Anterior Segment Disorders and Dry Eye
The Cheng Lab
The Cheng Lab aims to understand the mechanisms for establishing and maintaining lifelong homeostasis and transparency in the eye lens. While decades of studies have identified the genes required to make a transparent lens, there remain many unanswered questions about basic lens cell biology that hinder the development of pharmaceuticals to prevent or delay age-related lens pathologies, including cataracts and presbyopia. 
In humans, ciliary muscles contract to change the tension of zonule fibers to deform the lens, increasing the len's optical power to focus on nearby objects, a process known as accommodation. This image shows a 3D reconstruction of a confocal z-stack through a human lens with attached cilliary body and zonules. The zonules are stained with wheat germ agglutinin (cell membrane marker, red) and microfibril-associated glycoprotein MAGP-1 (zonules, yellow). The ciliary body (in the foreground of the image) and the lens (behind the zonules) are stained for filamentous actin (F-actin, phalloidin, green) and cell nuclei (DAPI, blue)
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The Shyam Lab
The Shyam Lab works on identifying the mechanisms that regulate homeostasis in various ocular regions. We currently use biochemistry, molecular biology and microscopy techniques to identify the role of protein clearance pathways in the health of corneal endothelium. 
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Frontiers of Optical Imaging and Biology Lab
Patrice Tankam, Ph.D.
Optical imaging techniques such as optical coherence tomography (OCT) and fluorescence microscopy (FM) have enabled tremendous discoveries in biological and clinical research. However, the need for enhancing technological innovations to enable a better understanding of cellular processes involved in developmental and pathological conditions is still manifest. Dr. Tankam's lab uses a translational research approach that spans from the mechanistic understanding of corneal diseases using transgenic mice to disease diagnosis and management in humans. The group focuses on developing advanced imaging systems, including an integrated cellular-resolution OCT and FM to track the dynamics of cellular processes in vivo in the same transgenic mouse over time, as well as cellular-resolution OCT systems for human corneal imaging. The group is particularly interested in understanding the structural and physiological remodeling of the cornea and the iridocorneal angle in pathological conditions such as myopia, Fuchs endothelial corneal dystrophy, and primary open angle glaucoma.
Corneal Imaging with Cellular-resolution Optical Coherence Tomography
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Dr. Anna Tichenor
Dr. Anna Tichenor’s translational clinical research is focused primarily on understanding mucins on the ocular surface and examining the effects of dry eye inflammation on these mucins. Dr. Tichenor’s other research interests include exploring tear film flow, break up dynamics, composition, and biomarkers in patients with ocular surface diseases like dry eye and Sjogren’s keratoconjunctivitis sicca. 
Dr.Ping Situ
Our main goal is to advance the understanding of the neurological basis of dry eye disease using a combination of psychophysical, physiological and imaging approaches. My primary research interests include A) sensory function of the ocular surface and its role in dry eye disease and contact lens discomfort, B) psychophysical assessment of ocular surface sensation and pain, and C) the impact of tear film dynamics on ocular surface sensation.
Imaging tear film dynamics.
