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Dominique Vidaud

Showing results (61-70 of 90) with videos related to

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Human Molecular Genetics|September 11, 2012
Somatic NF1 inactivation is a frequent event in sporadic pheochromocytomaNelly Burnichon, Alexandre Buffet, Béatrice Parfait, et al.
Neuro-Oncology|February 7, 2018
Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosisCamille Louvrier, Eric Pasmant, Audrey Briand-Suleau, et al.
Journal of Human Genetics|January 30, 2015
NF1 single and multi-exons copy number variations in neurofibromatosis type 1Apolline Imbard, Eric Pasmant, Audrey Sabbagh, et al.
The Journal of Molecular Diagnostics : JMD|November 26, 2023
Droplet Digital PCR for Fast and Accurate Characterization of NF1 Locus Deletions: Confirmation of the Predominant Maternal Origin of Type-1 DeletionsLaurence Pacot, Manuela Ye, Juliette Nectoux, et al.
BMC Genomics|July 16, 2013
MicroRNAome profiling in benign and malignant neurofibromatosis type 1-associated nerve sheath tumors: evidences of PTEN pathway alterations in early NF1 tumorigenesisJulien Masliah-Planchon, Eric Pasmant, Armelle Luscan, et al.
Sarcoma|September 5, 2008
Frequent EGFR Positivity and Overexpression in High-Grade Areas of Human MPNSTsSéverine Tabone-Eglinger, Radislav Bahleda, Jean-François Côté, et al.
Journal of the National Cancer Institute|October 29, 2011
Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1Eric Pasmant, Audrey Sabbagh, Julien Masliah-Planchon, et al.
Clinical Chemistry and Laboratory Medicine|April 4, 2018
Non-invasive prenatal diagnosis of paternally inherited disorders from maternal plasma: detection of NF1 and CFTR mutations using droplet digital PCRAurélia Gruber, Mathilde Pacault, Laila Allach El Khattabi, et al.
Journal of Medical Genetics|September 29, 2023
Neurofibromatosis type 1 mosaicism in patients with constitutional mismatch repair deficiencyLéa Guerrini-Rousseau, Eric Pasmant, Martine Muleris, et al.
NPJ Genomic Medicine|September 8, 2024
Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaicsLaurence Pacot, Dominique Vidaud, Manuela Ye, et al.
Pageof 9

Showing results (61-70 of 90) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|September 11, 2012
Somatic NF1 inactivation is a frequent event in sporadic pheochromocytomaNelly Burnichon, Alexandre Buffet, Béatrice Parfait, et al.
Neuro-Oncology|February 7, 2018
Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosisCamille Louvrier, Eric Pasmant, Audrey Briand-Suleau, et al.
Journal of Human Genetics|January 30, 2015
NF1 single and multi-exons copy number variations in neurofibromatosis type 1Apolline Imbard, Eric Pasmant, Audrey Sabbagh, et al.
The Journal of Molecular Diagnostics : JMD|November 26, 2023
Droplet Digital PCR for Fast and Accurate Characterization of NF1 Locus Deletions: Confirmation of the Predominant Maternal Origin of Type-1 DeletionsLaurence Pacot, Manuela Ye, Juliette Nectoux, et al.
BMC Genomics|July 16, 2013
MicroRNAome profiling in benign and malignant neurofibromatosis type 1-associated nerve sheath tumors: evidences of PTEN pathway alterations in early NF1 tumorigenesisJulien Masliah-Planchon, Eric Pasmant, Armelle Luscan, et al.
Sarcoma|September 5, 2008
Frequent EGFR Positivity and Overexpression in High-Grade Areas of Human MPNSTsSéverine Tabone-Eglinger, Radislav Bahleda, Jean-François Côté, et al.
Journal of the National Cancer Institute|October 29, 2011
Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1Eric Pasmant, Audrey Sabbagh, Julien Masliah-Planchon, et al.
Clinical Chemistry and Laboratory Medicine|April 4, 2018
Non-invasive prenatal diagnosis of paternally inherited disorders from maternal plasma: detection of NF1 and CFTR mutations using droplet digital PCRAurélia Gruber, Mathilde Pacault, Laila Allach El Khattabi, et al.
Journal of Medical Genetics|September 29, 2023
Neurofibromatosis type 1 mosaicism in patients with constitutional mismatch repair deficiencyLéa Guerrini-Rousseau, Eric Pasmant, Martine Muleris, et al.
NPJ Genomic Medicine|September 8, 2024
Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaicsLaurence Pacot, Dominique Vidaud, Manuela Ye, et al.
Pageof 9