lisa a. miller, phd · 2018. 7. 17. · lisa a. miller, phd my research program is focused on...

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The mission of the CNPRC is to improve human health and quality of life through support of exceptional nonhuman primate research programs. LISA A. MILLER, PhD My research program is focused on investigating the short and long-term impact of environmental exposures (air pollution, allergens, microbes) on pulmonary and immune system development during the first year of life. Our goal is to understand the molecular determinants of susceptibility in the human infant that initiate pediatric airways disease and lead to chronic pulmonary disorders in adulthood. Identification of the early life mechanisms that direct pathogenesis of lung disease at the cellular level may lead to predictive biomarkers for diagnostics and ultimately, preventative therapies. To contact Dr. Lisa Miller and for more information on her research, see: http://www.cnprc.ucdavis.edu/lisa-a-miller/ Pediatric Pulmonary Disease Core Scientist and Respiratory Diseases Unit Leader Professor Department of Anatomy, Physiology, and Cell Biology UC Davis School of Veterinary Medicine The overall goal of my research is to understand the mechanisms of susceptibility in the human infant that contribute to pediatric airways dysfunction, which may ultimately lead to generation of new diagnostics and preventive therapies. Recent studies funded by the California Air Resources Board indicate that early life exposure to wildfire smoke can be detrimental to normal development of immunity and lung function. Enhanced viral replication and modulated innate immune responses in infant airway epithelium following H1N1 infection Clay CC, Reader JR, Gerriets JE, Wang TT, Harrod KS, Miller LA J. Virol., 88:7412-7425, 2014 Early life ozone exposure results in dysregulated innate immune function and altered microRNA expression in airway epithelium. Clay CC, Maniar-Hew K, Gerriets JE, Wang TT, Postlethwait EM, Evans MJ, Fontaine JH, Miller LA Plos One, (3):e90401, 2014

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Page 1: LISA A. MILLER, PhD · 2018. 7. 17. · LISA A. MILLER, PhD My research program is focused on investigating the short and long-term impact of environmental exposures (air pollution,

The mission of the CNPRC is to improve human health and quality of life through support of exceptional

nonhuman primate research programs.

LISA A. MILLER, PhD

My research program is focused on investigating the short and long-term impact of environmental exposures (air pollution, allergens, microbes) on pulmonary and immune system development during the first year of life. Our goal is to understand the molecular determinants of susceptibility in the human infant that initiate pediatric airways disease and lead to chronic pulmonary disorders in adulthood. Identification of the early life mechanisms that direct pathogenesis of lung disease at the cellular level may lead to predictive biomarkers for diagnostics and ultimately, preventative therapies.

To contact Dr. Lisa Miller and for more information on her research, see: http://www.cnprc.ucdavis.edu/lisa-a-miller/

Pediatric Pulmonary Disease

Core Scientist and Respiratory Diseases Unit LeaderProfessor Department of Anatomy, Physiology, and Cell BiologyUC Davis School of Veterinary Medicine

The overall goal of my research

is to understand the mechanisms

of susceptibility in the human

infant that contribute to

pediatric airways dysfunction,

which may ultimately lead to

generation of new diagnostics

and preventive therapies.

Recent studies funded by the California Air Resources Board indicate that early life exposure to wildfire smoke can be detrimental to normal development of immunity and lung function.

Enhanced viral replication and modulated innate immune responses in infant airway epithelium following H1N1 infection Clay CC, Reader JR, Gerriets JE, Wang TT, Harrod KS, Miller LA J. Virol., 88:7412-7425, 2014

Early life ozone exposure results in dysregulated innate immune function and altered microRNA expression in airway epithelium. Clay CC, Maniar-Hew K, Gerriets JE, Wang TT, Postlethwait EM, Evans MJ, Fontaine JH, Miller LAPlos One, (3):e90401, 2014