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Results: 1-9 |
Results: 9
A role for MLH3 in hereditary nonpolyposis colorectal cancer
Authors: Wu, Y Berends, MJW Sijmons, RH Mensink, RGJ Verlind, E Kooi, KA van der Sluis, T Kempinga, C van der Zee, AGJ Hollema, H Buys, CHCM Kleibeuker, JH Hofstra, RMW
Citation: Y. Wu et al., A role for MLH3 in hereditary nonpolyposis colorectal cancer, NAT GENET, 29(2), 2001, pp. 137-138
Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms
Authors: Wu, Y Berends, MJW Post, JG Mensink, RGJ Verlind, E Van Der Sluis, T Kempinga, C Sijmons, RH Van der Zee, AGJ Hollema, H Kleibeuker, JH Buys, CHCM Hofstra, RMW
Citation: Y. Wu et al., Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms, GASTROENTY, 120(7), 2001, pp. 1580-1587
Prognostic significance of K-ras and TP53 mutations in the role of adjuvant chemotherapy on survival in patients with Dukes C colon cancer
Authors: Bleeker, WA Hayes, VM Karrenbeld, A Hofstra, RMW Verlind, E Hermans, J Poppema, S Buys, CHCM Plukker, JTM
Citation: Wa. Bleeker et al., Prognostic significance of K-ras and TP53 mutations in the role of adjuvant chemotherapy on survival in patients with Dukes C colon cancer, DIS COL REC, 44(3), 2001, pp. 358-363
New comprehensive denaturing-gradient-gel-electrophoresis assay for KRAS mutation detection applied to paraffin-embedded tumours
Authors: Hayes, VM Westra, JL Verlind, E Bleeker, W Plukker, JT Hofstra, RMW Buys, CHCM
Citation: Vm. Hayes et al., New comprehensive denaturing-gradient-gel-electrophoresis assay for KRAS mutation detection applied to paraffin-embedded tumours, GENE CHROM, 29(4), 2000, pp. 309-314
Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus
Authors: Sztriha, L Frossard, P Hofstra, RMW Verlind, E Nork, M
Citation: L. Sztriha et al., Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus, J CHILD NEU, 15(4), 2000, pp. 239-243
Glycogen storage disease type Ia: recent experience with mutation analysis, a summary of mutations reported in the literature and a newly developed diagnostic flowchart
Authors: Rake, JP ten Berge, AM Visser, G Verlind, E Niezen-Koning, KE Buys, CHCM Smit, GPA Scheffer, H
Citation: Jp. Rake et al., Glycogen storage disease type Ia: recent experience with mutation analysis, a summary of mutations reported in the literature and a newly developed diagnostic flowchart, EUR J PED, 159(5), 2000, pp. 322-330
Exempting homologous pseudogene sequences from polymerase chain reaction amplification allows genomic keratin 14 hotspot mutation analysis
Authors: Hut, PHL van der Vlies, P Jonkman, MF Verlind, E Shimizu, H Buys, CHCM Scheffer, H
Citation: Phl. Hut et al., Exempting homologous pseudogene sequences from polymerase chain reaction amplification allows genomic keratin 14 hotspot mutation analysis, J INVES DER, 114(4), 2000, pp. 616-619
Comprehensive TP53-denaturing gradient gel electrophoresis mutation detection assay also applicable to archival paraffin-embedded tissue
Authors: Hayes, VM Bleeker, W Verlind, E Timmer, T Karrenbeld, A Plukker, JT Marx, MP Hofstra, RMW Buys, CHCM
Citation: Vm. Hayes et al., Comprehensive TP53-denaturing gradient gel electrophoresis mutation detection assay also applicable to archival paraffin-embedded tissue, DIAGN MOL P, 8(1), 1999, pp. 2-10
High frequency of TP53 mutations in juvenile pilocytic astrocytomas indicates role of TP53 in the development of these tumors
Authors: Hayes, VM Dirven, CMF Dam, A Verlind, E Molenaar, WM Mooij, JJA Hofstra, RMW Buys, CHCM
Citation: Vm. Hayes et al., High frequency of TP53 mutations in juvenile pilocytic astrocytomas indicates role of TP53 in the development of these tumors, BRAIN PATH, 9(3), 1999, pp. 463-467
Risultati: 1-9 |