Dinesh Kumar

Dr. Dinesh Kumar

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Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

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

Representative Publications

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17 July 2014 in ChemMedChem
Verified
Journal Article
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AGAnirban Ghosh
Anirban Ghosh
RKRajiv K. Kar
Rajiv K. Kar
JJJagannath Jana
Jagannath Jana
ASAbhijit Saha
Abhijit Saha
BJBatakrishna Jana
Batakrishna Jana
ABAnirban Bhunia
Anirban Bhunia

14 October 2016 in Scientific Reports
Verified
Journal Article
Open access
AGAnupam Guleria
Anupam Guleria
APAvadhesh Pratap
Avadhesh Pratap
DDDurgesh Dubey
Durgesh Dubey
ARAtul Rawat
Atul Rawat
SCSmriti Chaurasia
Smriti Chaurasia
DKDinesh Kumar
Dinesh Kumar
Management of patient with Lupus Nephritis (LN) continues to remain a challenge for the treating physicians because of considerable morbidity and even mortality. The search of biomarkers in serum and urine is a focus of researchers to unravel new targets for therapy. In the present study, the utility of NMR-based serum metabolomics has been evaluated for the first time in discriminating LN patients from non-nephritis lupus patients (SLE) and further to get new insights into the underlying disease processes for better clinical management. Metabolic profiling of sera obtained from 22 SLE patients, 40 LN patients and 30 healthy controls (HC) were performed using high resolution 1D1H-CPMG and diffusion edited NMR spectra to identify the potential molecular biomarkers. Using multivariate analysis, we could distinguish SLE and LN patients from HC and LN from SLE patients. Compared to SLE patients, the LN patients had increased serum levels of lipid metabolites (including LDL/VLDL lipoproteins), creatinine and decreased levels of acetate. Our results revealed that metabolic markers especially lipids and acetate derived from NMR spectroscopy has high sensitivity and specificity to distinguish LN among SLE patients and has the potential to be a useful adjunctive tool in diagnosis and clinical management of LN.

1 January 2018 in Chemico-Biological Interactions
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Journal Article
Closed access
ASASHOK KUMAR SINGH
ASHOK KUMAR SINGH
VRVinit Raj
Vinit Raj
AKAmit K. Keshari
Amit K. Keshari
ARAmit Rai
Amit Rai
PKPranesh Kumar
Pranesh Kumar
SSSudipta Saha
Sudipta Saha

25 July 2017 in Oncotarget
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Journal Article
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SRSubhadeep Roy
Subhadeep Roy
ARAtul Kumar Rawat
Atul Kumar Rawat
SSShreesh Raj Sammi
Shreesh Raj Sammi
UDUma Devi
Uma Devi
MSManjari Singh
Manjari Singh
GKGaurav Kaithwas
Gaurav Kaithwas
Alpha-linolenic acid stabilizes HIF-1 and downregulates FASN to promote mitochondrial apoptosis for mammary gland chemoprevention Alpha-linolenic acid stabilizes HIF-1 α and downregulates FASN to promote mitochondrial apoptosis for mammary gland chemoprevention

1 April 2016 in Journal of Ethnopharmacology
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Journal Article
Closed access
AKAmit K. Keshari
Amit K. Keshari
GKGhanendra Kumar
Ghanendra Kumar
PKPriya S. Kushwaha
Priya S. Kushwaha
MBMonika Bhardwaj
Monika Bhardwaj
PKPranesh Kumar
Pranesh Kumar
SSSudipta Saha
Sudipta Saha

25 September 2018 in ACS Omega
Verified
Journal Article
Open access
Neha AroraNeha Arora
Neha Arora
DDDurgesh Dubey
Durgesh Dubey
MSMeenakshi Sharma
Meenakshi Sharma
ALOK PATELALOK PATEL
ALOK PATEL
AGAnupam Guleria
Anupam Guleria
Krishna Mohan PoluriKrishna Mohan Poluri
Krishna Mohan Poluri
Nuclear magnetic resonance (NMR)-based metabolomic approach is a high-throughput fingerprinting technique that allows a rapid snapshot of metabolites without any prior knowledge of the organism. To demonstrate the applicability of NMR-based metabolomics in the field of microalgal-based bioremediation, novel freshwater microalga Scenedesmus sp. IITRIND2 that showed hypertolerance to As(III, V) was chosen for evaluating the metabolic perturbations during arsenic stress in both its oxidation states As(III) and As(V). Using NMR spectroscopy, we were able to identify and quantify an array of ∼45 metabolites, including amino acids, sugars, organic acids, phosphagens, osmolytes, nucleotides, etc. The NMR metabolomic experiments were complemented with various biophysical techniques to establish that the microalga tolerated the arsenic stress using a complex interplay of metabolites. The two different arsenic states distinctly influenced the microalgal cellular mechanisms due to their altered physicochemical properties. Eighteen differentially identified metabolites related to bioremediation of arsenic were then correlated to the major metabolic pathways to delineate the variable stress responses of microalga in the presence of As(III, V).