Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Daniel Medina-Cano

Showing results (1-10 of 10) with videos related to

Pageof 1
Sort By:
Development (Cambridge, England)|July 28, 2022
Rapid and robust directed differentiation of mouse epiblast stem cells into definitive endoderm and forebrain organoidsDaniel Medina-Cano, Emily K Corrigan, Rachel A Glenn, et al.
Developmental Cell|August 28, 2025
A mouse organoid platform for modeling cerebral cortex development and cis-regulatory evolution in vitroDaniel Medina-Cano, Mohammed T Islam, Veronika Petrova, et al.
Developmental Cell|August 20, 2025
Enhancer remodeling by OTX2 directs specification and patterning of mammalian definitive endodermLy-Sha Ee, Daniel Medina-Cano, Emily Goetzler, et al.
Elife|October 13, 2018
High N-glycan multiplicity is critical for neuronal adhesion and sensitizes the developing cerebellum to N-glycosylation defectDaniel Medina-Cano, Ekin Ucuncu, Lam Son Nguyen, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2025
MODELING TISSUE-RESIDENT MACROPHAGE DEVELOPMENT FROM MOUSE PLURIPOTENT STEM CELLSAnn K Baako, Ragavi Vijayakumar, Daniel Medina-Cano, et al.
Orphanet Journal of Rare Diseases|May 6, 2016
Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred populationHisham Megahed, Michaël Nicouleau, Giulia Barcia, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2024
A PLURIPOTENT STEM CELL PLATFORM FOR IN VITRO SYSTEMS GENETICS STUDIES OF MOUSE DEVELOPMENTRachel A Glenn, Stephanie C Do, Karthik Guruvayurappan, et al.
Brain : a Journal of Neurology|June 8, 2018
De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel geneJean Chemin, Karine Siquier-Pernet, Michaël Nicouleau, et al.
Nature Communications|December 1, 2020
MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar HypoplasiaEkin Ucuncu, Karthyayani Rajamani, Miranda S C Wilson, et al.
Brain : a Journal of Neurology|October 4, 2017
WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cellsMara Cavallin, Maria A Rujano, Nathalie Bednarek, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Development (Cambridge, England)|July 28, 2022
Rapid and robust directed differentiation of mouse epiblast stem cells into definitive endoderm and forebrain organoidsDaniel Medina-Cano, Emily K Corrigan, Rachel A Glenn, et al.
Developmental Cell|August 28, 2025
A mouse organoid platform for modeling cerebral cortex development and cis-regulatory evolution in vitroDaniel Medina-Cano, Mohammed T Islam, Veronika Petrova, et al.
Developmental Cell|August 20, 2025
Enhancer remodeling by OTX2 directs specification and patterning of mammalian definitive endodermLy-Sha Ee, Daniel Medina-Cano, Emily Goetzler, et al.
Elife|October 13, 2018
High N-glycan multiplicity is critical for neuronal adhesion and sensitizes the developing cerebellum to N-glycosylation defectDaniel Medina-Cano, Ekin Ucuncu, Lam Son Nguyen, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2025
MODELING TISSUE-RESIDENT MACROPHAGE DEVELOPMENT FROM MOUSE PLURIPOTENT STEM CELLSAnn K Baako, Ragavi Vijayakumar, Daniel Medina-Cano, et al.
Orphanet Journal of Rare Diseases|May 6, 2016
Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred populationHisham Megahed, Michaël Nicouleau, Giulia Barcia, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2024
A PLURIPOTENT STEM CELL PLATFORM FOR IN VITRO SYSTEMS GENETICS STUDIES OF MOUSE DEVELOPMENTRachel A Glenn, Stephanie C Do, Karthik Guruvayurappan, et al.
Brain : a Journal of Neurology|June 8, 2018
De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel geneJean Chemin, Karine Siquier-Pernet, Michaël Nicouleau, et al.
Nature Communications|December 1, 2020
MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar HypoplasiaEkin Ucuncu, Karthyayani Rajamani, Miranda S C Wilson, et al.
Brain : a Journal of Neurology|October 4, 2017
WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cellsMara Cavallin, Maria A Rujano, Nathalie Bednarek, et al.
Pageof 1