Michael R. Bowl

London, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 44 publications

Compensatory Interplay Between Clarin-1 and Clarin-2 Deafness-Associated Proteins Governs Phenotypic Variability in Hearing.

Compensatory Interplay Between Clarin-1 and Clarin-2 Deafness-Associated Proteins Governs Phenotypic Variability in Hearing.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: October 30, 2025

TMEM145 is a principal component of outer hair cell stereocilia.

TMEM145 is a principal component of outer hair cell stereocilia.

Journal: Neuron
Published: May 27, 2025

International Consortium on Ageing-Related Pathologies (ICCARP) Audiovestibular Group: fostering international consensus to refine International Classification of Diseases (ICD-11) codes for hearing loss across the life course.

International Consortium on Ageing-Related Pathologies (ICCARP) Audiovestibular Group: fostering international consensus to refine International Classification of Diseases (ICD-11) codes for hearing loss across the life course.

Journal: GeroScience
Published: May 02, 2025

C57BL/6-derived mice and the Cdh23ahl allele - Background matters.

C57BL/6-derived mice and the Cdh23ahl allele - Background matters.

Journal: Hearing research
Published: January 14, 2025

Cross-species validation of a human age-related hearing loss candidate KLHDC7B as essential for mammalian hearing.

Cross-species validation of a human age-related hearing loss candidate KLHDC7B as essential for mammalian hearing.

Journal: Communications biology
Published: January 09, 2025

CIB2 function is distinct from Whirlin in the development of cochlear stereocilia staircase pattern.

CIB2 function is distinct from Whirlin in the development of cochlear stereocilia staircase pattern.

Journal: bioRxiv : the preprint server for biology
Published: August 12, 2024

CIB2 function is distinct from that of whirlin in the organization of sterocilia architecture.

CIB2 function is distinct from that of whirlin in the organization of sterocilia architecture.

Journal: Disease models & mechanisms
Published: July 30, 2024

Expanding the spectrum of phenotypes for MPDZ: Report of four unrelated families and review of the literature.

Expanding the spectrum of phenotypes for MPDZ: Report of four unrelated families and review of the literature.

Journal: Clinical genetics
Published: February 22, 2024

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data.

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data.

Journal: medRxiv : the preprint server for health sciences
Published: January 10, 2024

Rare disease gene association discovery in the 100,000 Genomes Project.

Rare disease gene association discovery in the 100,000 Genomes Project.

Journal: Nature
Published: December 19, 2023

Clarin-2 gene supplementation durably preserves hearing in a model of progressive hearing loss.

Clarin-2 gene supplementation durably preserves hearing in a model of progressive hearing loss.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: October 20, 2023

BAI1 localizes AMPA receptors at the cochlear afferent post-synaptic density and is essential for hearing.

BAI1 localizes AMPA receptors at the cochlear afferent post-synaptic density and is essential for hearing.

Journal: Cell reports
Published: September 14, 2023
Showing 1-12 of 44

Last Updated: 09/26/2026