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Results: 1-25 |
Results: 25
Ever since Knudson
Authors: Devilee, P Cleton-Jansen, AM Cornelisse, CJ
Citation: P. Devilee et al., Ever since Knudson, TRENDS GEN, 17(10), 2001, pp. 569-573
Chondrosarcoma is not characterized by detectable telomerase activity
Authors: Bovee, JVMG van den Broek, LJCM Cleton-Jansen, AM Hogendoom, PCW
Citation: Jvmg. Bovee et al., Chondrosarcoma is not characterized by detectable telomerase activity, J PATHOLOGY, 193(3), 2001, pp. 354-360
An association between cartilaginous tumours and breast cancer in the national pathology registration in The Netherlands points towards a possible genetic trait
Authors: Odink, AE van Asperen, CJ Vandenbroucke, JP Cleton-Jansen, AM Hogendoom, PCW
Citation: Ae. Odink et al., An association between cartilaginous tumours and breast cancer in the national pathology registration in The Netherlands points towards a possible genetic trait, J PATHOLOGY, 193(2), 2001, pp. 190-192
High quality RNA isolation from tumours with low cellularity and high extracellular matrix component for cDNA microarrays: application to chondrosarcoma
Authors: Baelde, HJ Cleton-Jansen, AM van Beerendonk, H Namba, M Bovee, JVMG Hogendoorn, PCW
Citation: Hj. Baelde et al., High quality RNA isolation from tumours with low cellularity and high extracellular matrix component for cDNA microarrays: application to chondrosarcoma, J CLIN PATH, 54(10), 2001, pp. 778-782
Structural organization and regulation of the small proline-rich family ofcornified envelope precursors suggest a role in adaptive barrier function
Authors: Cabral, A Voskamp, P Cleton-Jansen, AM South, A Nizetic, D Backendorf, C
Citation: A. Cabral et al., Structural organization and regulation of the small proline-rich family ofcornified envelope precursors suggest a role in adaptive barrier function, J BIOL CHEM, 276(22), 2001, pp. 19231-19237
Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions
Authors: Cleton-Jansen, AM Callen, DF Seshadri, R Goldup, S McCallum, B Crawford, J Powell, JA Settasatian, C van Beerendonk, H Moerland, EW Smit, VTBHM Harris, WH Millis, R Morgan, NV Barnes, D Mathew, CG Cornelisse, CJ
Citation: Am. Cleton-jansen et al., Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions, CANCER RES, 61(3), 2001, pp. 1171-1177
Malignant melanoma is genetically distinct from clear cell sarcoma of tendons and aponeurosis (malignant melanoma of soft parts)
Authors: Langezaal, SM van Roggen, JFG Cleton-Jansen, AM Baelde, JJ Hogendoorn, PCW
Citation: Sm. Langezaal et al., Malignant melanoma is genetically distinct from clear cell sarcoma of tendons and aponeurosis (malignant melanoma of soft parts), BR J CANC, 84(4), 2001, pp. 535-538
Allelotype analysis of flow-sorted breast cancer cells demonstrates genetically related diploid and aneuploid subpopulations in primary tumors and lymph node metastases
Authors: Bonsing, BA Corver, WE Fleuren, GJ Cleton-Jansen, AM Devilee, P Cornelisse, CJ
Citation: Ba. Bonsing et al., Allelotype analysis of flow-sorted breast cancer cells demonstrates genetically related diploid and aneuploid subpopulations in primary tumors and lymph node metastases, GENE CHROM, 28(2), 2000, pp. 173-183
A sporadic breast tumor with a somatically acquired complex genomic rearrangement in BRCA1
Authors: van der Looij, M Cleton-Jansen, AM van Eijk, R Morreau, H van Vliet, M Kuipers-Dijkshoorn, N Olah, E Cornelisse, CJ Devilee, P
Citation: M. Van Der Looij et al., A sporadic breast tumor with a somatically acquired complex genomic rearrangement in BRCA1, GENE CHROM, 27(3), 2000, pp. 295-302
Molecular evidence of field cancerization in a patient with 7 tumors of the aerodigestive tract
Authors: van Rees, BP Cleton-Jansen, AM Cense, HA Polak, MM Clement, MJ Drillenburg, P van Lanschot, JJB Offerhaus, GJA
Citation: Bp. Van Rees et al., Molecular evidence of field cancerization in a patient with 7 tumors of the aerodigestive tract, HUMAN PATH, 31(2), 2000, pp. 269-271
PCR artifacts in LOH and MSI analysis of microdissected tumor cells
Authors: Sieben, NLG ter Haar, NT Cornelisse, CJ Fleuren, GJ Cleton-Jansen, AM
Citation: Nlg. Sieben et al., PCR artifacts in LOH and MSI analysis of microdissected tumor cells, HUMAN PATH, 31(11), 2000, pp. 1414-1419
Malignant progression in multiple enchondromatosis (Ollier's disease): An autopsy-based molecular genetic study
Authors: Bovee, JVMG van Roggen, JFG Cleton-Jansen, AM Taminiau, AHM van der Woude, HJ Hogendoorn, PCW
Citation: Jvmg. Bovee et al., Malignant progression in multiple enchondromatosis (Ollier's disease): An autopsy-based molecular genetic study, HUMAN PATH, 31(10), 2000, pp. 1299-1303
Up-regulation of PTHrP and Bcl-2 expression characterizes the progression of osteochondroma towards peripheral chondrosarcoma and is a late event in central chondrosarcoma
Authors: Bovee, JVMG van den Broek, LJCM Cleton-Jansen, AM Hogendoorn, PCW
Citation: Jvmg. Bovee et al., Up-regulation of PTHrP and Bcl-2 expression characterizes the progression of osteochondroma towards peripheral chondrosarcoma and is a late event in central chondrosarcoma, LAB INV, 80(12), 2000, pp. 1925-1934
Near-haploidy and subsequent polyploidization characterize the progressionof peripheral chondrosarcoma
Authors: Bovee, JVMG van Royen, M Bardoel, AFJ Rosenberg, C Cornelisse, CJ Cleton-Jansen, AM Hogendoorn, PCW
Citation: Jvmg. Bovee et al., Near-haploidy and subsequent polyploidization characterize the progressionof peripheral chondrosarcoma, AM J PATH, 157(5), 2000, pp. 1587-1595
Loss of heterozygosity and DNA ploidy point to a diverging genetic mechanism in the origin of peripheral and central chondrosarcoma
Authors: Bovee, JVMG Cleton-Jansen, AM Kuipers-Dijkshoorn, NJ van den Broek, LJCM Taminiau, AHM Cornelisse, CJ Hogendoorn, PCW
Citation: Jvmg. Bovee et al., Loss of heterozygosity and DNA ploidy point to a diverging genetic mechanism in the origin of peripheral and central chondrosarcoma, GENE CHROM, 26(3), 1999, pp. 237-246
Loss of heterozygosity at 11q23.1 and survival in breast cancer: Results of a large European study
Authors: Laake, K Launonen, V Niederacher, D Gudlaugsdottir, S Seitz, S Rio, P Champeme, MH Bieche, I Birnbaum, D White, G Sztan, M Sever, N Plummer, S Osorio, A Broeks, A Huusko, P Spurr, N Borg, A Cleton-Jansen, AM van't Veer, L Benitez, J Casey, G Peterlin, B Olah, E Varley, J Bignon, YJ Scherneck, S Sigurdardottir, V Lidereau, R Eyfjord, J Beckmann, MW Winqvist, R Skovlund, E Borresen-Dale, AL
Citation: K. Laake et al., Loss of heterozygosity at 11q23.1 and survival in breast cancer: Results of a large European study, GENE CHROM, 25(3), 1999, pp. 212-221
Characterization of copine VII, a new member of the copine family, and itsexclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3
Authors: Savino, M d'Apolito, M Centra, M van Beerendonk, HM Cleton-Jansen, AM Whitmore, SA Crawford, J Callen, DF Zelante, L Savoia, A
Citation: M. Savino et al., Characterization of copine VII, a new member of the copine family, and itsexclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3, GENOMICS, 61(2), 1999, pp. 219-226
The PISSLRE gene: Structure, exon skipping, and exclusion as tumor suppressor in breast cancer
Authors: Crawford, J Ianzano, L Savino, M Whitmore, S Cleton-Jansen, AM Settasatian, C d'Apolito, M Seshadri, R Pronk, JC Auerbach, AD Verlander, PC Mathew, CG Tipping, AJ Doggett, NA Zelante, L Callen, DF Savoia, A
Citation: J. Crawford et al., The PISSLRE gene: Structure, exon skipping, and exclusion as tumor suppressor in breast cancer, GENOMICS, 56(1), 1999, pp. 90-97
Genomic structure and expression analysis of the spastic paraplegia gene, SPG7
Authors: Settasatian, C Whitmore, SA Crawford, J Bilton, RL Cleton-Jansen, AM Sutherland, GR Callen, DF
Citation: C. Settasatian et al., Genomic structure and expression analysis of the spastic paraplegia gene, SPG7, HUM GENET, 105(1-2), 1999, pp. 139-144
Molecular detection of minimal residual disease in colorectal and breast cancer
Authors: Liefers, GJ Tollenaar, RAEM Cleton-Jansen, AM
Citation: Gj. Liefers et al., Molecular detection of minimal residual disease in colorectal and breast cancer, HISTOPATHOL, 34(5), 1999, pp. 385-390
Molecular genetic characterization of both components of a dedifferentiated chondrosarcoma, with implications for its histogenesis
Authors: Bovee, JVMG Cleton-Jansen, AM Rosenberg, C Taminiau, AHM Cornelisse, CJ Hogendoorn, PCW
Citation: Jvmg. Bovee et al., Molecular genetic characterization of both components of a dedifferentiated chondrosarcoma, with implications for its histogenesis, J PATHOLOGY, 189(4), 1999, pp. 454-462
Genetic alterations on chromosome 16 and 17 are important features of ductal carcinoma in situ of the breast and are associated with histologic type
Authors: Vos, CBJ ter Haar, NT Rosenberg, C Peterse, JL Cleton-Jansen, AM Cornelisse, CJ van de Vijver, MJ
Citation: Cbj. Vos et al., Genetic alterations on chromosome 16 and 17 are important features of ductal carcinoma in situ of the breast and are associated with histologic type, BR J CANC, 81(8), 1999, pp. 1410-1418
European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables
Authors: Launonen, V Laake, K Huusko, P Niederacher, D Beckmann, MW Barkardottir, RB Geirsdottir, EK Gudmundsson, J Rio, P Bignon, YJ Seitz, S Scherneck, S Bieche, I Champeme, MH Birnbaum, D White, G Varley, J Sztan, M Olah, E Osorio, A Benitez, J Spurr, N Velikonja, N Peterlin, B Borg, A Cleton-Jansen, AM Devilee, P Bloigu, R Lidereau, R Borresen-Dale, AL Winqvist, R
Citation: V. Launonen et al., European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables, BR J CANC, 80(5-6), 1999, pp. 879-882
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3
Authors: Cleton-Jansen, AM Moerland, EW Pronk, JC van Berkel, CGM Apostolou, S Crawford, J Savoia, A Auerbach, AD Mathew, CG Callen, DF Cornelisse, CJ
Citation: Am. Cleton-jansen et al., Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3, BR J CANC, 79(7-8), 1999, pp. 1049-1052
EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas
Authors: Bovee, JVMG Cleton-Jansen, AM Wuyts, W Caethoven, G Taminiau, AHM Bakker, E Van Hul, W Cornelisse, CJ Hogendoorn, PCW
Citation: Jvmg. Bovee et al., EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas, AM J HU GEN, 65(3), 1999, pp. 689-698
Risultati: 1-25 |