Neil J Ingham

7PUBLICATIONS
26CO-AUTHORS
Neurology and neuromuscular diseasesMedical devicesGene expression (incl. microarray and other genome-wide approaches)Cell and nuclear divisionLinguistic structures (incl. phonology, morphology and syntax)
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Publications (7)

|Nov 25, 2024
Rescue of cochlear vascular pathology prevents sensory hair cell loss in Norrie disease.

Aara Patel, Valda Pauzuolyte, Neil J Ingham

|Aug 29, 2023
Systemic gene therapy rescues retinal dysfunction and hearing loss in a model of Norrie disease.

Valda Pauzuolyte, Aara Patel, James R Wawrzynski

|Aug 08, 2023
Reversal of an existing hearing loss by gene activation in Spns2 mutant mice.

Elisa Martelletti, Neil J Ingham, Karen P Steel

|May 11, 2023
Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variants.

María Lachgar-Ruiz, Matías Morín, Elisa Martelletti

|Jun 21, 2022
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.

Guney Bademci, María Lachgar-Ruiz, Mangesh Deokar

|Oct 01, 2021
Inner hair cell dysfunction in Klhl18 mutant mice leads to low frequency progressive hearing loss.

Neil J Ingham, Navid Banafshe, Clarisse Panganiban

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Frequent Collaborators

5 joint publications

Karen P Steel

2 joint publications

Morag A Lewis

2 joint publications

Elisa Martelletti

2 joint publications

Valda Pauzuolyte