Associate Professor
Huffington Center On Aging
Baylor College of Medicine
Houston, TX, US
Associate Professor
Molecular and Cellular Biology
Baylor College of Medicine
Associate Professor
Otolaryngology–Head and Neck Surgery
Baylor College of Medicine
Dan L Duncan Comprehensive Cancer Center
Baylor College of Medicine
Houston, Texas, United States
Graduate School of Biomedical Sciences
Initiative for Maximizing Student Development (IMSD) and Post-baccalaureate Research Education Program (PREP)


Advanced Training from Baylor College Of Medicine
Ph.D. from University Of Manitoba
B.Sc. from University Of Manitoba

Professional Interests

  • Signaling pathways in auditory development, aging and cancer prevention
  • Circadian Rhythms
  • Hearing and Balance disorders
  • Auditory neuropathy
  • Orphan Nuclear Receptors
  • Tinnitus
  • Lipidemia

Professional Statement

Our long-term goal is to enhance, protect, repair or regenerate hair cells, supporting cells and associated nerves in the mammalian hearing organ and neurons in the auditory cortex that are loss with age (development or aging) or due to noise, trauma and chemotherapeutic insults. We aim to identify molecules and their signaling pathways that modulate inner ear and brain cell function.

Deafness is a relatively common disorder, with approximately 1 in 1000 children born with a serious permanent hearing impairment, single gene defects account for over half of the cases of childhood deafness. The World Health Organization (WHO) estimated hearing loss and deafness affected at least 250 million people worldwide in 2002 and is an increasing challenge to public health as lifespan increases and the general population ages.

We have identified gene-signaling pathways important for development, aging and regeneration of hair cells and auditory neurons. We discovered that loss of the orphan nuclear receptor NR2F1 results in the production of extra hair cells and supporting cells (a stem cell pool) and changes in cortical neurogenesis. We are characterizing the signaling pathways NR2F1 regulates by performing biochemical, molecular, bioinformatic and computational, and transcriptome (chromatin boundaries and structure, epigenetic and transcriptional regulation of gene expression) analyses. One pathway involves circadian rhythms; a diurnal (24h) molecular clock that controls the synchronization of gene functions in response to environmental and cellular cues. We are characterizing how circadian rhythms regulate the development, aging and regeneration of hair cells and neurons at the molecular and organ level. Findings from these studies will help us to develop therapies to regenerate and/or protect aging hair cells and neurons.

We also investigate the structure and function of a novel membrane motor protein, SLC26A5 prestin (quick tempo protein) in outer hair cells (OHC). Prestin is responsible for the active feedback mechanism required for amplifying and selecting high frequency hearing, which is preferentially reduced with age. We discovered that prestin is localized in membrane microdomains or rafts and that changes in membrane cholesterol disrupts OHC functions. Indeed, humans that are dyslipidemic have reduced hearing abilities and we found that cholesterol is able to modulate and tune prestin activity and the hair cell motor for hearing. Studies are directed to understanding the mechanisms of prestin and OHC function with increasing age and in altered cholesterol environments.

Our studies hope to provide insights into understanding human disorders of auditory and neuronal function and to develop pharmacologic, gene or cell-based therapy to improve the quality of life during aging and cancer.

Selected Publications