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Sydney Steiman

Showing results (1-10 of 7) with videos related to

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Molecular and Cellular Biology|March 14, 2024
FoxP1 Represses MEF2A in Striated MuscleSydney Steiman, Tetsuaki Miyake, John C McDermott
NPJ Genomic Medicine|May 6, 2026
Bridging the gap: an emerging link between tubulinopathies and ciliopathiesSydney Steiman, Safia Omer, Stephen Pastore, et al.
Molecular Therapy. Nucleic Acids|November 7, 2024
Multi-gene duplication removal in an engineered human cellular MECP2 duplication syndrome model with an <i>IRAK1-MECP2</i> duplicationSamar Z Rizvi, Wing Suen Chan, Eleonora Maino, et al.
Journal of Neuroinflammation|April 8, 2026
A novel humanized mouse model exhibits neurobehavioral impairments and recapitulates key neuropathological features of infantile Tay-Sachs diseaseLujaina Elbakr, Georgiana Forguson, Hong Anh Truong, et al.
Disease Models & Mechanisms|September 29, 2020
A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic <i>Dmd</i> deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathyTatianna Wai Ying Wong, Abdalla Ahmed, Grace Yang, et al.
Disease Models & Mechanisms|April 4, 2025
Correction: A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathyTatianna Wai, Ying Wong, Abdalla Ahmed, et al.
Nature Communications|November 27, 2025
Mutations in the β-tubulin TUBB impair ciliogenesis and are associated with ciliopathy-like phenotypesAntonio Mollica, Safia Omer, Georgiana Forguson, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Molecular and Cellular Biology|March 14, 2024
FoxP1 Represses MEF2A in Striated MuscleSydney Steiman, Tetsuaki Miyake, John C McDermott
NPJ Genomic Medicine|May 6, 2026
Bridging the gap: an emerging link between tubulinopathies and ciliopathiesSydney Steiman, Safia Omer, Stephen Pastore, et al.
Molecular Therapy. Nucleic Acids|November 7, 2024
Multi-gene duplication removal in an engineered human cellular MECP2 duplication syndrome model with an <i>IRAK1-MECP2</i> duplicationSamar Z Rizvi, Wing Suen Chan, Eleonora Maino, et al.
Journal of Neuroinflammation|April 8, 2026
A novel humanized mouse model exhibits neurobehavioral impairments and recapitulates key neuropathological features of infantile Tay-Sachs diseaseLujaina Elbakr, Georgiana Forguson, Hong Anh Truong, et al.
Disease Models & Mechanisms|September 29, 2020
A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic <i>Dmd</i> deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathyTatianna Wai Ying Wong, Abdalla Ahmed, Grace Yang, et al.
Disease Models & Mechanisms|April 4, 2025
Correction: A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathyTatianna Wai, Ying Wong, Abdalla Ahmed, et al.
Nature Communications|November 27, 2025
Mutations in the β-tubulin TUBB impair ciliogenesis and are associated with ciliopathy-like phenotypesAntonio Mollica, Safia Omer, Georgiana Forguson, et al.
Pageof 1