Search research articles
Contact Us
Filters
Showing results (51-60 of 127) with videos related to
Page
of 13
Sort By:
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 progression
Hetty 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 target
Natasja 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 tumors
Marcel 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 Genomics
Natasja 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 patient
Anne-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 cancer
Anne-Marie Cleton-Jansen, Horst Buerger, Natalja ter Haar, et al.
Histopathology
|
June 20, 2021
NTRK fusions are extremely rare in bone tumours
Suk 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 tissues
Ronald 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.R150C
Leida 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 Cdkn2
Alexander B Mohseny, Karoly Szuhai, Salvatore Romeo, et al.
Page
of 13
Search research articles
Search
Showing results (51-60 of 127) with videos related to
Sort By:
Page
of 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 progression
Hetty 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 target
Natasja 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 tumors
Marcel 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 Genomics
Natasja 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 patient
Anne-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 cancer
Anne-Marie Cleton-Jansen, Horst Buerger, Natalja ter Haar, et al.
Histopathology
|
June 20, 2021
NTRK fusions are extremely rare in bone tumours
Suk 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 tissues
Ronald 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.R150C
Leida 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 Cdkn2
Alexander B Mohseny, Karoly Szuhai, Salvatore Romeo, et al.
Page
of 13