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Florent Marguet

Showing results (51-60 of 65) with videos related to

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Journal of Alzheimer'S Disease : JAD|March 26, 2019
Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer's DiseaseEmmanuelle Boscher, Thomas Husson, Olivier Quenez, et al.
Oncotarget|June 22, 2017
Non-invasive detection of somatic mutations using next-generation sequencing in primary central nervous system lymphomaMaxime Fontanilles, Florent Marguet, Élodie Bohers, et al.
Acta Neuropathologica Communications|April 19, 2020
Simultaneous detection of EGFR amplification and EGFRvIII variant using digital PCR-based method in glioblastomaMaxime Fontanilles, Florent Marguet, Philippe Ruminy, et al.
Frontiers in Cell and Developmental Biology|May 3, 2021
Targeting the Urotensin II/UT G Protein-Coupled Receptor to Counteract Angiogenesis and Mesenchymal Hypoxia/Necrosis in GlioblastomaVadim Le Joncour, Pierre-Olivier Guichet, Kleouforo-Paul Dembélé, et al.
Acta Neuropathologica Communications|May 24, 2025
Glioneuronal tumors PATZ1-fused: clinico-molecular and DNA methylation signatures for a variety of morphological and radiological profilesArnault Tauziède-Espariat, Volodia Dangouloff-Ros, Philipp Sievers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 25, 2018
Metabolic causes of nonimmune hydrops fetalis: A next-generation sequencing panel as a first-line investigationBénédicte Sudrié-Arnaud, Florent Marguet, Sophie Patrier, et al.
Clinical Genetics|August 22, 2024
SCYL2-related autosomal recessive neurodevelopmental disorders: Arthrogryposis multiplex congenita-4 and beyond?Marlène Malbos, Gabriella Vera, Harsh Sheth, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 17, 2018
Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's diseaseGaël Nicolas, Rocío Acuña-Hidalgo, Michael J Keogh, et al.
American Journal of Human Genetics|March 21, 2017
Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex CongenitaShifeng Xue, Jérôme Maluenda, Florent Marguet, et al.
Journal of Medical Genetics|April 8, 2022
Overlapping cortical malformations in patients with pathogenic variants in <i>GRIN1</i> and <i>GRIN2B</i>Stefanie Brock, Annie Laquerriere, Florent Marguet, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Journal of Alzheimer'S Disease : JAD|March 26, 2019
Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer's DiseaseEmmanuelle Boscher, Thomas Husson, Olivier Quenez, et al.
Oncotarget|June 22, 2017
Non-invasive detection of somatic mutations using next-generation sequencing in primary central nervous system lymphomaMaxime Fontanilles, Florent Marguet, Élodie Bohers, et al.
Acta Neuropathologica Communications|April 19, 2020
Simultaneous detection of EGFR amplification and EGFRvIII variant using digital PCR-based method in glioblastomaMaxime Fontanilles, Florent Marguet, Philippe Ruminy, et al.
Frontiers in Cell and Developmental Biology|May 3, 2021
Targeting the Urotensin II/UT G Protein-Coupled Receptor to Counteract Angiogenesis and Mesenchymal Hypoxia/Necrosis in GlioblastomaVadim Le Joncour, Pierre-Olivier Guichet, Kleouforo-Paul Dembélé, et al.
Acta Neuropathologica Communications|May 24, 2025
Glioneuronal tumors PATZ1-fused: clinico-molecular and DNA methylation signatures for a variety of morphological and radiological profilesArnault Tauziède-Espariat, Volodia Dangouloff-Ros, Philipp Sievers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 25, 2018
Metabolic causes of nonimmune hydrops fetalis: A next-generation sequencing panel as a first-line investigationBénédicte Sudrié-Arnaud, Florent Marguet, Sophie Patrier, et al.
Clinical Genetics|August 22, 2024
SCYL2-related autosomal recessive neurodevelopmental disorders: Arthrogryposis multiplex congenita-4 and beyond?Marlène Malbos, Gabriella Vera, Harsh Sheth, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 17, 2018
Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's diseaseGaël Nicolas, Rocío Acuña-Hidalgo, Michael J Keogh, et al.
American Journal of Human Genetics|March 21, 2017
Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex CongenitaShifeng Xue, Jérôme Maluenda, Florent Marguet, et al.
Journal of Medical Genetics|April 8, 2022
Overlapping cortical malformations in patients with pathogenic variants in <i>GRIN1</i> and <i>GRIN2B</i>Stefanie Brock, Annie Laquerriere, Florent Marguet, et al.
Pageof 7