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

Eric Bareke

Showing results (41-50 of 59) with videos related to

Pageof 6
Sort By:
American Journal of Medical Genetics. Part A|April 23, 2015
Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACEJulie Richer, Hussein Daoud, Pavel Geier, et al.
Brain : a Journal of Neurology|December 12, 2017
POLR3A variants in hereditary spastic paraplegia and ataxiaLaurence Gauquelin, Martine Tétreault, Isabelle Thiffault, et al.
Cancer Research Communications|April 13, 2026
ATR and PKMYT1 inhibition re-sensitize a subset of TNBC patient-derived models to carboplatin inducing mitotic catastropheJuliet Guay, Hellen Kuasne, Catherine Chabot, et al.
Scientific Reports|September 8, 2020
Prognostic and predictive value of circulating tumor DNA during neoadjuvant chemotherapy for triple negative breast cancerLuca Cavallone, Adriana Aguilar-Mahecha, Josiane Lafleur, et al.
Genes|January 23, 2024
The Mutational Spectrum of Pre- and Post-Neoadjuvant Chemotherapy Triple-Negative Breast CancersAdriana Aguilar-Mahecha, Najmeh Alirezaie, Josiane Lafleur, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|June 1, 2016
Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unitHussein Daoud, Stephanie M Luco, Rui Li, et al.
Molecular Medicine (Cambridge, Mass.)|March 21, 2025
Spatiotemporal diversity in molecular and functional abnormalities in the mdx dystrophic brainJoanna Pomeroy, Malgorzata Borczyk, Maria Kawalec, et al.
Brain : a Journal of Neurology|June 11, 2021
TDP-43 stabilizes G3BP1 mRNA: relevance to amyotrophic lateral sclerosis/frontotemporal dementiaHadjara Sidibé, Yousra Khalfallah, Shangxi Xiao, et al.
Brain : a Journal of Neurology|November 7, 2016
Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportionNasim Vasli, Elizabeth Harris, Jason Karamchandani, et al.
Nature Communications|November 3, 2018
TRPV4 and KRAS and FGFR1 gain-of-function mutations drive giant cell lesions of the jawCarolina Cavalieri Gomes, Tenzin Gayden, Andrea Bajic, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|April 23, 2015
Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACEJulie Richer, Hussein Daoud, Pavel Geier, et al.
Brain : a Journal of Neurology|December 12, 2017
POLR3A variants in hereditary spastic paraplegia and ataxiaLaurence Gauquelin, Martine Tétreault, Isabelle Thiffault, et al.
Cancer Research Communications|April 13, 2026
ATR and PKMYT1 inhibition re-sensitize a subset of TNBC patient-derived models to carboplatin inducing mitotic catastropheJuliet Guay, Hellen Kuasne, Catherine Chabot, et al.
Scientific Reports|September 8, 2020
Prognostic and predictive value of circulating tumor DNA during neoadjuvant chemotherapy for triple negative breast cancerLuca Cavallone, Adriana Aguilar-Mahecha, Josiane Lafleur, et al.
Genes|January 23, 2024
The Mutational Spectrum of Pre- and Post-Neoadjuvant Chemotherapy Triple-Negative Breast CancersAdriana Aguilar-Mahecha, Najmeh Alirezaie, Josiane Lafleur, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|June 1, 2016
Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unitHussein Daoud, Stephanie M Luco, Rui Li, et al.
Molecular Medicine (Cambridge, Mass.)|March 21, 2025
Spatiotemporal diversity in molecular and functional abnormalities in the mdx dystrophic brainJoanna Pomeroy, Malgorzata Borczyk, Maria Kawalec, et al.
Brain : a Journal of Neurology|June 11, 2021
TDP-43 stabilizes G3BP1 mRNA: relevance to amyotrophic lateral sclerosis/frontotemporal dementiaHadjara Sidibé, Yousra Khalfallah, Shangxi Xiao, et al.
Brain : a Journal of Neurology|November 7, 2016
Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportionNasim Vasli, Elizabeth Harris, Jason Karamchandani, et al.
Nature Communications|November 3, 2018
TRPV4 and KRAS and FGFR1 gain-of-function mutations drive giant cell lesions of the jawCarolina Cavalieri Gomes, Tenzin Gayden, Andrea Bajic, et al.
Pageof 6