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Iftekhar A Showpnil

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Genes & Cancer|March 23, 2019
Transcriptomic analysis functionally maps the intrinsically disordered domain of EWS/FLI and reveals novel transcriptional dependencies for oncogenesisEmily R Theisen, Kyle R Miller, Iftekhar A Showpnil, et al.
Journal of Visualized Experiments : Jove|July 14, 2020
Mapping the Structure-Function Relationships of Disordered Oncogenic Transcription Factors Using Transcriptomic AnalysisIftekhar A Showpnil, Kyle R Miller, Cenny Taslim, et al.
Biorxiv : the Preprint Server for Biology|February 14, 2024
DBD-α4 helix of EWSR1::FLI1 is required for GGAA microsatellite binding that underlies genome regulation in Ewing sarcomaAriunaa Bayanjargal, Cenny Taslim, Iftekhar A Showpnil, et al.
Nucleic Acids Research|September 20, 2022
EWS/FLI mediated reprogramming of 3D chromatin promotes an altered transcriptional state in Ewing sarcomaIftekhar A Showpnil, Julia Selich-Anderson, Cenny Taslim, et al.
Elife|June 15, 2026
The DBD-α4 helix of EWSR1::FLI1 is required for GGAA microsatellite binding that underlies genome regulation in Ewing sarcomaAriunaa Bayanjargal, Cenny Taslim, Iftekhar A Showpnil, et al.
American Journal of Medical Genetics. Part A|October 11, 2025
De Novo Heterozygous ZFX Frameshift Variant in a Female With an X-Linked Neurodevelopmental DisorderIftekhar A Showpnil, Allison Daley, Emily R Sites, et al.
Clinical Genetics|November 7, 2025
Detection of the Heterozygous Recurrent MAX p.(Arg60Gln) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly-Macrocephaly SyndromeIftekhar A Showpnil, Neta Feinstein-Goren, Lior Greenbaum, et al.
Oncogene|June 19, 2021
The FLI portion of EWS/FLI contributes a transcriptional regulatory function that is distinct and separable from its DNA-binding function in Ewing sarcomaMegann A Boone, Cenny Taslim, Jesse C Crow, et al.
HGG Advances|November 5, 2024
Expanding the phenotypic spectrum of CSNK2A1-associated Okur-Chung neurodevelopmental syndromeSwetha Ramadesikan, Iftekhar A Showpnil, Mohammad Marhabaie, et al.
NPJ Genomic Medicine|December 18, 2024
Long-read genome sequencing resolves complex genomic rearrangements in rare genetic syndromesIftekhar A Showpnil, Maria E Hernandez Gonzalez, Swetha Ramadesikan, et al.
Pageof 1

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

Sort By:
Pageof 1
Genes & Cancer|March 23, 2019
Transcriptomic analysis functionally maps the intrinsically disordered domain of EWS/FLI and reveals novel transcriptional dependencies for oncogenesisEmily R Theisen, Kyle R Miller, Iftekhar A Showpnil, et al.
Journal of Visualized Experiments : Jove|July 14, 2020
Mapping the Structure-Function Relationships of Disordered Oncogenic Transcription Factors Using Transcriptomic AnalysisIftekhar A Showpnil, Kyle R Miller, Cenny Taslim, et al.
Biorxiv : the Preprint Server for Biology|February 14, 2024
DBD-α4 helix of EWSR1::FLI1 is required for GGAA microsatellite binding that underlies genome regulation in Ewing sarcomaAriunaa Bayanjargal, Cenny Taslim, Iftekhar A Showpnil, et al.
Nucleic Acids Research|September 20, 2022
EWS/FLI mediated reprogramming of 3D chromatin promotes an altered transcriptional state in Ewing sarcomaIftekhar A Showpnil, Julia Selich-Anderson, Cenny Taslim, et al.
Elife|June 15, 2026
The DBD-α4 helix of EWSR1::FLI1 is required for GGAA microsatellite binding that underlies genome regulation in Ewing sarcomaAriunaa Bayanjargal, Cenny Taslim, Iftekhar A Showpnil, et al.
American Journal of Medical Genetics. Part A|October 11, 2025
De Novo Heterozygous ZFX Frameshift Variant in a Female With an X-Linked Neurodevelopmental DisorderIftekhar A Showpnil, Allison Daley, Emily R Sites, et al.
Clinical Genetics|November 7, 2025
Detection of the Heterozygous Recurrent MAX p.(Arg60Gln) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly-Macrocephaly SyndromeIftekhar A Showpnil, Neta Feinstein-Goren, Lior Greenbaum, et al.
Oncogene|June 19, 2021
The FLI portion of EWS/FLI contributes a transcriptional regulatory function that is distinct and separable from its DNA-binding function in Ewing sarcomaMegann A Boone, Cenny Taslim, Jesse C Crow, et al.
HGG Advances|November 5, 2024
Expanding the phenotypic spectrum of CSNK2A1-associated Okur-Chung neurodevelopmental syndromeSwetha Ramadesikan, Iftekhar A Showpnil, Mohammad Marhabaie, et al.
NPJ Genomic Medicine|December 18, 2024
Long-read genome sequencing resolves complex genomic rearrangements in rare genetic syndromesIftekhar A Showpnil, Maria E Hernandez Gonzalez, Swetha Ramadesikan, et al.
Pageof 1