Nichola C. Garbett

Dr. Nichola C. Garbett

UofL Health—Brown Cancer Center and Division of Medical Oncology and Hematology, Department of Medicine, University of Louisville, Louisville, KY 40202, USA
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Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 March 2012 in Expert Opinion on Drug Discovery
Verified
Journal Article
Closed access
NGNichola C. Garbett
Nichola C. Garbett
JCJonathan B Chaires
Jonathan B Chaires
Introduction: A key part of drug design and development is the optimization of molecular interactions between an engineered drug candidate and its binding target. Thermodynamic characterization pro...

8 January 2014 in PLOS ONE
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Journal Article
Open access
PDF file
NGNichola C. Garbett
Nichola C. Garbett
MMMichael L. Merchant
Michael L. Merchant
CHC. William Helm
C. William Helm
AJAlfred B. Jenson
Alfred B. Jenson
JKJon B. Klein
Jon B. Klein
JCJonathan B. Chaires
Jonathan B. Chaires
Improved methods for the accurate identification of both the presence and severity of cervical intraepithelial neoplasia (CIN) and extent of spread of invasive carcinomas of the cervix (IC) are needed. Differential scanning calorimetry (DSC) has recently been shown to detect specific changes in the thermal behavior of blood plasma proteins in several diseases. This methodology is being explored to provide a complementary approach for screening of cervical disease. The present study evaluated the utility of DSC in differentiating between healthy controls, increasing severity of CIN and early and advanced IC. Significant discrimination was apparent relative to the extent of disease with no clear effect of demographic factors such as age, ethnicity, smoking status and parity. Of most clinical relevance, there was strong differentiation of CIN from healthy controls and IC, and amongst patients with IC between FIGO Stage I and advanced cancer. The observed disease-specific changes in DSC profiles (thermograms) were hypothesized to reflect differential expression of disease biomarkers that subsequently bound to and affected the thermal behavior of the most abundant plasma proteins. The effect of interacting biomarkers can be inferred from the modulation of thermograms but cannot be directly identified by DSC. To investigate the nature of the proposed interactions, mass spectrometry (MS) analyses were employed. Quantitative assessment of the low molecular weight protein fragments of plasma and urine samples revealed a small list of peptides whose abundance was correlated with the extent of cervical disease, with the most striking plasma peptidome data supporting the interactome theory of peptide portioning to abundant plasma proteins. The combined DSC and MS approach in this study was successful in identifying unique biomarker signatures for cervical cancer and demonstrated the utility of DSC plasma profiles as a complementary diagnostic tool to evaluate cervical cancer health.

1 April 2015 in Methods
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Journal Article
Closed access
NGNichola C. Garbett
Nichola C. Garbett
CMChongkham S. Mekmaysy
Chongkham S. Mekmaysy
LDLynn DeLeeuw
Lynn DeLeeuw
JCJonathan B. Chaires
Jonathan B. Chaires

29 January 2014 in European Journal of Trauma and Emergency Surgery
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Journal Article
Closed access
PDF file
AKA. M. Kwon
A. M. Kwon
NGNichola C. Garbett
Nichola C. Garbett
GKG. H. Kloecker
G. H. Kloecker

1 May 2016 in Biochimica et Biophysica Acta (BBA) - General Subjects
Verified
Journal Article
Closed access
NGNichola C. Garbett
Nichola C. Garbett
GBGuy Brock
Guy Brock

1 August 2018 in Biochimica et Biophysica Acta (BBA) - General Subjects
Verified
Journal Article
Closed access
AVAdrian Velazquez-Campoy
Adrian Velazquez-Campoy
SVSonia Vega
Sonia Vega
OSOscar Sanchez-Gracia
Oscar Sanchez-Gracia
ALAngel Lanas
Angel Lanas
ARAlberto Rodrigo
Alberto Rodrigo
Olga AbianOlga Abian
Olga Abian