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Neuroscience

D-Index
47
Citations
9601
World Ranking
6385
National Ranking
2780

Overview

Inna A. Belyantseva is affiliated with the National Institutes of Health in the United States. Their research spans multiple fields primarily within Biochemistry, Genetics and Molecular Biology as well as Neuroscience. Subfields of particular focus include Molecular Biology, Sensory Systems, Cell Biology, Neurology, and Biomedical Engineering.

Their work addresses a range of main topics such as Hearing, Cochlea, Tinnitus, Genetics, Vestibular and auditory disorders, Cellular transport and secretion, Mitochondrial Function and Pathology, Ear Surgery and Otitis Media, Hearing Loss and Rehabilitation, and RNA and protein synthesis mechanisms.

Recent publications by this researcher include:

  • Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations, 2021, The American Journal of Human Genetics
  • Myosins and Hearing, 2020, Advances in experimental medicine and biology
  • Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin, 2021, Current Biology
  • Semi-automated single-molecule microscopy screening of fast-dissociating specific antibodies directly from hybridoma cultures, 2021, Cell Reports
  • Dual-AAV vector-mediated expression of MYO7A improves vestibular function in a mouse model of Usher syndrome 1B, 2023, Molecular Therapy - Methods & Clinical Development

Belyantseva frequently collaborates with several researchers, including Thomas B. Friedman, Risa Tona, Takushi Miyoshi, Rizwan Yousaf, and Yasuko Ishibashi.

Their publications commonly appear in venues such as bioRxiv (Cold Spring Harbor Laboratory), The American Journal of Human Genetics, The Journal of Cell Biology, Molecular Therapy, and Journal of Biological Chemistry.

Best Publications

  • Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

    Edward R Wilcox;Quianna L Burton;Sadaf Naz;Saima Riazuddin;Saima Riazuddin

  • Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.

    Federica Di Palma;Ralph H. Holme;Elizabeth C. Bryda;Inna A. Belyantseva

  • Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome

    Lorraine A. Everett;Inna A. Belyantseva;Konrad Noben-Trauth;Raquel Cantos

  • Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration

    Tamar Ben-Yosef;Inna A. Belyantseva;Thomas L. Saunders;Elizabeth D. Hughes

  • Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia.

    Inna A. Belyantseva;Erich T. Boger;Erich T. Boger;Sadaf Naz;Gregory I. Frolenkov

  • Tricellulin Is a Tight-Junction Protein Necessary for Hearing

    Saima Riazuddin;Saima Riazuddin;Zubair M. Ahmed;Alan S. Fanning;Ayala Lagziel

  • PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

    Zubair M. Ahmed;Saima Riazuddin;Jamil Ahmad;Steve L. Bernstein

  • Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle.

    Inna A. Belyantseva;Erich T. Boger;Thomas B. Friedman

  • The Tip-Link Antigen, a Protein Associated with the Transduction Complex of Sensory Hair Cells, Is Protocadherin-15

    Zubair M. Ahmed;Richard Goodyear;Saima Riazuddin;Ayala Lagziel

  • Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48

    Saima Riazuddin;Inna A Belyantseva;Arnaud P J Giese;Kwanghyuk Lee

  • Genetic insights into the morphogenesis of inner ear hair cells

    Gregory I Frolenkov;Inna A Belyantseva;Thomas B Friedman;Andrew J Griffith

  • Expression and localization of prestin and the sugar transporter GLUT-5 during development of electromotility in cochlear outer hair cells.

    Inna A. Belyantseva;Henry J. Adler;Rui Curi;Gregory I. Frolenkov

  • Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice.

    Federica Di Palma;Inna A. Belyantseva;Hung J. Kim;Thomas F. Vogt

  • Rapid renewal of auditory hair bundles.

    Mark E. Schneider;Inna A. Belyantseva;Ricardo B. Azevedo;Bechara Kachar

  • Deafness and stria vascularis defects in S1P2 receptor-null mice.

    Mari Kono;Inna A. Belyantseva;Athanasia Skoura;Gregory I. Frolenkov

  • Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79

    Atteeq Ur Rehman;Atteeq Ur Rehman;Robert J. Morell;Inna A. Belyantseva;Shahid Y. Khan

  • Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2.

    Yong Liang;Yong Liang;Aihui Wang;Aihui Wang;Inna A. Belyantseva;David W. Anderson

  • Actin-Bundling Protein TRIOBP Forms Resilient Rootlets of Hair Cell Stereocilia Essential for Hearing

    Shin Ichiro Kitajiri;Takeshi Sakamoto;Inna A. Belyantseva;Richard J. Goodyear

  • γ-Actin is required for cytoskeletal maintenance but not development

    Inna A. Belyantseva;Benjamin J. Perrin;Kevin J. Sonnemann;Mei Zhu

  • Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome

    Kevin Isgrig;Jack W. Shteamer;Inna A. Belyantseva;Meghan C. Drummond

  • Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development.

    Ayala Lagziel;Zubair M. Ahmed;Julie M. Schultz;Robert J. Morell

Frequent Co-Authors

Thomas B. Friedman
Thomas B. Friedman National Institutes of Health
Zubair M. Ahmed
Zubair M. Ahmed University of Maryland, Baltimore
Saima Riazuddin
Saima Riazuddin University of Maryland, Baltimore
Sheikh Riazuddin
Sheikh Riazuddin University of Health Sciences Lahore
Robert J. Morell
Robert J. Morell National Institutes of Health
Andrew J. Griffith
Andrew J. Griffith National Institutes of Health
Sally A. Camper
Sally A. Camper University of Michigan–Ann Arbor
Sherri M. Jones
Sherri M. Jones University of Nebraska–Lincoln
Andrew Forge
Andrew Forge University College London
Suzanne M. Leal
Suzanne M. Leal Columbia University Medical Center

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