PROGRAM DIRECTORPRINCIPAL INVESTIGATOR (LAST FIRST MIDDLE) BIOGRAPHICAL SKETCH

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PHS 398/2590 (Rev. 06/09), Biographical Sketch Format Page

Program Director/Principal Investigator (Last, First, Middle):

BIOGRAPHICAL SKETCH

Provide the following information for the Senior/key personnel and other significant contributors in the order listed on Form Page 2.
Follow this format for each person. DO NOT EXCEED FOUR PAGES.


NAME: Navita Nanda-Lopez


POSITION TITLE: Graduate Teaching Assistant


eRA COMMONS USER NAME (credential, e.g., agency login)


EDUCATION/TRAINING (Begin with baccalaureate or other initial professional education, such as nursing, include postdoctoral training and residency training if applicable.)

INSTITUTION AND LOCATION

DEGREE

(if applicable)

MM/YY

FIELD OF STUDY

Kings College London


Randall Division of Cell and Molecular Biophysics


Kings College London


MRC centre for Developmental Neurobiology


University of North Texas Health Science Center

BSc


N/A

MSc


N/A


PhD

08/2008


07/2008


09/2011


09/2011


Present

Biomedical Science (neuroscience)

Research Student


Developmental Neurobiology

Research Student


Visual Sciences


















NOTE: The Biographical Sketch may not exceed four pages. Follow the formats and instructions below.

  1. Personal Statement


I am a first year graduate student currently in core classes and have completed my first rotation at the North Texas Eye Research Institute (NTERI) with co-mentors Dr Clark and Dr Tovar-Vidales. I initially started a position as a research assistant decided to continue my graduate education at UNTHSC, specialising in visual sciences. I have a broad background in developmental biology which led me to develop an interest in glaucoma pathophysiology. Glaucoma is a progressive optic neuropathy causing irreversible vision loss. I want to study the developmental glaucomatous changes that occur. Elevated intraocular pressure (IOP) is a major risk factor associated with glaucoma (Gordon et al, 2002) and is due to increased aqueous humor outflow resistance (Rohen JW, 1983). This increased pressure causes remodeling of the optic nerve head (ONH) cells. I am interested in optic nerve head astrocytes and lamina cribrosa cells and their involvement in glaucoma pathophysiology. My research will involve the effect of TGFβ2 on differences in miRNAs in ONH cells and to understand associated changes in normal tissue and glaucoma pathophysiology. In my second rotation I will study aqueous humor dynamics.


Science is a journey of discovery and progress depends on interactions. NTERI is a great scientific community with different cultures and backgrounds. One of my passions in exploring cultures and arts of the world through travelling with my family and friends.

B. Positions and Honors

Positions and Employment

2013-2015 Research Assistant, Department of Neuroscience and Pharmacology, UNTHSC, Fort Worth TX

2013-2015 Brain Bank Manager, Institute for Aging and Alzheimer’s Disease Research, UNTHSC, Fort Worth TX

2011-2013 Tutor (Calculus I/II, Precalculus, Geometry, Biology and Chemistry), Dallas, TX and London, United Kingdom


Honors

2008 Fredrick Wood Science Award, Kings College London, United Kingdom

C. Selected Peer-reviewed Publications

D. Research Support


PHS 398/2590 (Rev. 06/09) Page Biographical Sketch Format Page


  PROGRAMA DE ACTIVIDADES EN BODEGA VISITA GUIADA
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 DOKUZ EYLÜL ÜNİVERSİTESİ FARABİ DEĞİŞİM PROGRAMI ÖĞRENİM PROTOKOLÜ


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