University research records

Centre of Excellence in Molecular Biology

7 imported, source-linked research records. All imported publication dates.

All imported publication dates

7 matching research records

Topic: Hearing ageing. Only records linked to Centre of Excellence in Molecular Biology are included. Historical ingestion is still running; these are imported records, not a count of all research worldwide.

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Showing 1–7 of 7 matching records. Counts update as records arrive.

  1. Author Correction: Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48

    August 26, 2025 · 2 citations · Open access

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  2. Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness

    September 24, 2020 · 20 citations · Open access

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  3. Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse

    March 28, 2018 · 48 citations · Open access

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  4. Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p

    June 9, 2011 · 58 citations · Open access

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  5. Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74

    December 24, 2010 · 122 citations · Open access

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  6. In Silico Study of Human Gap Junction Beta-2 Protein by Homology Modeling

    June 30, 2010 · 0 citations · Open access

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  7. DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2‐q15

    July 24, 2009 · 16 citations

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