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 (21-30 of 59) with videos related to

Pageof 6
Sort By:
BMC Bioinformatics|October 15, 2010
Functional analysis: evaluation of response intensities--tailoring ANOVA for lists of expression subsetsFabrice Berger, Bertrand De Meulder, Anthoula Gaigneaux, et al.
Clinical Genetics|February 5, 2025
Two Novel Protein-Truncating Variants in NLRP2 and Their Functional Impacts on the Subcortical Maternal ComplexZeynep Yalcin, Zheng Gao, Ibrahim M Abdelrazek, et al.
Cell Reports|February 24, 2021
Chromatin dysregulation associated with NSD1 mutation in head and neck squamous cell carcinomaNargess Farhangdoost, Cynthia Horth, Bo Hu, et al.
Human Molecular Genetics|September 22, 2017
SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase Cɛ) impairing TORC2-dependent AKT activationDiana Alcantara, Frances Elmslie, Martine Tetreault, et al.
Genome Biology|October 10, 2024
Systematic perturbations of SETD2, NSD1, NSD2, NSD3, and ASH1L reveal their distinct contributions to H3K36 methylationGerry A Shipman, Reinnier Padilla, Cynthia Horth, et al.
Journal of Assisted Reproduction and Genetics|January 26, 2024
A report of two homozygous TERB1 protein-truncating variants in two unrelated women with primary infertilityZeynep Yalcin, Manqi Liang, Ibrahim M Abdelrazek, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 18, 2024
Etiology of craniofacial and cardiac malformations in a mouse model of <i>SF3B4</i>-related syndromesShruti Kumar, Eric Bareke, Jimmy Lee, et al.
Biorxiv : the Preprint Server for Biology|October 31, 2023
Systematic perturbations of SETD2, NSD1, NSD2, NSD3 and ASH1L reveals their distinct contributions to H3K36 methylationGerry A Shipman, Reinnier Padilla, Cynthia Horth, et al.
NPJ Genomic Medicine|June 7, 2022
Novel homozygous nonsense mutation of MLIP and compensatory alternative splicingJean Mezreani, Sébastien Audet, Florence Martin, et al.
Pediatric Blood & Cancer|May 17, 2017
H3.1 K36M mutation in a congenital-onset soft tissue neoplasmKristin D Kernohan, David Grynspan, Raveena Ramphal, et al.
Pageof 6

Showing results (21-30 of 59) with videos related to

Sort By:
Pageof 6
BMC Bioinformatics|October 15, 2010
Functional analysis: evaluation of response intensities--tailoring ANOVA for lists of expression subsetsFabrice Berger, Bertrand De Meulder, Anthoula Gaigneaux, et al.
Clinical Genetics|February 5, 2025
Two Novel Protein-Truncating Variants in NLRP2 and Their Functional Impacts on the Subcortical Maternal ComplexZeynep Yalcin, Zheng Gao, Ibrahim M Abdelrazek, et al.
Cell Reports|February 24, 2021
Chromatin dysregulation associated with NSD1 mutation in head and neck squamous cell carcinomaNargess Farhangdoost, Cynthia Horth, Bo Hu, et al.
Human Molecular Genetics|September 22, 2017
SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase Cɛ) impairing TORC2-dependent AKT activationDiana Alcantara, Frances Elmslie, Martine Tetreault, et al.
Genome Biology|October 10, 2024
Systematic perturbations of SETD2, NSD1, NSD2, NSD3, and ASH1L reveal their distinct contributions to H3K36 methylationGerry A Shipman, Reinnier Padilla, Cynthia Horth, et al.
Journal of Assisted Reproduction and Genetics|January 26, 2024
A report of two homozygous TERB1 protein-truncating variants in two unrelated women with primary infertilityZeynep Yalcin, Manqi Liang, Ibrahim M Abdelrazek, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 18, 2024
Etiology of craniofacial and cardiac malformations in a mouse model of <i>SF3B4</i>-related syndromesShruti Kumar, Eric Bareke, Jimmy Lee, et al.
Biorxiv : the Preprint Server for Biology|October 31, 2023
Systematic perturbations of SETD2, NSD1, NSD2, NSD3 and ASH1L reveals their distinct contributions to H3K36 methylationGerry A Shipman, Reinnier Padilla, Cynthia Horth, et al.
NPJ Genomic Medicine|June 7, 2022
Novel homozygous nonsense mutation of MLIP and compensatory alternative splicingJean Mezreani, Sébastien Audet, Florence Martin, et al.
Pediatric Blood & Cancer|May 17, 2017
H3.1 K36M mutation in a congenital-onset soft tissue neoplasmKristin D Kernohan, David Grynspan, Raveena Ramphal, et al.
Pageof 6