Slow proliferation as a biological feature of colorectal cancer metastasis
Anjomshoaa, A, Nasri, S, Humar, B, McCall, J L, Chatterjee, A, Yoon, H-S, McNoe, L, Black, M A, Reeve, A E
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Published in British journal of cancer (01.09.2009)
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Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes
Fukuzawa, R, Anaka, MR, Heathcott, RW, McNoe, LA, Morison, IM, Perlman, EJ, Reeve, AE
Published in The Journal of pathology (01.08.2008)
Published in The Journal of pathology (01.08.2008)
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Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux
Sanyanusin, Phaikasame, Schimmenti, Lisa A, McNoe, Leslie A, Ward, Teresa A, Pierpont, Mary Ella M, Sullivan, Michael J, Dobyns, William B, Eccles, Michael R
Published in Nature genetics (01.04.1995)
Published in Nature genetics (01.04.1995)
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Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
Ogawa, Osamu, Eccles, Michael R, Szeto, Jenny, McNoe, Leslie A, Yun, Kankatsu, Maw, Marion A, Smith, Peter J, Reeve, Anthony E
Published in Nature (London) (22.04.1993)
Published in Nature (London) (22.04.1993)
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Mutation of PAX2 in two siblings with renal-coloboma syndrome
Sanyanusin, P, McNoe, L A, Sullivan, M J, Weaver, R G, Eccles, M R
Published in Human molecular genetics (01.11.1995)
Published in Human molecular genetics (01.11.1995)
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Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations
SCHIMMENTI, L. A, CUNLIFFE, H. E, BRADDOCK, S. R, MASUNO, M, IMAIZUMI, K, DEVRIENDT, K, ECCLES, M. R, MCNOE, L. A, WARD, T. A, FRENCH, M. C, SHIM, H. H, ZHANG, Y.-H, PROESMANS, W, LEYS, A, BYERLY, K. A
Published in American journal of human genetics (01.04.1997)
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Published in American journal of human genetics (01.04.1997)
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Human insulin-like growth factor type I and type II receptors are not imprinted
Ogawa, O, McNoe, L A, Eccles, M R, Morison, I M, Reeve, A E
Published in Human molecular genetics (01.12.1993)
Published in Human molecular genetics (01.12.1993)
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Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux
Choi, K L, McNoe, L A, French, M C, Guilford, P J, Eccles, M R
Published in Journal of medical genetics (01.04.1998)
Published in Journal of medical genetics (01.04.1998)
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Genomic structure of the human PAX2 gene
SANYANUSIN, P, NORRISH, J. H, WARD, T. A, NEBEL, A, MCNOE, L. A, ECCLES, M. R
Published in Genomics (San Diego, Calif.) (01.07.1996)
Published in Genomics (San Diego, Calif.) (01.07.1996)
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The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissues
Pilbrow, Anna P, Folkersen, Lasse, Pearson, John F, Brown, Chris M, McNoe, Les, Wang, Nancy M, Sweet, Wendy E, Tang, W H Wilson, Black, Michael A, Troughton, Richard W, Richards, A Mark, Franco-Cereceda, Anders, Gabrielsen, Anders, Eriksson, Per, Moravec, Christine S, Cameron, Vicky A
Published in PloS one (29.06.2012)
Published in PloS one (29.06.2012)
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Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice
Porteous, S, Torban, E, Cho, N P, Cunliffe, H, Chua, L, McNoe, L, Ward, T, Souza, C, Gus, P, Giugliani, R, Sato, T, Yun, K, Favor, J, Sicotte, M, Goodyer, P, Eccles, M
Published in Human molecular genetics (01.01.2000)
Published in Human molecular genetics (01.01.2000)
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Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2 super(1Neu) +/- mutant mice
Porteous, S, Torban, E, Cho, Nam-Pyo, Cunliffe, H, Chua, Lin, McNoe, L, Ward, T, Souza, C, Gus, P, Giugliani, R, Sato, Tadashi, Yun, Kankatsu, Favor, J, Eccles, M
Published in Human molecular genetics (01.01.2000)
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Published in Human molecular genetics (01.01.2000)
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Familial fibronectin glomerulopathy: analysis of chromosome 1q32 and uteroglobin gene loci in a large New Zealand family
Walker, Robert, Dixon, Stephen, Ruger, Beate, Davis, Paul, Hildebrant, Friedhelm, Kremer, Mathias, Eccles, Michael, Mcnoe, Leslie, Watson, Michael, Reid, James
Published in Nephrology (Carlton, Vic.) (01.10.2001)
Published in Nephrology (Carlton, Vic.) (01.10.2001)
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Primary renal hypoplasia in humans and mice with PAX2 mutations : evidence of increased apoptosis in fetal kidneys of Pax21Neu +/-mutant mice
PORTEOUS, S, TORBAN, E, SATO, T, YUN, K, FAVOR, J, SICOTTE, M, GOODYER, P, ECCLES, M, CHO, N.-P, CUNLIFFE, H, LIN CHUA, MCNOE, L, WARD, T, SOUZA, C, GUS, P, GIUGLIANI, R
Published in Human molecular genetics (2000)
Published in Human molecular genetics (2000)
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Aortic dissection, patent ductus arteriosus, iris hypoplasia and brachytelephalangy in a male adolescent
Adès, L C, Davies, R, Haan, E A, Holman, K J, Watson, K C, Sreetharan, D, Cao, S N, Milewicz, D M, Bateman, J F, Chiodo, A A, Eccles, M, McNoe, L, Harbord, M
Published in Clinical dysmorphology (01.10.1999)
Published in Clinical dysmorphology (01.10.1999)
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Mutation of the gene in a family with optic nerve colobomas, renal anomolies and vesicoureteral reflux
Sanyanusin, P, Schimmenti, L A, McNoe, T A, Ward, T A, Pierpont, M E, Sullivan, M J, Dobyns, W B, Eccles, M R
Published in Nature genetics (01.05.1996)
Published in Nature genetics (01.05.1996)
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