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Nicolas Goudin

Showing results (41-50 of 55) with videos related to

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Science Advances|October 17, 2025
Kinesin-1 coordinates cross-talk between microtubule and actin cytoskeletons during dendritic cell migrationPierre Duquesne, Céline Aoun, Mathieu Kurowska, et al.
The Journal of Clinical Investigation|June 6, 2024
PIK3CA inhibition in models of proliferative glomerulonephritis and lupus nephritisJunna Yamaguchi, Pierre Isnard, Noémie Robil, et al.
American Journal of Human Genetics|December 5, 2017
Mutations in TUBB4B Cause a Distinctive Sensorineural DiseaseRomain Luscan, Sabrina Mechaussier, Antoine Paul, et al.
Blood Cancer Journal|November 5, 2025
Telomere occupancy by TRF2 is altered by KIT mutations and correlates with mastocytosis regressionJulie Bruneau, Sophie Georgin-Lavialle, Sophia Ladraa, et al.
Haematologica|October 15, 2020
XPO1 regulates erythroid differentiation and is a new target for the treatment of β-thalassemiaFlavia Guillem, Michaël Dussiot, Elia Colin, et al.
The Journal of Experimental Medicine|September 15, 2023
Hemifacial myohyperplasia is due to somatic muscular PIK3CA gain-of-function mutations and responds to pharmacological inhibitionCharles Bayard, Eleonora Segna, Maxime Taverne, et al.
Signal Transduction and Targeted Therapy|June 16, 2024
Targeted therapy for capillary-venous malformationsLola Zerbib, Sophia Ladraa, Antoine Fraissenon, et al.
Science Advances|December 9, 2022
PIK3CA gain-of-function mutation in adipose tissue induces metabolic reprogramming with Warburg-like effect and severe endocrine disruptionSophia Ladraa, Lola Zerbib, Charles Bayard, et al.
The Journal of Experimental Medicine|June 21, 2019
Severe influenza pneumonitis in children with inherited TLR3 deficiencyHye Kyung Lim, Sarah X L Huang, Jie Chen, et al.
American Journal of Human Genetics|August 1, 2017
Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal EncephalopathyFlorence Habarou, Yamina Hamel, Tobias B Haack, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Science Advances|October 17, 2025
Kinesin-1 coordinates cross-talk between microtubule and actin cytoskeletons during dendritic cell migrationPierre Duquesne, Céline Aoun, Mathieu Kurowska, et al.
The Journal of Clinical Investigation|June 6, 2024
PIK3CA inhibition in models of proliferative glomerulonephritis and lupus nephritisJunna Yamaguchi, Pierre Isnard, Noémie Robil, et al.
American Journal of Human Genetics|December 5, 2017
Mutations in TUBB4B Cause a Distinctive Sensorineural DiseaseRomain Luscan, Sabrina Mechaussier, Antoine Paul, et al.
Blood Cancer Journal|November 5, 2025
Telomere occupancy by TRF2 is altered by KIT mutations and correlates with mastocytosis regressionJulie Bruneau, Sophie Georgin-Lavialle, Sophia Ladraa, et al.
Haematologica|October 15, 2020
XPO1 regulates erythroid differentiation and is a new target for the treatment of β-thalassemiaFlavia Guillem, Michaël Dussiot, Elia Colin, et al.
The Journal of Experimental Medicine|September 15, 2023
Hemifacial myohyperplasia is due to somatic muscular PIK3CA gain-of-function mutations and responds to pharmacological inhibitionCharles Bayard, Eleonora Segna, Maxime Taverne, et al.
Signal Transduction and Targeted Therapy|June 16, 2024
Targeted therapy for capillary-venous malformationsLola Zerbib, Sophia Ladraa, Antoine Fraissenon, et al.
Science Advances|December 9, 2022
PIK3CA gain-of-function mutation in adipose tissue induces metabolic reprogramming with Warburg-like effect and severe endocrine disruptionSophia Ladraa, Lola Zerbib, Charles Bayard, et al.
The Journal of Experimental Medicine|June 21, 2019
Severe influenza pneumonitis in children with inherited TLR3 deficiencyHye Kyung Lim, Sarah X L Huang, Jie Chen, et al.
American Journal of Human Genetics|August 1, 2017
Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal EncephalopathyFlorence Habarou, Yamina Hamel, Tobias B Haack, et al.
Pageof 6