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Christina L Magyar

Showing results (1-10 of 5) with videos related to

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Organic & Biomolecular Chemistry|August 14, 2019
Triflic anhydride mediated synthesis of 3,4-dihydroquinazolines: a three-component one-pot tandem procedureChristina L Magyar, Tyler J Wall, Steven B Davies, et al.
Bioorganic & Medicinal Chemistry Letters|January 29, 2021
Dihydroquinazolines enhance 20S proteasome activity and induce degradation of α-synuclein, an intrinsically disordered protein associated with neurodegenerationTaylor J Fiolek, Christina L Magyar, Tyler J Wall, et al.
American Journal of Medical Genetics. Part A|February 23, 2022
PRUNE1 c.933G>A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literatureChristina L Magyar, David R Murdock, Lindsay C Burrage, et al.
Annals of Neurology|March 27, 2022
An Integrated Phenotypic and Genotypic Approach Reveals a High-Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger DomainCole A Deisseroth, Vanesa C Lerma, Christina L Magyar, et al.
HGG Advances|June 11, 2025
The Impact of Genetic Ancestry on Survival Outcomes in Pediatric Rhabdomyosarcoma: A Report from the Children's Oncology GroupEkene A Onwuka, Christina L Magyar, Bailey A Martin-Giacalone, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Organic & Biomolecular Chemistry|August 14, 2019
Triflic anhydride mediated synthesis of 3,4-dihydroquinazolines: a three-component one-pot tandem procedureChristina L Magyar, Tyler J Wall, Steven B Davies, et al.
Bioorganic & Medicinal Chemistry Letters|January 29, 2021
Dihydroquinazolines enhance 20S proteasome activity and induce degradation of α-synuclein, an intrinsically disordered protein associated with neurodegenerationTaylor J Fiolek, Christina L Magyar, Tyler J Wall, et al.
American Journal of Medical Genetics. Part A|February 23, 2022
PRUNE1 c.933G>A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literatureChristina L Magyar, David R Murdock, Lindsay C Burrage, et al.
Annals of Neurology|March 27, 2022
An Integrated Phenotypic and Genotypic Approach Reveals a High-Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger DomainCole A Deisseroth, Vanesa C Lerma, Christina L Magyar, et al.
HGG Advances|June 11, 2025
The Impact of Genetic Ancestry on Survival Outcomes in Pediatric Rhabdomyosarcoma: A Report from the Children's Oncology GroupEkene A Onwuka, Christina L Magyar, Bailey A Martin-Giacalone, et al.
Pageof 1