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Results: 1-8 |
Results: 8
MEN2A-RET-induced cellular transformation by activation of STAT3
Authors: Schuringa, JJ Wojtachnio, K Hagens, W Vellenga, E Buys, CHCM Hofstra, R Kruijer, W
Citation: Jj. Schuringa et al., MEN2A-RET-induced cellular transformation by activation of STAT3, ONCOGENE, 20(38), 2001, pp. 5350-5358
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutchpedigree
Authors: Wagner, A Hendriks, Y Meijers-Heijboer, EJ de Leeuw, WJF Morreau, H Hofstra, R Tops, C Bik, E Brocker-Vriends, AHJT van der Meer, C Lindhout, D Vasen, HFA Breuning, MH Cornelisse, CJ van Krimpen, C Niermeijer, MF Zwinderman, AH Wijnen, J Fodde, R
Citation: A. Wagner et al., Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutchpedigree, J MED GENET, 38(5), 2001, pp. 318-322
Inclusion of malignant fibrous histiocytoma in the tumour spectrum associated with hereditary non-polyposis colorectal cancer
Authors: Sijmons, R Hofstra, R Hollema, H Mensink, R van der Hout, A Hoekstra, H Kleibeuker, J Molenaar, W Wijnen, J Fodde, R Vasen, H Buys, C
Citation: R. Sijmons et al., Inclusion of malignant fibrous histiocytoma in the tumour spectrum associated with hereditary non-polyposis colorectal cancer, GENE CHROM, 29(4), 2000, pp. 353-355
A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease
Authors: Griseri, P Sancandi, M Patrone, G Bocciardi, R Hofstra, R Ravazzolo, R Devoto, M Romeo, G Ceccherini, I
Citation: P. Griseri et al., A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease, EUR J HUM G, 8(9), 2000, pp. 721-724
MSI-L gastric carcinomas share the hMLH1 methylation status of MSI-H carcinomas but not their clinicopathological profile
Authors: Pinto, M Oliveira, C Machado, JC Cirnes, L Tavares, J Carneiro, F Hamelin, R Hofstra, R Seruca, R Sobrinho-Simoes, M
Citation: M. Pinto et al., MSI-L gastric carcinomas share the hMLH1 methylation status of MSI-H carcinomas but not their clinicopathological profile, LAB INV, 80(12), 2000, pp. 1915-1923
Incidence of RET mutations in patients with Hirschsprung's disease
Authors: Sancandi, M Ceccherini, I Costa, M Fava, M Chen, B Wu, Y Hofstra, R Laurie, T Griffths, M Burge, D Tam, PKH
Citation: M. Sancandi et al., Incidence of RET mutations in patients with Hirschsprung's disease, J PED SURG, 35(1), 2000, pp. 139-142
Familial endometrial cancer in female carriers of MSH6 germline mutations
Authors: Meijers-Heijboer, H Lindhout, D Menko, F Vossen, S Moslein, G Tops, C Brocker-Vriends, A Wu, Y Hofstra, R Sijmons, R Cornelisse, C Morreau, H Fodde, R
Citation: H. Meijers-heijboer et al., Familial endometrial cancer in female carriers of MSH6 germline mutations, NAT GENET, 23(2), 1999, pp. 142-144
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/ velocardiofacial syndrome without deletions within chromosome 22q11
Authors: Wadey, R McKie, J Papapetrou, C Sutherland, H Lohman, F Osinga, J Frohn, I Hofstra, R Meijers, C Amati, F Conti, E Pizzuti, A Dallapiccola, B Novelli, G Scambler, P
Citation: R. Wadey et al., Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/ velocardiofacial syndrome without deletions within chromosome 22q11, AM J HU GEN, 65(1), 1999, pp. 247-249
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