (4), 535-544, 2004
|PAX2 suppresses apoptosis in renal collecting duct cells|
E Torban, MR Eccles, J Favor, PR Goodyer
The American journal of pathology 157 (3), 833-842, 2000
|Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome|
B Utsch, JA Sayer, M Attanasio, RR Pereira, M Eccles, HC Hennies, ...
Pediatric nephrology 21 (1), 32-35, 2006