Lakshman Varanasi

Assistant Professor of Biological Sciences at Krea University
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Contact Information
us****@****om
(386) 825-5501
Location
Hyderabad, Telangana, India, IN

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Credentials

  • NIDA, Clinical Trials Network, NIH, Certificate of completion of course on Good Clinical Practice (GCP)
    National Institue on Drug Abuse (NIDA), Center for Clinical Trials (CCTN), Nation Institutes of Health (NIH), USA
    Nov, 2019
    - Oct, 2024

Experience

    • India
    • Higher Education
    • 100 - 200 Employee
    • Assistant Professor of Biological Sciences
      • Mar 2021 - Present
    • Science Associate
      • Sep 2020 - Dec 2020
    • India
    • Hospitals and Health Care
    • 1 - 100 Employee
    • Head, Life Sciences Research
      • Feb 2020 - Jun 2020
    • India
    • IT Services and IT Consulting
    • 1 - 100 Employee
    • Chief Operating Officer
      • Dec 2019 - Feb 2020

    • Chief Advisor, Biomedicine
      • Jan 2019 - Dec 2019

    • Researcher
      • Apr 2018 - Dec 2018
    • Postdoctoral Research Fellow
      • Jun 2013 - Apr 2017

      The larger goal of my work is to identify protein indicators of neoplastic diseases of the gut in patient serum. We use mice that have been grafted with human tumor tissue to simulate the actual disease. Proteins leaked or secreted by the tumor in trace quantities into the mouse’s bloodstream are likely to be attributes of the disease, its presence and its intensity and progression. Mouse serum is collected after the tumor reaches a certain size, enriched for glycosylated proteins and analyzed… Show more The larger goal of my work is to identify protein indicators of neoplastic diseases of the gut in patient serum. We use mice that have been grafted with human tumor tissue to simulate the actual disease. Proteins leaked or secreted by the tumor in trace quantities into the mouse’s bloodstream are likely to be attributes of the disease, its presence and its intensity and progression. Mouse serum is collected after the tumor reaches a certain size, enriched for glycosylated proteins and analyzed in the mass spectrometer. Acquired tandem mass spectra are read by in-house software and a list of identifications is compiled. The process has yielded several protein markers, some of which are novel. The quantities of these proteins will be measured in collected sera from a large cohort of patients and healthy individuals. If the candidate marker is not present in equal measure in the two populations, after correcting for natural variation, it is deemed to have clinical value. Such proteins will be correlated with the duration and quality of patient survival to determine if one or more of them can aid disease prognosis. Show less The larger goal of my work is to identify protein indicators of neoplastic diseases of the gut in patient serum. We use mice that have been grafted with human tumor tissue to simulate the actual disease. Proteins leaked or secreted by the tumor in trace quantities into the mouse’s bloodstream are likely to be attributes of the disease, its presence and its intensity and progression. Mouse serum is collected after the tumor reaches a certain size, enriched for glycosylated proteins and analyzed… Show more The larger goal of my work is to identify protein indicators of neoplastic diseases of the gut in patient serum. We use mice that have been grafted with human tumor tissue to simulate the actual disease. Proteins leaked or secreted by the tumor in trace quantities into the mouse’s bloodstream are likely to be attributes of the disease, its presence and its intensity and progression. Mouse serum is collected after the tumor reaches a certain size, enriched for glycosylated proteins and analyzed in the mass spectrometer. Acquired tandem mass spectra are read by in-house software and a list of identifications is compiled. The process has yielded several protein markers, some of which are novel. The quantities of these proteins will be measured in collected sera from a large cohort of patients and healthy individuals. If the candidate marker is not present in equal measure in the two populations, after correcting for natural variation, it is deemed to have clinical value. Such proteins will be correlated with the duration and quality of patient survival to determine if one or more of them can aid disease prognosis. Show less

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Postdoctoral Research Fellow
      • Aug 2010 - Mar 2013

Education

  • University of Mississippi Medical Center
    Doctor of Philosophy (Ph.D.), Biochemistry
    2004 - 2010
  • Jawaharlal Nehru University
    Master of Science - MS, Life Sciences
    2002 - 2004
  • Bharathiya Vidya Bhavans Vivekananda College of Science, Humanities & Commerce
    Bachelor of Science - BSc, Biochemistry, Microbiology and Chemistry
    1999 - 2002
  • Little Flower Junior College, Hyderabad
    1996 - 1998
  • Loyola School Jamshedpur
    1985 - 1996

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