Kumar Alagramam

A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15.

Assessment of retinal structure and function in Ames waltzer mice.

Interactions in the network of Usher syndrome type 1 proteins.

Characterization of a new allele of Ames waltzer generated by ENU mutagenesis.

Characterization of vestibular dysfunction in the mouse model for Usher syndrome 1F.

The basic science of Meniere's disease and endolymphatic hydrops.

A quantitative survey of gravity receptor function in mutant mouse strains.

Progression of inner ear pathology in Ames waltzer mice and the role of protocadherin 15 in hair cell development.

Gene expression analysis of distinct populations of cells isolated from mouse and human inner ear FFPE tissue using laser capture microdissection--a technical report based on preliminary findings.

Inner ear proteomics of mouse models for deafness, a discovery strategy.

N-Acetyl L-cysteine does not protect against premature age-related hearing loss in C57BL/6J mice: a pilot study.

Optimization of ribonucleic acid detection from archival Guinea pig temporal bone specimens.

Identification and characterization of mouse cochlear stem cells.

Molecular changes associated with the endolymphatic hydrops model.

Tympanometry assessment of 61 inbred strains of mice.

Promoter, alternative splice forms, and genomic structure of protocadherin 15.

Development of outer hair cells in Ames waltzer mice: mutation in protocadherin 15 affects development of cuticular plate and associated structures.

A mouse model with postnatal endolymphatic hydrops and hearing loss.

Spiral ganglion degeneration patterns in endolymphatic hydrops.

Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation.

Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton.

Foreword for special issue: mouse models for hearing research.

A nonsynonymous SNP within PCDH15 is associated with lipid traits in familial combined hyperlipidemia.

Spiral ganglion loss outpaces inner hair cell loss in endolymphatic hydrops.

Photodynamic therapy of cottontail rabbit papillomavirus-induced papillomas in a severe combined immunodeficient mouse xenograft system.

Proteomics, bioinformatics and targeted gene expression analysis reveals up-regulation of cochlin and identifies other potential biomarkers in the mouse model for deafness in Usher syndrome type 1F.

N-Acetyl L-Cysteine does not protect mouse ears from the effects of noise*.

Pharmacological protection of hearing loss in the mouse model of endolymphatic hydrops.

Mutations in protocadherin 15 and cadherin 23 affect tip links and mechanotransduction in mammalian sensory hair cells.