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Anne-Marie Cleton-Jansen

Showing results (51-60 of 127) with videos related to

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The Journal of Pathology|March 3, 2004
Molecular analysis of the INK4A/INK4A-ARF gene locus in conventional (central) chondrosarcomas and enchondromas: indication of an important gene for tumour progressionHetty M van Beerendonk, Leida B Rozeman, Antonie H M Taminiau, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 18, 2021
A murine mesenchymal stem cell model for initiating events in osteosarcomagenesis points to CDK4/CDK6 inhibition as a therapeutic targetNatasja Franceschini, Raffaele Gaeta, Paul Krimpenfort, et al.
Biochemical and Biophysical Research Communications|June 5, 2004
Infiltrating leukocytes confound the detection of E-cadherin promoter methylation in tumorsMarcel Lombaerts, Janneke W Middeldorp, Esther van der Weide, et al.
Cancers|April 3, 2021
Transformed Canine and Murine Mesenchymal Stem Cells as a Model for Sarcoma with Complex GenomicsNatasja Franceschini, Bas Verbruggen, Marianna A Tryfonidou, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 9, 2003
A distinct phenotype characterizes tumors from a putative genetic trait involving chondrosarcoma and breast cancer occurring in the same patientAnne-Marie Cleton-Jansen, Michel C Timmerman, Marc J van de Vijver, et al.
Genes, Chromosomes & Cancer|August 3, 2004
Different mechanisms of chromosome 16 loss of heterozygosity in well- versus poorly differentiated ductal breast cancerAnne-Marie Cleton-Jansen, Horst Buerger, Natalja ter Haar, et al.
Histopathology|June 20, 2021
NTRK fusions are extremely rare in bone tumoursSuk Wai Lam, Inge H Briaire-de Bruijn, Tom van Wezel, et al.
The Journal of Molecular Diagnostics : JMD|December 5, 2009
Sensitive and specific KRAS somatic mutation analysis on whole-genome amplified DNA from archival tissuesRonald van Eijk, Marjo van Puijenbroek, Amiet R Chhatta, et al.
Human Mutation|November 4, 2004
Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p.R150CLeida B Rozeman, Luca Sangiorgi, Inge H Briaire-de Bruijn, et al.
The Journal of Pathology|September 1, 2009
Osteosarcoma originates from mesenchymal stem cells in consequence of aneuploidization and genomic loss of Cdkn2Alexander B Mohseny, Karoly Szuhai, Salvatore Romeo, et al.
Pageof 13

Showing results (51-60 of 127) with videos related to

Sort By:
Pageof 13
The Journal of Pathology|March 3, 2004
Molecular analysis of the INK4A/INK4A-ARF gene locus in conventional (central) chondrosarcomas and enchondromas: indication of an important gene for tumour progressionHetty M van Beerendonk, Leida B Rozeman, Antonie H M Taminiau, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 18, 2021
A murine mesenchymal stem cell model for initiating events in osteosarcomagenesis points to CDK4/CDK6 inhibition as a therapeutic targetNatasja Franceschini, Raffaele Gaeta, Paul Krimpenfort, et al.
Biochemical and Biophysical Research Communications|June 5, 2004
Infiltrating leukocytes confound the detection of E-cadherin promoter methylation in tumorsMarcel Lombaerts, Janneke W Middeldorp, Esther van der Weide, et al.
Cancers|April 3, 2021
Transformed Canine and Murine Mesenchymal Stem Cells as a Model for Sarcoma with Complex GenomicsNatasja Franceschini, Bas Verbruggen, Marianna A Tryfonidou, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 9, 2003
A distinct phenotype characterizes tumors from a putative genetic trait involving chondrosarcoma and breast cancer occurring in the same patientAnne-Marie Cleton-Jansen, Michel C Timmerman, Marc J van de Vijver, et al.
Genes, Chromosomes & Cancer|August 3, 2004
Different mechanisms of chromosome 16 loss of heterozygosity in well- versus poorly differentiated ductal breast cancerAnne-Marie Cleton-Jansen, Horst Buerger, Natalja ter Haar, et al.
Histopathology|June 20, 2021
NTRK fusions are extremely rare in bone tumoursSuk Wai Lam, Inge H Briaire-de Bruijn, Tom van Wezel, et al.
The Journal of Molecular Diagnostics : JMD|December 5, 2009
Sensitive and specific KRAS somatic mutation analysis on whole-genome amplified DNA from archival tissuesRonald van Eijk, Marjo van Puijenbroek, Amiet R Chhatta, et al.
Human Mutation|November 4, 2004
Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p.R150CLeida B Rozeman, Luca Sangiorgi, Inge H Briaire-de Bruijn, et al.
The Journal of Pathology|September 1, 2009
Osteosarcoma originates from mesenchymal stem cells in consequence of aneuploidization and genomic loss of Cdkn2Alexander B Mohseny, Karoly Szuhai, Salvatore Romeo, et al.
Pageof 13