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Results: 1-25 | 26-36
Results: 1-25/36
Molecular and clinical characteristics of MSH6 variants: An analysis of 25index carriers of a germline variant
Authors: Berends, MJW Wu, Y Sijmons, RH Mensink, RGJ van der Sluis, T Hordijk-Hos, JM de Vries, EGE Hollema, H Karrenbeld, A Buys, CHCM van der Zee, AGJ Hofstra, RMW Kleibeuker, JH
Citation: Mjw. Berends et al., Molecular and clinical characteristics of MSH6 variants: An analysis of 25index carriers of a germline variant, AM J HU GEN, 70(1), 2002, pp. 26-37
Persistent failures in gene repair
Authors: van der Steege, G Schuilenga-Hut, PHL Buys, CHCM Scheffer, H Pas, HH Jonkman, MF
Citation: G. Van Der Steege et al., Persistent failures in gene repair, NAT BIOTECH, 19(4), 2001, pp. 305-306
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
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
Allelic gains and losses in distinct regions of chromosome 6 in gastric carcinoma
Authors: Carvalho, B van der Veen, AY Gartner, F Carneiro, F Seruca, R Buys, CHCM Kok, K
Citation: B. Carvalho et al., Allelic gains and losses in distinct regions of chromosome 6 in gastric carcinoma, CANC GENET, 131(1), 2001, pp. 54-59
Clinical definition of hereditary non-polyposis colorectal cancer: A search for the impossible?
Authors: Berends, MJW Wu, Y Sijmons, RH Hofstra, RMW van der Zee, AGJ Buys, CHCM Kleibeuker, JH
Citation: Mjw. Berends et al., Clinical definition of hereditary non-polyposis colorectal cancer: A search for the impossible?, SC J GASTR, 36, 2001, pp. 61-67
MLH1 and MSH2 protein expression as a pre-screening marker in hereditary and non-hereditary endometrial hyperplasia and cancer
Authors: Berends, MJW Hollema, H Wu, Y van der Sluis, T Mensink, RGJ ten Hoor, KA Sijmons, RH de Vries, EGE Pras, E Mourits, MJE Hofstra, RMW Buys, CHCM Kleibeuker, JH van der Zee, AGJ
Citation: Mjw. Berends et al., MLH1 and MSH2 protein expression as a pre-screening marker in hereditary and non-hereditary endometrial hyperplasia and cancer, INT J CANC, 92(3), 2001, pp. 398-403
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
The epithelial glycoprotein 2 (EGP-2) promoter-driven epithelial-specific expression of EGP-2 in transgenic mice: A new model to study carcinoma-directed immunotherapy
Authors: McLaughlin, PMJ Harmsen, MC Dokter, WHA Kroesen, BJ van der Molen, H Brinker, MGL Hollema, H Ruiters, MHJ Buys, CHCM de Leij, LFMH
Citation: Pmj. Mclaughlin et al., The epithelial glycoprotein 2 (EGP-2) promoter-driven epithelial-specific expression of EGP-2 in transgenic mice: A new model to study carcinoma-directed immunotherapy, CANCER RES, 61(10), 2001, pp. 4105-4111
RET and GDNF gene scanning in Hirschprung patients using two dual denaturing gel systems
Authors: Hofstra, RMW Wu, Y Stulp, RP Elfferich, P Osinga, J Maas, SM Siderius, L Brooks, AS Von der Ende, JJ Heydendael, VMR Severijnen, RSVM Bax, KMA Meijers, C Buys, CHCM
Citation: Rmw. Hofstra et al., RET and GDNF gene scanning in Hirschprung patients using two dual denaturing gel systems, HUM MUTAT, 15(5), 2000, pp. 418-429
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
Somatic mutations of the APC, KRAS, and TP53 genes in nonpolypoid colorectal adenomas
Authors: van Wyk, R Slezak, P Hayes, VM Buys, CHCM Kotze, MJ de Jong, G Rubio, C Dolk, A Jaramillo, E Koizumi, K Grobbelaar, JJ
Citation: R. Van Wyk et al., Somatic mutations of the APC, KRAS, and TP53 genes in nonpolypoid colorectal adenomas, GENE CHROM, 27(2), 2000, pp. 202-208
SMA carrier testing - validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletion
Authors: Scheffer, H Cobben, JM Mensink, RGJ Stulp, RP van der Steege, G Buys, CHCM
Citation: H. Scheffer et al., SMA carrier testing - validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletion, EUR J HUM G, 8(2), 2000, pp. 79-86
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
Inclusion of new microsatellite repeats in allelic loss analysis excludes retention of heterozygosity in the renal cell carcinoma critical region in 3p21
Authors: Kok, K Draaijers, TG Mosselaar, A de Long, D Buys, CHCM
Citation: K. Kok et al., Inclusion of new microsatellite repeats in allelic loss analysis excludes retention of heterozygosity in the renal cell carcinoma critical region in 3p21, CANC GENET, 116(1), 2000, pp. 40-43
Telomeres, telomerase, and cancer.
Authors: Buys, CHCM
Citation: Chcm. Buys, Telomeres, telomerase, and cancer., N ENG J MED, 342(17), 2000, pp. 1282-1283
A human model for multigenic inheritance: Phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus
Authors: Bolk, S Pelet, A Hofstra, RMW Angrist, M Salomon, R Croaker, D Buys, CHCM Lyonnet, S Chakravarti, A
Citation: S. Bolk et al., A human model for multigenic inheritance: Phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus, P NAS US, 97(1), 2000, pp. 268-273
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
The ubiquitin-activating enzyme E1-like protein in lung cancer cell lines
Authors: McLaughlin, PMJ Helfrich, W Kok, K Mulder, M Hu, SW Brinker, MGL Ruiters, MHJ de Leij, LFMH Buys, CHCM
Citation: Pmj. Mclaughlin et al., The ubiquitin-activating enzyme E1-like protein in lung cancer cell lines, INT J CANC, 85(6), 2000, pp. 871-876
Reduced endothelin-3 expression in sporadic Hirschsprung disease
Authors: Kenny, SE Hofstra, RMW Buys, CHCM Vaillant, CR Lloyd, DA Edgar, DH
Citation: Se. Kenny et al., Reduced endothelin-3 expression in sporadic Hirschsprung disease, BR J SURG, 87(5), 2000, pp. 580-585
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
Substantial reduction of the gastric carcinoma critical region at 6q16.3-q23.1
Authors: Carvalho, B Seruca, R Carneiro, F Buys, CHCM Kok, K
Citation: B. Carvalho et al., Substantial reduction of the gastric carcinoma critical region at 6q16.3-q23.1, GENE CHROM, 26(1), 1999, pp. 29-34
A comparison of genomic structures and expression patterns of two closely related flanking genes in a critical lung cancer region at 3p21.3
Authors: Timmer, T Terpstra, P van den Berg, A Veldhuis, PMJF Ter Elst, A Voutsinas, G Hulsbeek, MMF Draaijers, TG Looman, MWG Kok, K Naylor, SL Buys, CHCM
Citation: T. Timmer et al., A comparison of genomic structures and expression patterns of two closely related flanking genes in a critical lung cancer region at 3p21.3, EUR J HUM G, 7(4), 1999, pp. 478-486
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
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