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Showing results (821-830 of 839) with videos related to

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Cell|December 26, 2017
Microbiome Influences Prenatal and Adult Microglia in a Sex-Specific MannerMorgane Sonia Thion, Donovan Low, Aymeric Silvin, et al.
Research Square|February 27, 2026
Epigenetic control of microglial developmental milestones from proliferative progenitors to efficient phagocytesAmanda Sierra, Marta Pereira-Iglesias, William Martinson, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Epigenetic control of microglial developmental milestones from proliferative progenitors to efficient phagocytesMarta Pereira-Iglesias, Duncan Martinson, Carles Falco, et al.
Elife|January 17, 2023
Gain-of-function variants in the ion channel gene <i>TRPM3</i> underlie a spectrum of neurodevelopmental disordersLydie Burglen, Evelien Van Hoeymissen, Leila Qebibo, et al.
Cell|February 3, 2024
Microglia maintain structural integrity during fetal brain morphogenesisAkindé René Lawrence, Alice Canzi, Cécile Bridlance, et al.
The American Journal of Tropical Medicine and Hygiene|February 10, 2026
Introducing Minimally Invasive Tissue Sampling to Ascertain Cause of Death in Children and Stillbirths in Central MozambiqueInácio Mandomando, Anélsio Cossa, Augusto Messa, et al.
Orphanet Journal of Rare Diseases|December 14, 2011
Efficacy of vinblastine in central nervous system Langerhans cell histiocytosis: a nationwide retrospective studySophie Ng Wing Tin, Nadine Martin-Duverneuil, Ahmed Idbaih, et al.
Journal of Medical Genetics|November 1, 2022
New insights into <i>CC2D2A</i>-related Joubert syndromeMadeleine Harion, Leila Qebibo, Audrey Riquet, et al.
Clinical Genetics|December 6, 2021
Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication-deletion: Genotype-phenotype correlation for anomalies of the corpus callosumRoseline Vibert, Cyril Mignot, Boris Keren, et al.
Brain : a Journal of Neurology|September 4, 2025
A large cohort study of prenatal exome sequencing redefines diagnosis in fetal corpus callosum anomaliesDelphine Héron, Anna Gerasimenko, Lisa Frugère, et al.
Pageof 84

Showing results (821-830 of 839) with videos related to

Sort By:
Pageof 84
Cell|December 26, 2017
Microbiome Influences Prenatal and Adult Microglia in a Sex-Specific MannerMorgane Sonia Thion, Donovan Low, Aymeric Silvin, et al.
Research Square|February 27, 2026
Epigenetic control of microglial developmental milestones from proliferative progenitors to efficient phagocytesAmanda Sierra, Marta Pereira-Iglesias, William Martinson, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Epigenetic control of microglial developmental milestones from proliferative progenitors to efficient phagocytesMarta Pereira-Iglesias, Duncan Martinson, Carles Falco, et al.
Elife|January 17, 2023
Gain-of-function variants in the ion channel gene <i>TRPM3</i> underlie a spectrum of neurodevelopmental disordersLydie Burglen, Evelien Van Hoeymissen, Leila Qebibo, et al.
Cell|February 3, 2024
Microglia maintain structural integrity during fetal brain morphogenesisAkindé René Lawrence, Alice Canzi, Cécile Bridlance, et al.
The American Journal of Tropical Medicine and Hygiene|February 10, 2026
Introducing Minimally Invasive Tissue Sampling to Ascertain Cause of Death in Children and Stillbirths in Central MozambiqueInácio Mandomando, Anélsio Cossa, Augusto Messa, et al.
Orphanet Journal of Rare Diseases|December 14, 2011
Efficacy of vinblastine in central nervous system Langerhans cell histiocytosis: a nationwide retrospective studySophie Ng Wing Tin, Nadine Martin-Duverneuil, Ahmed Idbaih, et al.
Journal of Medical Genetics|November 1, 2022
New insights into <i>CC2D2A</i>-related Joubert syndromeMadeleine Harion, Leila Qebibo, Audrey Riquet, et al.
Clinical Genetics|December 6, 2021
Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication-deletion: Genotype-phenotype correlation for anomalies of the corpus callosumRoseline Vibert, Cyril Mignot, Boris Keren, et al.
Brain : a Journal of Neurology|September 4, 2025
A large cohort study of prenatal exome sequencing redefines diagnosis in fetal corpus callosum anomaliesDelphine Héron, Anna Gerasimenko, Lisa Frugère, et al.
Pageof 84