Chandra S Verma

Dr. Chandra S Verma

orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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18 December 2012 in ACS Chemical Biology
Verified
Journal Article
Closed access
CBChristopher J. Brown
Christopher J. Brown
SQSoo T. Quah
Soo T. Quah
JJJanice Jong
Janice Jong
AGAmanda M. Goh
Amanda M. Goh
PCPoh C. Chiam
Poh C. Chiam
DLDavid Lane
David Lane

7 November 2006 in Nucleic Acids Research
Verified
Journal Article
Open access
PDF file
SSShalin Seebah
Shalin Seebah
ASAnita Suresh
Anita Suresh
SZShaowei Zhuo
Shaowei Zhuo
YCYong How Choong
Yong How Choong
HCHazel Chua
Hazel Chua
CVChandra S Verma
Chandra S Verma
The defensins knowledgebase is a manually curated database and information source focused on the defensin family of antimicrobial peptides. The current version of the database holds a comprehensive collection of over 350 defensin records each containing sequence, structure and activity information. A web-based interface provides access to the information and allows for text-based searching on the data fields. In addition, the website presents information on patents, grants, research laboratories and scientists, clinical studies and commercial entities pertaining to defensins. With the rapidly increasing interest in defensins, we hope that the knowledgebase will prove to be a valuable resource in the field of antimicrobial peptide research. The defensins knowledgebase is available at .

1 February 2008 in EMBO Reports
Verified
Journal Article
Open access
PDF file
GDGuy G Dodson
Guy G Dodson
DLDavid Lane
David Lane
CVChandra S Verma
Chandra S Verma
Recent advances in computer hardware and software have led to the development of increasingly successful molecular simulations of protein structural dynamics that are intrinsic to biological processes. These simulations have resulted in models that increasingly agree with experimental observations, suggest new experiments and provide insights into biological mechanisms. Used in combination with data obtained with sophisticated experimental techniques, simulations are helping us to understand biological complexity at the atomic and molecular levels and are giving promising insights into the genetic, thermodynamic and functional/mechanistic behaviour of biological processes. Here, we highlight some examples of such approaches that illustrate the current state and potential of the field of molecular simulation.

24 June 2021 in Journal of Chemical Information and Modeling
Verified
Journal Article
Closed access
PAPietro G.A. Aronica
Pietro G.A. Aronica
LRLauren M. Reid
Lauren M. Reid
NDNirali Desai
Nirali Desai
Jianguo LiJianguo Li
Jianguo Li
SFStephen J. Fox
Stephen J. Fox
CVChandra S Verma
Chandra S Verma

1 October 2016 in Drug Discovery Today
Verified
Journal Article
Closed access
Yaw Sing TanYaw Sing Tan
Yaw Sing Tan
DLDavid Lane
David Lane
CVChandra S Verma
Chandra S Verma

28 May 2019 in Cancers
Verified
Journal Article
Open access
PDF file
DCDenis Collins
Denis Collins
NCNeil Conlon
Neil Conlon
SKSrinivasaraghavan Kannan
Srinivasaraghavan Kannan
CVChandra S Verma
Chandra S Verma
LELisa D. Eli
Lisa D. Eli
JCJohn Crown
John Crown
An estimated 15–20% of breast cancers overexpress human epidermal growth factor receptor 2 (HER2/ERBB2/neu). Two small-molecule tyrosine kinase inhibitors (TKIs), lapatinib and neratinib, have been approved for the treatment of HER2-positive (HER2+) breast cancer. Lapatinib, a reversible epidermal growth factor receptor (EGFR/ERBB1/HER1) and HER2 TKI, is used for the treatment of advanced HER2+ breast cancer in combination with capecitabine, in combination with trastuzumab in patients with hormone receptor-negative metastatic breast cancer, and in combination with an aromatase inhibitor for the first-line treatment of HER2+ breast cancer. Neratinib, a next-generation, irreversible pan-HER TKI, is used in the US for extended adjuvant treatment of adult patients with early-stage HER2+ breast cancer following 1 year of trastuzumab. In Europe, neratinib is used in the extended adjuvant treatment of adult patients with early-stage hormone receptor-positive HER2+ breast cancer who are less than 1 year from the completion of prior adjuvant trastuzumab-based therapy. Preclinical studies have shown that these agents have distinct properties that may impact their clinical activity. This review describes the preclinical characterization of lapatinib and neratinib, with a focus on the differences between these two agents that may have implications for patient management.