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M Raynaud

Showing results (51-60 of 64) with videos related to

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Neurogenetics|October 20, 2005
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosisK Poirier, D Lacombe, B Gilbert-Dussardier, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|August 19, 2009
Differential expression of biomarkers in primary non-small cell lung cancer and metastatic sitesCarlos Gomez-Roca, Christophe M Raynaud, Frederique Penault-Llorca, et al.
Clinical Genetics|January 7, 2011
Twenty-five novel mutations including duplications in the ATP7A geneM-P Moizard, N Ronce, S Blesson, et al.
International Journal of Cancer|August 21, 2010
Tumor associated mesenchymal stem cells protects ovarian cancer cells from hyperthermia through CXCL12Raphael Lis, Cyril Touboul, Pejman Mirshahi, et al.
Journal of Experimental & Clinical Cancer Research : CR|June 11, 2022
The immune landscape of solid pediatric tumorsShimaa Sherif, Jessica Roelands, William Mifsud, et al.
Molecular Psychiatry|February 25, 2009
Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autismF Laumonnier, C Shoubridge, C Antar, et al.
Journal of Proteome Research|June 6, 2013
Adaptation of a commonly used, chemically defined medium for human embryonic stem cells to stable isotope labeling with amino acids in cell cultureAlbert R Liberski, Muna N Al-Noubi, Zahra H Rahman, et al.
Frontiers in Oncology|February 23, 2026
Enhancing the accuracy of molecular classification of pediatric CNS tumors: a dual-classifier approach using DNA methylation profilingEsra Moosa, Rania Alanany, Shimaa Sherif, et al.
Behavior Genetics|January 12, 2013
Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French familiesM Huc-Chabrolle, C Charon, A Guilmatre, et al.
The Journal of Allergy and Clinical Immunology|May 16, 2024
Loss of the TRPM4 channel in humans causes immune dysregulation with defective monocyte migrationFang Yu, Satanay Hubrack, Christophe M Raynaud, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Neurogenetics|October 20, 2005
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosisK Poirier, D Lacombe, B Gilbert-Dussardier, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|August 19, 2009
Differential expression of biomarkers in primary non-small cell lung cancer and metastatic sitesCarlos Gomez-Roca, Christophe M Raynaud, Frederique Penault-Llorca, et al.
Clinical Genetics|January 7, 2011
Twenty-five novel mutations including duplications in the ATP7A geneM-P Moizard, N Ronce, S Blesson, et al.
International Journal of Cancer|August 21, 2010
Tumor associated mesenchymal stem cells protects ovarian cancer cells from hyperthermia through CXCL12Raphael Lis, Cyril Touboul, Pejman Mirshahi, et al.
Journal of Experimental & Clinical Cancer Research : CR|June 11, 2022
The immune landscape of solid pediatric tumorsShimaa Sherif, Jessica Roelands, William Mifsud, et al.
Molecular Psychiatry|February 25, 2009
Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autismF Laumonnier, C Shoubridge, C Antar, et al.
Journal of Proteome Research|June 6, 2013
Adaptation of a commonly used, chemically defined medium for human embryonic stem cells to stable isotope labeling with amino acids in cell cultureAlbert R Liberski, Muna N Al-Noubi, Zahra H Rahman, et al.
Frontiers in Oncology|February 23, 2026
Enhancing the accuracy of molecular classification of pediatric CNS tumors: a dual-classifier approach using DNA methylation profilingEsra Moosa, Rania Alanany, Shimaa Sherif, et al.
Behavior Genetics|January 12, 2013
Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French familiesM Huc-Chabrolle, C Charon, A Guilmatre, et al.
The Journal of Allergy and Clinical Immunology|May 16, 2024
Loss of the TRPM4 channel in humans causes immune dysregulation with defective monocyte migrationFang Yu, Satanay Hubrack, Christophe M Raynaud, et al.
Pageof 7