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Pascal Vannuffel

Showing results (1-10 of 6) with videos related to

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Molecular Genetics and Metabolism|February 9, 2010
Identification and characterization of a novel homozygous deletion in the alpha-N-acetylglucosaminidase gene in a patient with Sanfilippo type B syndrome (mucopolysaccharidosis IIIB)Kristen J Champion, Monica J Basehore, Tim Wood, et al.
American Journal of Human Genetics|June 15, 2007
The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onsetIsabelle Maystadt, René Rezsöhazy, Martine Barkats, et al.
British Journal of Haematology|September 22, 2009
Impaired up-regulation of polo-like kinase 2 in B-cell chronic lymphocytic leukaemia lymphocytes resistant to fludarabine and 2-chlorodeoxyadenosine: a potential marker of defective damage responseEmeline de Viron, Laurent Knoops, Thierry Connerotte, et al.
Virchows Archiv : an International Journal of Pathology|March 16, 2024
Multicenter evaluation of an automated, multiplex, RNA-based molecular assay for detection of ALK, ROS1, RET fusions and MET exon 14 skipping in NSCLCLinea Melchior, Astrid Hirschmann, Paul Hofman, et al.
British Journal of Haematology|October 18, 2005
Activity and safety of combined rituximab with chlorambucil in patients with mantle cell lymphomaDeborah Bauwens, Marie Maerevoet, Lucienne Michaux, et al.
Genes, Chromosomes & Cancer|July 8, 2009
Improved detection of chromosomal abnormalities in chronic lymphocytic leukemia by conventional cytogenetics using CpG oligonucleotide and interleukin-2 stimulation: A Belgian multicentric studyNatalie Put, Peter Konings, Katrina Rack, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Molecular Genetics and Metabolism|February 9, 2010
Identification and characterization of a novel homozygous deletion in the alpha-N-acetylglucosaminidase gene in a patient with Sanfilippo type B syndrome (mucopolysaccharidosis IIIB)Kristen J Champion, Monica J Basehore, Tim Wood, et al.
American Journal of Human Genetics|June 15, 2007
The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onsetIsabelle Maystadt, René Rezsöhazy, Martine Barkats, et al.
British Journal of Haematology|September 22, 2009
Impaired up-regulation of polo-like kinase 2 in B-cell chronic lymphocytic leukaemia lymphocytes resistant to fludarabine and 2-chlorodeoxyadenosine: a potential marker of defective damage responseEmeline de Viron, Laurent Knoops, Thierry Connerotte, et al.
Virchows Archiv : an International Journal of Pathology|March 16, 2024
Multicenter evaluation of an automated, multiplex, RNA-based molecular assay for detection of ALK, ROS1, RET fusions and MET exon 14 skipping in NSCLCLinea Melchior, Astrid Hirschmann, Paul Hofman, et al.
British Journal of Haematology|October 18, 2005
Activity and safety of combined rituximab with chlorambucil in patients with mantle cell lymphomaDeborah Bauwens, Marie Maerevoet, Lucienne Michaux, et al.
Genes, Chromosomes & Cancer|July 8, 2009
Improved detection of chromosomal abnormalities in chronic lymphocytic leukemia by conventional cytogenetics using CpG oligonucleotide and interleukin-2 stimulation: A Belgian multicentric studyNatalie Put, Peter Konings, Katrina Rack, et al.
Pageof 1