T. Hulsebos

发表

Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria

A. Stemmer-Rachamimov, B. Korf, D. Evans, 2013, American journal of medical genetics. Part A.

Genetic profiling of a distant second glioblastoma multiforme after radiotherapy: Recurrence or second primary tumor?

W. Vandertop, S. Leenstra, P. Sminia, 2006, Journal of neurosurgery.

Amplification of 17p11.2∼p12, including PMP22, TOP3A, and MAPK7, in high-grade osteosarcoma

S. Knuutila, P. Hogendoorn, A. Westerveld, 2002 .

Amplification of 17p11.2 approximately p12, including PMP22, TOP3A, and MAPK7, in high-grade osteosarcoma.

S. Knuutila, P. Hogendoorn, A. Westerveld, 2002, Cancer genetics and cytogenetics.

Focal Chromosomal Copy Number Aberrations Identify CMTM8 and GPR177 as New Candidate Driver Genes in Osteosarcoma

F. Baas, B. Ylstra, O. Krijgsman, 2014, PloS one.

Expanding the mutational spectrum of LZTR1 in schwannomatosis

S. Nelson, M. Giovannini, M. Benelli, 2014, European Journal of Human Genetics.

The Molecular Genetics of Schwannomatosis

T. Hulsebos, 2009 .

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.

F. Baas, P. Barth, P. Bolhuis, 1991, American journal of human genetics.

Screening for germ‐line mutations in the NF2 Gene

K. Hoang-Xuan, G. Thomas, M. Sanson, 1995, Genes, chromosomes & cancer.

Predominant occurrence of somatic mutations of the NF2 gene in meningiomas and schwannomas

X. Estivill, K. Hoang-Xuan, G. Thomas, 1995, Genes, chromosomes & cancer.

Premature termination of SMARCB1 translation may be followed by reinitiation in schwannomatosis-associated schwannomas, but results in absence of SMARCB1 expression in rhabdoid tumors

F. Baas, P. Wesseling, W. Verhagen, 2014, Acta Neuropathologica.

Long-term survival and transmission of INI1-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndrome

F. Baas, P. Wesseling, C. Tijssen, 2007, British Journal of Cancer.

A region of common deletion in 22q13.3 in human glioma associated with astrocytoma progression

T. Hulsebos, E. Bijleveld, N. Oskam, 2000, International journal of cancer.

Dynamics of genetic alterations associated with glioma recurrence

S. Leenstra, D. Troost, T. Hulsebos, 1998, Genes, chromosomes & cancer.

Molecular characterization of chromosome 22 deletions in schwannomas

E. Bijlsma, A. Westerveld, D. Bosch, 1992, Genes, Chromosomes and Cancer.

Molecular analysis of genetic changes in ependymomas

G. Thomas, D. Troost, E. Bijlsma, 1995, Genes, chromosomes & cancer.

Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri

F. Baas, I. Christiaans, P. V. D. Munckhof, 2011, neurogenetics.

Myxoid epithelioid sarcoma: a diagnostic challenge. A report on six cases

T. Mentzel, J. V. van Krieken, U. Flucke, 2010, Histopathology.

Overexpression through amplification of genes in chromosome region 17p11.2∼p12 in high-grade osteosarcoma

M. Kool, S. Redeker, T. Hulsebos, 2004 .

Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22

B. Roe, I. Dunham, L. Smink, 2000, European Journal of Human Genetics.

Oncogenic Properties of Candidate Oncogenes in Chromosome Region 17p11.2p12 in Human Osteosarcoma

F. Baas, T. Hulsebos, J. Both, 2016, Cytogenetic and Genome Research.

glioblastomas display improved survival and reduced NADP + -dependent IDH activity ex vivo

M. Kool, S. Leenstra, D. Troost, 2009 .

Secondary meningioma in a long-term survivor of atypical teratoid/rhabdoid tumour with a germline INI1 mutation

P. Wesseling, C. Tijssen, M. Houben, 2008, Child's Nervous System.

Type 1 papillary renal cell carcinoma in a patient with schwannomatosis: Mosaic versus loss of SMARCB1 expression in respectively schwannoma and renal tumor cells

F. Baas, P. Wesseling, A. V. D. van den Ouweland, 2016, Genes, chromosomes & cancer.

SMARCB1 Involvement in the Development of Leiomyoma in a Patient With Schwannomatosis

P. Wesseling, V. Hans, U. Flucke, 2014, The American journal of surgical pathology.

Identification and Characterization of the In Vitro Synthesized Gene Products of Bacteriophage M 13

R. Konings, C. A. Hondel, T. Hulsebos, 2003 .

Polyposis coli, craniofacial exostosis and astrocytoma: the concomitant occurrence of the Gardner's and Turcot syndromes.

J. V. van Overbeeke, T. Hulsebos, R. Koot, 1996, Surgical neurology.

Analysis of mutations in the SCH gene in schwannomas

G. Thomas, O. Delattre, E. Bijlsma, 1994, Genes, chromosomes & cancer.

Identification of the human beta A2 crystallin gene (CRYBA2): localization of the gene on human chromosome 2 and of the homologous gene on mouse chromosome 1.

M. Rocchi, R. Sinke, N. Copeland, 1995, Genomics.

The beta crystallin genes on human chromosome 22 define a new region of homology with mouse chromosome 5.

N. Copeland, D. Gilbert, N. Jenkins, 1995, Genomics.

Mutational profiling of kinases in glioblastoma

Dirk Troost, Sieger Leenstra, W. Vandertop, 2014, BMC Cancer.

The combination of IDH1 mutations and MGMT methylation status predicts survival in glioblastoma better than either IDH1 or MGMT alone.

Pieter Wesseling, Dirk Troost, Dagmar Verbaan, 2014, Neuro-oncology.

The combination of IDH 1 mutations and MGMT methylation status predicts survival in glioblastoma better than either IDH 1 or MGMT alone

W. Vandertop, S. Leenstra, D. Troost, 2014 .

Limited contribution of interchromosomal gene conversion toNF1 gene mutation

P. Nürnberg, R. Fahsold, C. Mischung, 2001, Journal of medical genetics.

Cloning of a novel transcription factor-like gene amplified in human glioma including astrocytoma grade I.

U. Fischer, E. Meese, D. Heckel, 1997, Human molecular genetics.

KUB3 amplification and overexpression in human gliomas

U. Fischer, E. Meese, W. Feiden, 2001, Glia.

Microsatellite instability and promoter methylation as possible causes of NF1 gene inactivation in neurofibromas

D. Troost, M. Luijten, A. Westerveld, 2000, European Journal of Human Genetics.

Germline mutation of INI1/SMARCB1 in familial schwannomatosis.

F. Baas, P. Wesseling, A. Plomp, 2007, American journal of human genetics.

Fine mapping of a region of common deletion on chromosome arm 10p in human glioma

A. Westerveld, T. Hulsebos, E. Bijleveld, 1997, Genes, chromosomes & cancer.

Glioneuronal tumors and medically intractable epilepsy: a clinical study with long-term follow-up of seizure outcome after surgery

E. Aronica, B. Yankaya, S. Leenstra, 2001, Epilepsy Research.

IDH1 mutations at residue p.R132 (IDH1R132) occur frequently in high‐grade gliomas but not in other solid tumors

A. Marchetti, F. Buttitta, W. Vandertop, 2009, Human mutation.

Isolation and characterization of alphoid DNA sequences specific for the pericentric regions of chromosomes 4, 5, 9, and 19.

H. Ropers, B. Wieringa, H H Ropers, 1988, Cytogenetics and cell genetics.

Nucleotide sequence of the filamentous bacteriophage M13 DNA genome: comparison with phage fd.

P M van Wezenbeek, T J Hulsebos, J G Schoenmakers, 1980, Gene.

Localization of a putative low‐penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling‐path genomic microarray

J. Dumanski, K. Mantripragada, P. Buckley, 2005, Genes, chromosomes & cancer.

Duplication and transposition of the NF1 pseudogene regions on chromosomes 2, 14, and 22

S. Minoshima, N. Shimizu, M. Luijten, 2001, Human Genetics.

GOA, a novel gene encoding a ring finger B-box coiled-coil protein, is overexpressed in astrocytoma.

F. Baas, S. Leenstra, D. Troost, 2001, Biochemical and biophysical research communications.

Identification of Novel Candidate Oncogenes in Chromosome Region 17p11.2-p12 in Human Osteosarcoma

F. Baas, G. Schaap, T. Hulsebos, 2012, PloS one.

Infrequent but high-level amplification of 17p11.2∼p12 in human glioma

S. Leenstra, D. Troost, T. Hulsebos, 2003 .

Characterization of the 17p amplicon in human sarcomas: microsatellite marker analysis.

L. Aaltonen, O. Myklebost, S. Knuutila, 1997, International journal of cancer.

Amplification and overexpression of genes in 17p11.2 ~ p12 in osteosarcoma.

T. Hulsebos, M. van Dartel, 2004, Cancer genetics and cytogenetics.

Characterization of PMP22 expression in osteosarcoma.

T. Hulsebos, M. van Dartel, 2004, Cancer genetics and cytogenetics.

Overexpression through amplification of genes in chromosome region 17p11.2 approximately p12 in high-grade osteosarcoma.

M. Kool, S. Redeker, T. Hulsebos, 2004, Cancer genetics and cytogenetics.

Characterization of the 17p amplicon in human sarcomas: Microsatellite marker analysis

L. Aaltonen, O. Myklebost, S. Knuutila, 1999 .

Malignant astrocytoma‐derived region of common amplification in chromosomal band 17p12 is frequently amplified in high‐grade osteosarcomas

S. Leenstra, P. Hogendoorn, A. Westerveld, 1997, Genes, chromosomes & cancer.

Amplification of the anonymous marker D17S67 in malignant astrocytomas

S. Leenstra, E. Bijlsma, A. Westerveld, 1994, Genes, chromosomes & cancer.

Genetic and cytogenetic analysis of the “Th-Ps” region of the Y chromosome of Drosophila hydei: evidence for dual functions of the lampbrush loop-forming fertility genes?

J. Hackstein, T. Hulsebos, K. H. Glätzer, 1991, Molecular and General Genetics MGG.

Lampbrush loop-specific protein of Drosophila hydei.

J. Hackstein, W. Hennig, T. Hulsebos, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Involvement of Y chromosomal loci in the synthesis of Drosophila hydei sperm proteins.

J. Hackstein, W. Hennig, T. Hulsebos, 1983, Developmental biology.

Regulation of Structural Sperm Protein Synthesis by Y Chromosomal Loci

J. Hackstein, W. Hennig, T. Hulsebos, 1982 .

Absence of AKT 1 mutations in glioblastoma

W. Vandertop, S. Leenstra, A. Bardelli, 2017 .

Absence of AKT1 Mutations in Glioblastoma

Dirk Troost, W. Peter Vandertop, Sieger Leenstra, 2009, PloS one.

UvA-DARE ( Digital Academic Repository ) Absence of AKT 1 Mutations in Glioblastoma

Dirk, W. Vandertop, S. Leenstra, 2009 .

Synchronous Hodgkin’s lymphoma and schwannomas mimicking refractory Hodgkin’s lymphoma

R. Haas, O. Leeksma, A. Rivière, 2015, Annals of Hematology.

Radiosensitivity and TP53, EGFR Amplification and LOH10 Analysis of Primary Glioma Cell Cultures

W. Vandertop, S. Leenstra, P. Sminia, 2002, Strahlentherapie und Onkologie.

Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri

F. Baas, I. Christiaans, S. Kenter, 2012, neurogenetics.

Genetic and physical demarcation of the locus for dystrophia myotonica.

H. Ropers, B. Wieringa, T. Hulsebos, 1988, Advances in neurology.

Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas

F. Baas, P. van den Munckhof, I. Christiaans, 2010, Journal of Medical Genetics.

The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region.

G. Pals, B. V. van Oost, M. Ligtenberg, 1995, American Journal of Human Genetics.

Molecular characterization of areas with low grade tumor or satellitosis in human malignant astrocytomas.

S. Leenstra, D. Troost, A. Westerveld, 1992, Cancer research.

Allele loss on chromosomes 10 and 17p and epidermal growth factor receptor gene amplification in human malignant astrocytoma related to prognosis.

S. Leenstra, D. Troost, E. Bijlsma, 1994, British Journal of Cancer.

Regional fine mapping of the β crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2

G. Thomas, O. Delattre, J. Dumanski, 1993, Genes, chromosomes & cancer.

Differential radiosensitizing potential of temozolomide in MGMT promoter methylated glioblastoma multiforme cell lines.

S. Leenstra, P. Sminia, L. Stalpers, 2007, International journal of radiation oncology, biology, physics.

Re: Infrequent SMARCB1/INI1 gene alteration in epithelioid sarcoma: a useful tool in distinguishing epithelioid sarcoma from malignant rhabdoid tumor: Direct evidence of mutational inactivation of SMARCB1/INI1 in epithelioid sarcoma.

Uta Flucke, Pieter J Slootweg, Thomas Mentzel, 2009, Human pathology.

Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5.

I. Dunham, G. Thomas, O. Delattre, 1995, Genomics.

Molecular analysis in patients with mucopolysaccharidosis type II suggests that DXS466 maps within the Hunter gene

E. Schwinger, J. Hopwood, A. Gal, 1993, Human Genetics.

Molecular-genetic characterisation of gliomas that recur as same grade or higher grade tumours

S. Leenstra, D. Troost, T. Hulsebos, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

New distal marker closely linked to the fragile X locus

A. Smits, A. Westerveld, S. Broersen, 1991, Human Genetics.

A. Ouweland, B. Hamel, M. Hermsen, 2022 .

Direct assignment of the human βB2 and βB3 crystallin genes to 22q11.2→q12: markers for neurofibromatosis 2

R. Brakenhoff, E. Bijlsma, A. Westerveld, 1991 .

Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spots.

H. Brunner, B. Hamel, T. Hulsebos, 1993, American journal of medical genetics.

Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosome.

R. Hochstenbach, H. Ropers, F. Oerlemans, 1986, Cytogenetics and cell genetics.

Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathy

H. Brunner, B. Wieringa, F. Spaans, 1991, Neurology.

EcoRI RFLP at 19 cen-q13.2 identified by the anonymous DNA sequence pPM6.7 (D19S18).

J. Bril, H. Ropers, B. Wieringa, 1987, Nucleic acids research.

Isolation of a polymorphic DNA sequence pJSB11 (D19S16) from the human chromosome 19cen-q13.2 region linked to the myotonic dystrophy (DM) gene.

B. Wieringa, J. Schepens, H. Smeets, 1987, Nucleic acids research.

A locus at 19cen-19q13.2 (D19S15) containing three RFLPs linked to myotonic dystrophy (DM) is recognized by probe pJSB6.

H. Ropers, B. Wieringa, J. Schepens, 1987, Nucleic acids research.

pHW60, an anonymous single copy clone from the proximal portion of the long arm of chromosome 19 (HGM8 assignment no. D19S13).

B. Wieringa, M. Coerwinkel, R. Peek, 1986, Nucleic acids research.

Infrequent but high-level amplification of 17p11.2 approximately p12 in human glioma.

S. Leenstra, D. Troost, T. Hulsebos, 2003, Cancer genetics and cytogenetics.

Identification and characterization of the in vitro synthesized gene products of bacteriophage M13

R. Konings, C. A. van den Hondel, T. Hulsebos, 1975, Journal of virology.

Nucleotide sequence of gene VII and of a hypothetical gene (IX) in bacteriophage M13.

J. Schoenmakers, T. Hulsebos, 1978, Nucleic acids research.

The nucleotide sequence of several genes and regulatory elements on the bacteriophage M 13 genome

T. Hulsebos, 1980 .

recur as same grade or higher grade tumours Molecular-genetic characterisation of gliomas that

S. Leenstra, D. Troost, T. Hulsebos, 2006 .

Neurofibromatosis type 1: mutational mechanisms and pseudogenes and pseudogenes

D. Troost, M. Luijten, A. Westerveld, 2001 .

Genetic sub‐types of human malignant astrocytoma correlate with survival

S. Leenstra, D. Troost, D. Bosch, 1998, International journal of cancer.

SMARCB1/INI1 maternal germ line mosaicism in schwannomatosis

F. Baas, M. Delatycki, M. Jakobs, 2010, Clinical genetics.

Cloning, mapping, and expression analysis of a gene encoding a novel mammalian EGF-related protein (SCUBE1).

S. Grimmond, R. Arkell, A. Greenfield, 2000, Genomics.

Limited contribution of interchromosomal gene conversion toNF1 gene mutation

C. Mischung, T. Hulsebos, Andries Westerveld, 2001, Journal of medical genetics.

SMARCB1 Involvement in the Development of Leiomyoma in a Patient With Schwannomatosis

P. Wesseling, V. Hans, U. Flucke, 2014, The American journal of surgical pathology.

SMARCB1/INI1 maternal germ line mosaicism in schwannomatosis

F. Baas, M. Delatycki, M. Jakobs, 2010, Clinical genetics.