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 (31-40 of 59) with videos related to

Pageof 6
Sort By:
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|December 8, 2020
Whole-exome sequencing reveals novel vacuolar ATPase genes' variants and variants in genes involved in lysosomal biology and autophagosomal formation in oral granular cell tumorsJosiane Alves França, Tenzin Gayden, Eric Bareke, et al.
Disease Models & Mechanisms|May 20, 2022
Snrpb is required in murine neural crest cells for proper splicing and craniofacial morphogenesisSabrina Shameen Alam, Shruti Kumar, Marie-Claude Beauchamp, et al.
Journal of Sleep Research|December 16, 2021
Does the adenosine deaminase (ADA) gene confer risk of sleepwalking?Simon Fournier, Yves Dauvilliers, Simon C Warby, et al.
Cell Reports|November 18, 2020
H3K27M in Gliomas Causes a One-Step Decrease in H3K27 Methylation and Reduced Spreading within the Constraints of H3K36 MethylationAshot S Harutyunyan, Haifen Chen, Tianyuan Lu, et al.
Kidney International|January 8, 2019
Recessive mutation in CD2AP causes focal segmental glomerulosclerosis in humans and miceTomoko Takano, Eric Bareke, Naoki Takeda, et al.
Genome Research|April 9, 2022
H3K36 dimethylation shapes the epigenetic interaction landscape by directing repressive chromatin modifications in embryonic stem cellsHaifen Chen, Bo Hu, Cynthia Horth, et al.
Human Molecular Genetics|February 18, 2021
Mutation in Eftud2 causes craniofacial defects in mice via mis-splicing of Mdm2 and increased P53Marie-Claude Beauchamp, Anissa Djedid, Eric Bareke, et al.
American Journal of Medical Genetics. Part A|October 20, 2015
Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACEJulie Richer, Hussein Daoud, Pavel Geier, et al.
Molecular Genetics and Metabolism|March 20, 2025
Using multiple modalities to confirm diagnosis in patients with suspected peroxisome biogenesis disordersAnthony C T Cheung, Erminia Di Pietro, Catherine Argyriou, et al.
Reproductive Biomedicine Online|April 3, 2026
Lessons learned from the exome sequencing of nine cases of infertility and the way forwardJalal V Broojeni, Mohamed Elmahdy, Sacha Mitchell, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|December 8, 2020
Whole-exome sequencing reveals novel vacuolar ATPase genes' variants and variants in genes involved in lysosomal biology and autophagosomal formation in oral granular cell tumorsJosiane Alves França, Tenzin Gayden, Eric Bareke, et al.
Disease Models & Mechanisms|May 20, 2022
Snrpb is required in murine neural crest cells for proper splicing and craniofacial morphogenesisSabrina Shameen Alam, Shruti Kumar, Marie-Claude Beauchamp, et al.
Journal of Sleep Research|December 16, 2021
Does the adenosine deaminase (ADA) gene confer risk of sleepwalking?Simon Fournier, Yves Dauvilliers, Simon C Warby, et al.
Cell Reports|November 18, 2020
H3K27M in Gliomas Causes a One-Step Decrease in H3K27 Methylation and Reduced Spreading within the Constraints of H3K36 MethylationAshot S Harutyunyan, Haifen Chen, Tianyuan Lu, et al.
Kidney International|January 8, 2019
Recessive mutation in CD2AP causes focal segmental glomerulosclerosis in humans and miceTomoko Takano, Eric Bareke, Naoki Takeda, et al.
Genome Research|April 9, 2022
H3K36 dimethylation shapes the epigenetic interaction landscape by directing repressive chromatin modifications in embryonic stem cellsHaifen Chen, Bo Hu, Cynthia Horth, et al.
Human Molecular Genetics|February 18, 2021
Mutation in Eftud2 causes craniofacial defects in mice via mis-splicing of Mdm2 and increased P53Marie-Claude Beauchamp, Anissa Djedid, Eric Bareke, et al.
American Journal of Medical Genetics. Part A|October 20, 2015
Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACEJulie Richer, Hussein Daoud, Pavel Geier, et al.
Molecular Genetics and Metabolism|March 20, 2025
Using multiple modalities to confirm diagnosis in patients with suspected peroxisome biogenesis disordersAnthony C T Cheung, Erminia Di Pietro, Catherine Argyriou, et al.
Reproductive Biomedicine Online|April 3, 2026
Lessons learned from the exome sequencing of nine cases of infertility and the way forwardJalal V Broojeni, Mohamed Elmahdy, Sacha Mitchell, et al.
Pageof 6