Author

Inna A. Belyantseva

National Institutes of HealthORCID 0000-0001-5030-9784Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Cell Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:human· 2 Organism:mouse· 2 Approach:statistical model· 2 Research Focus:cell signaling & trafficking· 1 Assay:fluorescence / live-cell microscopy· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Thomas B. FriedmaniD· 4 shared Emma M. JenkinsoniD· 2 shared Jill E. UrquhartiD· 2 shared Kevin James MunroiD· 2 shared Kyle Thompson· 2 shared Leigh A. M. DemainiD· 2 shared Melanie BarzikiD· 2 shared Raymond T. O’KeefeiD· 2 shared

Activity by Year

2017-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersGenetics

Thomas B. FriedmanORCID

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4 papers

Recent·Most cited

Cell BiologyNature CommunicationsPeer-reviewedSep 1, 2025

Live-cell single-molecule fluorescence microscopy for protruding organelles reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of inner ear hair cells

Takushi Miyoshi, Harshad D. Vishwasrao, Inna A. Belyantseva…·Thomas B. Friedman

This study uses live-cell single-molecule fluorescence microscopy to investigate MYO7A trafficking in stereocilia, revealing its dimeric form and movement restrictions mediated by plasma membrane and F-actin interactions.

1 citation

mousefluorescence / live-cell microscopy

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GeneticsbioRxivPreprintMar 4, 2025

Methionine sulfoxide reductase B3 antioxidant activity is indispensable for mouse inner ear cuticular plate structure and hair bundle integrity

Gowri Nayak, Élodie M. Richard, Byung Cheon Lee…·Saima Riazuddin

This study shows that MSRB3 is essential for maintaining inner ear structure and hair bundle integrity in mice, with its antioxidant activity protecting actin redox dynamics.

DOI 10.1101/2025.03.04.641487

mouseexperimental assay

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Genetic & Genomic MedicinemedRxivPreprintAug 19, 2024

Biallelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered intrinsic and extrinsic apoptosis and a Perrault syndrome-spectrum phenotype

Thomas B. Smith, Robert Kopajtich, Leigh A. M. Demain…·William G. Newman

This study identifies biallelic DAP3 variants causing mitoribosomal dysfunction, leading to combined oxidative phosphorylation deficiency and Perrault syndrome-like features.

2 citations

humanproteomics

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GeneticsbioRxivPreprintJul 25, 2017

A homozygous variant in mitochondrial RNase P subunit PRORP is associated with Perrault syndrome characterized by hearing loss and primary ovarian insufficiency

Irit Hochberg, Leigh A. M. Demain, Jill E. Urquhart…·William G. Newman

The paper identifies a homozygous variant in KIAA0391 (PRORP) as a cause of Perrault syndrome, showing reduced mitochondrial RNase P activity and impaired tRNA processing.

7 citations

humanstatistical model

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