Genetic profiling of a distant second glioblastoma multiforme after radiotherapy: recurrence or second primary tumor? (2006)
Nifterik, K.A. Van,
Elkhuizen, P.H.M.,
Andel, R.J. Van,
Stalpers, L.J.A.,
Leenstra, S.,
Lafleur, M.V.M.,
...
Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray (2005)
Ammerlaan, A.C.J.,
Bustos, C. De,
Ararou, A.,
Buckley, P.G.,
Mantripragada, K.K.,
Verstegen, M.J.T.,
...
Amplification of 17p11.2 approximately p12, including PMP22, TOP3A, and MAPK7, in high-grade osteosarcoma (2002)
Dartel, M. Van,
Cornelissen, P.W.A.,
Redeker, S.,
Takkanen, M.,
Knuutila, S.,
Hogendoorn, P.C.W.,
...
Amplification of 17p11.2 approximately p12, including PMP22, TOP3A, and MAPK7, in high-grade osteosarcoma (2002)
Dartel, M. Van,
Cornelissen, P.W.A.,
Redeker, S.,
Takkanen, M.,
Knuutila, S.,
Hogendoorn, P.C.W.,
...
Radiosensitivity and TP 53, EGFR amplification and LOH10 analysis of primary glioma cell cultures (2002)
Gerlach, B.,
Harder, A.H.,
Hulsebos, T.J.M.,
Leenstra, S.,
Slotman, B.J.,
Vandertop, W.P.,
...
Amplification of 17p11.2 approximately p12, including PMP22, TOP3A, and MAPK7, in high-grade osteosarcoma (2002)
Dartel, M. Van,
Cornelissen, P.W.A.,
Redeker, S.,
Takkanen, M.,
Knuutila, S.,
Hogendoorn, P.C.W.,
...
KUB3 amplification and overexpression in human gliomas (2001)
Fischer, U.,
Hemmer, D.,
Heckel, D.G.,
Michel, A.,
Feiden, W.,
...
Limited contribution of interchromosomal gene conversion to NF1 gene mutation (2001)
Luijten, M.,
Fahsold, R.,
Mischung, C.,
Westerveld, A.,
Nurnberg, P.,
Hulsebos, T.J.M.
Duplication and transposition of the NF1 pseudogene regions on chromosomes 2, 14, and 22 (2001)
Luijten, M.,
Redeker, S.,
Minoshima, S.,
Shimizu, N.,
Westerveld, A.,
Hulsebos, T.J.M.
Glioneuronal tumors and medically intractable epilepsy: a clinical study with long-term follow-up of seizure outcome after (2001)
Aronica, E.,
Leenstra, S.,
Rijen, P.C. Van,
Hulsebos, T.J.M.,
Tersmette, A.C.,
...
GOA, a novel gene encoding a ring finger B-box coiled-coil protein, is overexpressed in astrocytoma (2001)
Vandeputte, D.A.A.,
Meije, C.B.,
Dartel, M. Van,
Leenstra, S.,
IJLst-Keizers, H.,
Das, P.K.,
...
GOA, a novel gene encoding a ring finger B-box coiled-coil protein, is overexpressed in astrocytoma (2001)
Vandeputte, D.A.A.,
Meije, C.B.,
Dartel, M. Van,
Leenstra, S.,
IJLst-Keizers, H.,
Das, P.K.,
...
Glioneuronal tumors and medically intractable epilepsy: a clinical study with long-term follow-up of seizure outcome after (2001)
Aronica, E.,
Leenstra, S.,
Rijen, P.C. Van,
Hulsebos, T.J.M.,
Tersmette, A.C.,
...
Glioneuronal tumors and medically intractable epilepsy: a clinical study with long-term follow-up of seizure outcome after (2001)
Aronica, E.,
Leenstra, S.,
Rijen, P.C. Van,
Hulsebos, T.J.M.,
Tersmette, A.C.,
...
GOA, a novel gene encoding a ring finger B-box coiled-coil protein, is overexpressed in astrocytoma (2001)
Vandeputte, D.A.A.,
Meije, C.B.,
Dartel, M. Van,
Leenstra, S.,
IJLst-Keizers, H.,
Das, P.K.,
...
Microsatellite instability and promoter methylation as possible causes of NF1 gene inactivation in neurofibromas (2000)
Luijten, M.,
Redeker, S.,
Noesel, M.M. Van,
Troost, D.,
Westerveld, A.,
Hulsebos, T.J.M.
Cloning, mapping, and expression analysis of a gene encoding a novel mammalian EGF-related protein (SCUBE1) (2000)
Grimmond, S.,
Larder, R.,
Hateren, N. Van,
Siggers, P.,
Hulsebos, T.J.M.,
Arkell, R.,
...
Mechanism of spreading of the highly related neurofibrosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22 (2000)
Luijten, M.,
Wang, Y.P.,
Smith, B.T.,
Westerveld, A.,
Smink, L.J.,
Dunham, I.,
...
Microsatellite instability and promoter methylation as possible causes of NF1 gene inactivation in neurofibromas (2000)
Luijten, M.,
Redeker, S.,
Noesel, M.M. Van,
Troost, D.,
Westerveld, A.,
Hulsebos, T.J.M.
Microsatellite instability and promoter methylation as possible causes of NF1 gene inactivation in neurofibromas (2000)
Luijten, M.,
Redeker, S.,
Noesel, M.M. Van,
Troost, D.,
Westerveld, A.,
Hulsebos, T.J.M.
Microsatellite instability and promoter methylation as possible causes of NF1 gene inactivation in neurofibromas (2000)
Luijten, M.,
Redeker, S.,
Noesel, M.M. Van,
Troost, D.,
Westerveld, A.,
Hulsebos, T.J.M.
Microsatellite instability and promoter methylation as possible causes of NF1 gene inactivation in neurofibromas (2000)
Luijten, M.,
Redeker, S.,
Noesel, M.M. Van,
Troost, D.,
Westerveld, A.,
Hulsebos, T.J.M.
Characterization of the 17p amplicon in human sarcomas: microsatellite marker analysis (1999)
Wolf, M.,
Tarkkanen, M.,
Hulsebos, T.J.M.,
Larramendy, M.L.,
Forus, A.,
Myklebost, O.,
...
Genetic sub-types of human malignant astrocytoma correlate with survival (1998)
Leenstra, S.,
Oskam, N.T.,
Bijleveld, E.H.,
Bosch, D.A.,
Troost, D.,
Hulsebos, T.J.M.
Genetic sub-types of human malignant astrocytoma correlate with survival (1998)
Leenstra, S.,
Oskam, N.T.,
Bijleveld, E.H.,
Bosch, D.A.,
Troost, D.,
Hulsebos, T.J.M.
Malignant astrocytoma-derived region of common amplification in chromosomal band 17p12 is frequently amplified in high-grade osteosarcomas (1997)
Hulsebos, T.J.M.,
Bijleveld, E.H.,
Oskam, N.T.,
Westerveld, A.,
Leenstra, S.,
Hogendoorn, P.C.W.,
...
Cloning of a novel transcription factor-like gene amplified in human glioma including astrocytoma grade I (1997)
Fischer, U.,
Heckel, D.G.,
Michel, A.,
Janka, M.,
Hulsebos, T.J.M.,
Meese, E.
Malignant astrocytoma-derived region of common amplification in chromosomal band 17p12Is frequently amplified in high-grade osteosarcomas (1997)
Hulsebos, T.J.M.,
Bijleveld, E.H.,
Oskam, N.T.,
Westerveld, A.,
Leenstra, S.,
Hogendoorn, P.C.W.,
...
Malignant astrocytoma-derived region of common amplification in chromosomal band 17p12 is frequently amplified in high-grade osteosarcomas (1997)
Hulsebos, T.J.M.,
Bijleveld, E.H.,
Oskam, N.T.,
Westerveld, A.,
Leenstra, S.,
Hogendoorn, P.C.W.,
...
Malignant astrocytoma-derived region of common amplification in chromosomal band 17p12 is frequently amplified in high-grade osteosarcomas (1997)
Hulsebos, T.J.M.,
Bijleveld, E.H.,
Oskam, N.T.,
Westerveld, A.,
Leenstra, S.,
Hogendoorn, P.C.W.,
...
The gene for Hereditary Bullous dystrophy, X-linked Macular Type, maps to the Xq27.3-qter region (1995)
Arwert, F.,
Lungarotti, S.,
Menko, F.H.,
Hulsebos, T.J.M.,
Ropers, H.H.,
...
Identification of the human BetaA2 crystallin gene (CRYBA2): localization of the gene on human chromosome 2 and of the homologous gene on mouse chromosome 1 (1995)
Copeland, N.G.,
Gilbert, D.J.,
Jenkins, N.A.,
Marzella, R.,
Rocchi, M.,
Sinke, R.J.,
...
The Gene for Hereditary Bullous Dystrophy, X-Linked Macular Type, Maps to the Xq27.3-Qter Region (1995)
Arwert, F.,
Lungarotti, M.S.,
Vanoost, B.A.,
Menko, F.H.,
Hulsebos, T.J.M.,
Ropers, H.H.,
...
Long-term survival and transmission of INI1-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndrome
Ammerlaan, A C J,
Ararou, A,
Baas, F,
Tijssen, C C,
...
Rhabdoid tumour predisposition syndrome (RTPS) is a rare syndrome caused by inheritance of a mutated INI1 gene for which only two multigeneration families have been reported. To further characterise...
Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter–22q11.2
Hulsebos, T J M,
Oskam, N T,
Bijleveld, E H,
Westerveld, A,
Hermsen, M A,
...
Ependymomas are glial tumours of the brain and spinal cord. The most frequent genetic change in sporadic ependymoma is monosomy 22, suggesting the presence of an ependymoma tumour suppressor gene on...