Slow proliferation as a biological feature of colorectal cancer metastasis von 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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Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes von Fukuzawa, R, Anaka, MR, Heathcott, RW, McNoe, LA, Morison, IM, Perlman, EJ, Reeve, AE

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Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux von Sanyanusin, Phaikasame, Schimmenti, Lisa A, McNoe, Leslie A, Ward, Teresa A, Pierpont, Mary Ella M, Sullivan, Michael J, Dobyns, William B, Eccles, Michael R

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Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour von Ogawa, Osamu, Eccles, Michael R, Szeto, Jenny, McNoe, Leslie A, Yun, Kankatsu, Maw, Marion A, Smith, Peter J, Reeve, Anthony E

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Mutation of PAX2 in two siblings with renal-coloboma syndrome von Sanyanusin, Phaikasame, McNoe, Leslie A., Sullivan, Michael J., Weaver, R.Grey, Eccles, Michael R.

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Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations von 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

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The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomalies von Cunliffe, H E, McNoe, L A, Ward, T A, Devriendt, K, Brunner, H G, Eccles, M R

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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 von 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

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Human insulin-like growth factor type I and type II receptors are not imprinted von Ogawa, Osamu, McNoe, Leslie A., Eccles, Michael R., Morison, lan M., Reeve, Anthony E.

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Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux von Choi, K L, McNoe, L A, French, M C, Guilford, P J, Eccles, M R

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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 von 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

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Genomic structure of the human PAX2 gene von SANYANUSIN, P, NORRISH, J. H, WARD, T. A, NEBEL, A, MCNOE, L. A, ECCLES, M. R

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Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologies von Erickson, Robert P., Stone, J. F., McNoe, Leslie A., Eccles, Michael R.

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Dinucleotide repeat polymorphism at the D11S860 locus von McNoe, L.A, Eccles, M.R., Reeve, A.E.

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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 von 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

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Mutation of the gene in a family with optic nerve colobomas, renal anomolies and vesicoureteral reflux von Sanyanusin, P, Schimmenti, L A, McNoe, T A, Ward, T A, Pierpont, M E, Sullivan, M J, Dobyns, W B, Eccles, M R

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Familial fibronectin glomerulopathy: analysis of chromosome 1q32 and uteroglobin gene loci in a large New Zealand family von Walker, Robert, Dixon, Stephen, Ruger, Beate, Davis, Paul, Hildebrant, Friedhelm, Kremer, Mathias, Eccles, Michael, Mcnoe, Leslie, Watson, Michael, Reid, James

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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 von 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

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Aortic dissection, patent ductus arteriosus, iris hypoplasia and brachytelephalangy in a male adolescent von 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

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The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney von Favor, J, Sandulache, R, Neuhäuser-Klaus, A, Pretsch, W, Chatterjee, B, Senft, E, Wurst, W, Blanquet, V, Grimes, P, Spörle, R, Schughart, K

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