Wednesday, July 11, 2018

Withania somnifera Published articles अश्वगंधा அமுக்கிரா అశ్వగంధ ಅಶ್ವಗಂಧಾ അമുക്കുരം અશ્વગંધા ਅਸ਼ਵਗੰਧਾ


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http://medplants.blogspot.com/2018/07/withania-somnifera.html

1.    Vinay, K., N.A. Gajbhiye, and P. Manivel, Assessment of the genetic diversity of Ashwagandha (Withania somnifera L. Dunal) using agro-morphological, phytochemical and molecular markers. Research Journal of Biotechnology, 2018. 13(7): p. 59-68.
2.    Sudeep, H.V., et al., Viwithan, a Standardized Withania somnifera Root Extract Induces Apoptosis in Murine Melanoma Cells. Pharmacognosy magazine, 2018. 13(Suppl 4): p. S801-S806.
3.    Srivastava, S., et al., Comparative Study of Withanolide Biosynthesis-Related miRNAs in Root and Leaf Tissues of Withania somnifera. Applied biochemistry and biotechnology, 2018.
4.    Srivastava, A., et al., Genetic variability, associations, and path analysis of chemical and morphological traits in Indian ginseng Withania somnifera (L.) Dunal for selection of higher yielding genotypes. Journal of Ginseng Research, 2018. 42(2): p. 158-164.
5.    Sood, A., et al., Indian Ginseng (Withania somnifera) supplementation ameliorates oxidative stress and mitochondrial dysfunctions in experimental model of stroke. Metabolic brain disease, 2018.
6.    Singh, R., et al., Modulations in primary and secondary metabolic pathways and adjustment in physiological behaviour of Withania somnifera under drought stress. Plant science : an international journal of experimental plant biology, 2018. 272: p. 42-54.
7.    Shasmita, M.K. Rai, and S.K. Naik, Exploring plant tissue culture in Withania somnifera (L.) Dunal: in vitro propagation and secondary metabolite production. Critical Reviews in Biotechnology, 2018. 38(6): p. 836-850.
8.    Sharma, R., et al., Adaptive physiological response, carbon partitioning, and biomass production of Withania somnifera (L.) Dunal grown under elevated CO2 regimes. 3 Biotech, 2018. 8(6).
9.    Sengupta, P., et al., Role of Withania somnifera (Ashwagandha) in the management of male infertility. Reproductive Biomedicine Online, 2018. 36(3): p. 311-326.
10.    Sathiyabama, M. and R. Parthasarathy, Withanolide production by fungal endophyte isolated from Withania somnifera. Natural Product Research, 2018. 32(13): p. 1573-1577.
11.    Pandey, S.S., et al., Endophytes of Withania somnifera modulate in planta content and the site of withanolide biosynthesis. Scientific Reports, 2018. 8.
12.    Pandey, A., et al., Multifunctional neuroprotective effect of Withanone, a compound from Withania somnifera roots in alleviating cognitive dysfunction. Cytokine, 2018. 102: p. 211-221.
13.    Nasimi Doost Azgomi, R., et al., Comparative evaluation of the effects of Withania somnifera with pentoxifylline on the sperm parameters in idiopathic male infertility: A triple-blind randomised clinical trial. Andrologia, 2018: p. e13041-e13041.
14.    Naidoo, D.B., et al., Withania somnifera modulates cancer cachexia associated inflammatory cytokines and cell death in leukaemic THP-1 cells and peripheral blood mononuclear cells (PBMC's). Bmc Complementary and Alternative Medicine, 2018. 18.
15.    Mishra, A., et al., Endophyte-Mediated Modulation of Defense-Related Genes and Systemic Resistance in Withania somnifera (L.) Dunal under Alternaria alternata Stress. Applied and Environmental Microbiology, 2018. 84(8).
16.    Mishra, A., et al., Bacterial endophytes modulates the withanolide biosynthetic pathway and physiological performance in Withania somnifera under biotic stress. Microbiological research, 2018. 212-213: p. 17-28.
17.    Mahrous, R.S.R., et al., Validated thin-layer chromatographic method for the identification and monitoring of the effect of the extraction method on the yield and phytochemical constituents of Egyptian Withania somnifera leaves. Journal of Separation Science, 2018. 41(2): p. 518-524.
18.    Lim, D.W., et al., Antihyperalgesic effects of ashwagandha (Withania somnifera root extract) in rat models of postoperative and neuropathic pain. Inflammopharmacology, 2018. 26(1): p. 207-215.
19.    Kumar, S., et al., Extraction Optimization for Phenolic- and Withanolide-Rich Fractions from Withania somnifera Roots: Identification and Quantification of Withaferin A, 12-Deoxywithastromonolide, and Withanolide A in Plant Materials and Marketed Formulations Using a Reversed-Phase HPLC-Photodiode Array Detection Method. Journal of AOAC International, 2018.
20.    Kumar, R., et al., Comparative study of effect of Withania somnifera as an adjuvant to DOTS in patients of newly diagnosed sputum smear positive pulmonary tuberculosis. The Indian journal of tuberculosis, 2018. 65(3): p. 246-251.
21.    Johny, L., et al., Growth kinetics and withanolide production in novel transformed roots of Withania somnifera and measurement of their antioxidant potential using chemiluminescence. Plant Cell Tissue and Organ Culture, 2018. 132(3): p. 479-495.
22.    Jain, J., et al., In Vivo Evaluation of Withania somnifera-Based Indian Traditional Formulation ( Amukkara Choornam), Against Chikungunya Virus-Induced Morbidity and Arthralgia. Journal of evidence-based integrative medicine, 2018. 23: p. 2156587218757661-2156587218757661.
23.    Hameed, A. and N. Akhtar, Comparative chemical investigation and evaluation of antioxidant and tyrosinase inhibitory effects of Withania somnifera (L.) Dunal and Solanum nigrum (L.) berries. Acta Pharmaceutica, 2018. 68(1): p. 47-60.
24.    Gupta, M. and G. Kaur, Withania somnifera as a Potential Anxiolytic and Anti-inflammatory Candidate Against Systemic Lipopolysaccharide-Induced Neuroinflammation. Neuromolecular medicine, 2018.
25.    George, B.S., et al., Characterization of an Insecticidal Protein from Withania somnifera Against Lepidopteran and Hemipteran Pest. Molecular Biotechnology, 2018. 60(4): p. 290-301.
26.    Elhadidy, M.E., et al., Protective effect of ashwagandha (Withania somnifera) against neurotoxicity induced by aluminum chloride in rats. Asian Pacific Journal of Tropical Biomedicine, 2018. 8(1): p. 59-66.
27.    Deshpande, A., N. Irani, and R. Balakrishnan, Study protocol and rationale for a prospective, randomized, double-blind, placebo-controlled study to evaluate the effects of Ashwagandha (Withania somnifera) extract on nonrestorative sleep. Medicine, 2018. 97(26): p. e11299-e11299.
28.    Caputi, F.F., et al., The standardized Withania somnifera Dunal root extract alters basal and morphine-induced opioid receptor gene expression changes in neuroblastoma cells. Bmc Complementary and Alternative Medicine, 2018. 18.
29.    Azgomi, R.N.D., et al., Effects of Withania somnifera on Reproductive System: A Systematic Review of the Available Evidence. Biomed Research International, 2018.
30.    Alrashidi, A.A., E.A. Kalashnikova, and R.N. Kirakosyan, THE PREPARATION AND CHARACTERIZATION OF SUSPENSION CELL CULTURES OF WITHANIA SOMNIFERA L. Voprosy biologicheskoi, meditsinskoi i farmatsevticheskoi khimii, 2018. 21(3): p. 32-36.
31.    Akhtar, R. and A. Javaid, BIOLOGICAL MANAGEMENT OF BASAL ROT OF ONION BY Trichoderma harzianum AND Withania somnifera. Planta Daninha, 2018. 36.
32.    Ahmed, W., et al., Antioxidant activity and apoptotic induction as mechanisms of action of Withania somnifera (Ashwagandha) against a hepatocellular carcinoma cell line. Journal of International Medical Research, 2018. 46(4): p. 1358-1369.
33.    Agarwal, A.V., et al., Virus-Induced Silencing of Key Genes Leads to Differential Impact on Withanolide Biosynthesis in the Medicinal Plant, Withania somnifera. Plant and Cell Physiology, 2018. 59(2): p. 262-274.
34.    Abul Qais, F., Samreen, and I. Ahmad, Broad-spectrum inhibitory effect of green synthesised silver nanoparticles from Withania somnifera (L.) on microbial growth, biofilm and respiration: a putative mechanistic approach. Iet Nanobiotechnology, 2018. 12(3): p. 325-335.
35.    Zaka, M., et al., Comparative in silico analyses of Cannabis sativa, Prunella vulgaris and Withania somnifera compounds elucidating the medicinal properties against rheumatoid arthritis. Journal of Molecular Graphics & Modelling, 2017. 74: p. 296-304.
36.    Trivedi, M.K., et al., Metabolite Profiling in Withania somnifera Roots Hydroalcoholic Extract Using LC/MS, GC/MS and NMR Spectroscopy. Chemistry & Biodiversity, 2017. 14(3).
37.    Trivedi, M.K., et al., Immunomodulatory properties and biomarkers characterization of novel Withania somnifera based formulation supplemented with minerals in Sprague Dawley rats. Oriental Pharmacy and Experimental Medicine, 2017. 17(1): p. 59-69.
38.    Tripathi, S., et al., Transcription factor repertoire in Ashwagandha (Withania somnifera) through analytics of transcriptomic resources: Insights into regulation of development and withanolide metabolism. Scientific Reports, 2017. 7.
39.    Tripathi, C.D.P., et al., Withania somnifera chemotype NMITLI 101R significantly increases the efficacy of antileishmanial drugs by generating strong IFN-gamma and IL-12 mediated immune responses in Leishmania donovani infected hamsters. Phytomedicine, 2017. 24: p. 87-95.
40.    Thakur, S., et al., Nutritional enrichment of broiler breast meat through dietary supplementation of Indian ginseng Withania somnifera and synbiotic substances under semi-arid climatic conditions. Veterinary World, 2017. 10(11): p. 1301-1306.
41.    Tarique, A., et al., Preventive role of Withania somnifera on hyperlipidemia and cardiac oxidative stress in streptozotocin induced type 2 diabetic rats. Tropical Journal of Pharmaceutical Research, 2017. 16(1): p. 119-125.
42.    Takshak, S. and S.B. Agrawal, Exogenous application of IAA alleviates effects of supplemental ultraviolet-B radiation in the medicinal plant Withania somnifera Dunal. Plant Biology, 2017. 19(6): p. 904-916.
43.    Takshak, S. and S.B. Agrawal, Effect of supplemental ultraviolet-B radiation on Withania somnifera L. (Dunal): An appraisal of morphological, physiological and biochemical characteristics. Indian Journal of Experimental Biology, 2017. 55(12): p. 845-852.
44.    Sumaira, A., et al., Current status of Withania somnifera (L.) dunal: an endangered medicinal plant from Himalaya. American Journal of Plant Sciences, 2017. 8(5): p. 1159-1169.
45.    Sood, A. and R. Sandhir, Neuroprotective potential of Withania somnifera prophylaxis in experimental stroke reasearch. Cerebrovascular Diseases, 2017. 43.
46.    Solanki, S. and D. Basudeb, First report of leaf spot of Aswagandha (Withania somnifera Dunal) caused by Colletotrichum gloeosporioides from West Bengal, India. Journal of Mycopathological Research, 2017. 55(3): p. 257-259.
47.    Singla, M., et al., Impact of Ashwagandha (Withania somnifera) supplementation on the performance of Beetal kids under stall-fed conditions. Indian Journal of Animal Research, 2017. 51(6): p. 1086-1090.
48.    Singh, V., et al., Leaf spot disease adversely affects human health-promoting constituents and withanolide biosynthesis in Withania somnifera (L.) Dunal. Journal of Applied Microbiology, 2017. 122(1): p. 153-165.
49.    Singh, V., et al., Changes in the leaf proteome profile of Withania somnifera (L.) Dunal in response to Alternaria alternata infection. Plos One, 2017. 12(6).
50.    Singh, P., et al., Addressing Challenges to Enhance the Bioactives of Withania somnifera through Organ, Tissue, and Cell Culture Based Approaches. Biomed Research International, 2017.
51.    Singh, M.K., et al., Effect of dietary supplementation of Ashwagandha (Withania somnifera) and Selenium on growth performance and carcass quality of broilers. Asian Journal of Animal Science, 2017. 12(2): p. 129-133.
52.    Singh, M. and C. Ramassamy, In vitro screening of neuroprotective activity of Indian medicinal plant Withania somnifera. Journal of Nutritional Science, 2017. 6.
53.    Singh, G., et al., Sterol glycosyltransferases required for adaptation of Withania somnifera at high temperature. Physiologia Plantarum, 2017. 160(3): p. 297-311.
54.    Singh, G., et al., Effect of antioxidant protection system on regeneration potential of different chemotypes of Withania somnifera (L.) Dunal-A comparative analysis. Indian Journal of Experimental Biology, 2017. 55(4): p. 242-250.
55.    Singh, A.K., et al., A WRKY transcription factor from Withania somnifera regulates triterpenoid withanolide accumulation and biotic stress tolerance through modulation of phytosterol and defense pathways. New Phytologist, 2017. 215(3): p. 1115-1131.
56.    Sharma, D., V. Roy, and A. Saraf, An Update on Phytochemicals Analysis and Medicinal Prospects of Indian Herb Withania somnifera. Ambient Science, 2017. 4(2).
57.    Shah, R.A., et al., EVALUATION OF ANTIDIABETIC POTENTIAL OF WITHANIA SOMNIFERA BY GLUCOSE UPTAKE ASSAY ON 3T3 F442A FIBROBLAST (ADIPOCYTE) CELLS. International Journal of Pharmaceutical Sciences and Research, 2017. 8(1): p. 120-125.
58.    Shaffi, M. and K. Gurcharan, Withania somnifera leaf alleviates cognitive dysfunction by enhancing hippocampal plasticity in high fat diet induced obesity model. BMC Complementary and Alternative Medicine, 2017. 17(136): p. (3 March 2017)-(3 March 2017).
59.    Saykally, J.N., et al., Withania somnifera Extract Protects Model Neurons from In Vitro Traumatic Injury. Cell Transplantation, 2017. 26(7): p. 1193-1201.
60.    Saxena, P., et al., Gene expression analysis of the withanolide biosynthetic pathway in hairy root cultures of Withania somnifera elicited with methyl jasmonate and the fungus Piriformospora indica. Symbiosis, 2017. 71(2): p. 143-154.
61.    Reddy, K.B. and R.K. Jat, Isolation and characterization of Withaferin-A from the Withania somnifera (Ashwagandha). Journal of Drug Delivery and Therapeutics, 2017. 7(1): p. 65-69.
62.    Razdan, S., et al., Molecular characterization of DWF1 from Withania somnifera (L.) Dunal: its implications in withanolide biosynthesis. Journal of Plant Biochemistry and Biotechnology, 2017. 26(1): p. 52-63.
63.    Raju, S.K., et al., A study on the anticonvulsant activity of Withania somnifera (Dunal) in albino rats. National Journal of Physiology, Pharmacy and Pharmacology, 2017. 7(1): p. 17-21.
64.    Pradhan, R., et al., Longevity and healthy ageing genes FOXO3A and SIRT3: Serum protein marker and new road map to burst oxidative stress by Withania somnifera. Experimental Gerontology, 2017. 95: p. 9-15.
65.    Pandey, V., et al., Withania somnifera : Advances and Implementation of Molecular and Tissue Culture Techniques to Enhance Its Application. Frontiers in Plant Science, 2017. 8.
66.    Pal, S., et al., Nitrogen treatment enhances sterols and withaferin A through transcriptional activation of jasmonate pathway, WRKY transcription factors, and biosynthesis genes in Withania somnifera (L.) Dunal. Protoplasma, 2017. 254(1): p. 389-399.
67.    Nikhil, M., et al., Effect of integrated nutrient management on growth, yield and quality of Ashwagandha (Withania somnifera (L.) Dunal.). Environment and Ecology, 2017. 35(4B): p. 3206-3210.
68.    Mukherjee, S., G. Kumar, and R. Patnaik, Identification of potential inhibitors of PARP-1, a regulator of caspase-independent cell death pathway, from Withania somnifera phytochemicals for combating neurotoxicity: A structure-based in-silico study. Journal of Theoretical & Computational Chemistry, 2017. 16(7).
69.    Mishra, S.K., B.A. Venkatachalapathy, and H.M. Khanli, Safety and efficacy of Ashwagandha (Withania somnifera). Neuroprotective natural products: clinical aspects and mode of action, ed. G. Brahmachari. 2017. 313-319.
70.    Mishra, M.K., et al., Overexpression of Withania somnifera SGTL1 gene resists the interaction of fungus Alternaria brassicicola in Arabidopsis thaliana. Physiological and Molecular Plant Pathology, 2017. 97: p. 11-19.
71.    Mirakzehi, M.T., S.J. Hosseini, and H. Saleh, The effects of hydroalcoholic extracts of Withania somnifera root, Withania coagulans fruit and 1,25-dihydroxycholecalciferol on immune response and small intestinal morphology of broiler chickens. Journal of Applied Animal Research, 2017. 45(1): p. 591-597.
72.    Marell, P., et al., PILOT STUDY ON THE EFFECTS OF WITHANIA SOMNIFERA ON ELECTROPHYSIOLOGICAL MEASURES OF SENSORY AND COGNITIVE PROCESSING IN SCHIZOPHRENIA. Schizophrenia Bulletin, 2017. 43: p. S185-S185.
73.    Manchanda, S., et al., Aqueous Leaf Extract of Withania somnifera as a Potential Neuroprotective Agent in Sleep-deprived Rats: a Mechanistic Study. Molecular Neurobiology, 2017. 54(4): p. 3050-3061.
74.    Manchanda, S. and G. Kaur, Withania somnifera leaf alleviates cognitive dysfunction by enhancing hippocampal plasticity in high fat diet induced obesity model. Bmc Complementary and Alternative Medicine, 2017. 17.
75.    Kumar, G. and R. Patnaik, Inhibition of Gelatinases (MMP-2 and MMP-9) by Withania somnifera Phytochemicals Confers Neuroprotection in Stroke: An In Silico Analysis. Interdisciplinary sciences, computational life sciences, 2017.
76.    Kumar, G., P. Paliwal, and R. Patnaik, Withania somnifera Phytochemicals Confer Neuroprotection by Inhibition of the Catalytic Domain of Human Matrix Metalloproteinase-9. Letters in Drug Design & Discovery, 2017. 14(6): p. 718-726.
77.    Kumar, G., et al., Withania somnifera phytochemicals confer neuroprotection by selective inhibition of nNos: An in silico study to search potent and selective inhibitors for human nNOS. Journal of Theoretical & Computational Chemistry, 2017. 16(5).
78.    Koshy, R., et al., Determination of Withanolides in Withania somnifera by Liquid Chromatography: Single-Laboratory Validation, First Action 2015.17. Journal of AOAC International, 2017. 100(1): p. 277-279.
79.    Khan, B.M., et al., Process for transformation in withania somnifera plants to increase secondary metabolite content. 2017, Council of Scientific and Industrial Research.
80.    Kaushik, M.K., et al., Triethylene glycol, an active component of Ashwagandha (Withania somnifera) leaves, is responsible for sleep induction. Plos One, 2017. 12(2).
81.    Kaur, T., et al., Withania somnifera as a potential anxiolytic and immunomodulatory agent in acute sleep deprived female Wistar rats. Molecular and Cellular Biochemistry, 2017. 427(1-2): p. 91-101.
82.    Kaur, T. and G. Kaur, Withania somnifera ameliorates neuroinflammation caused by high fat diet consumption in rat model of obesity. Journal of Neurochemistry, 2017. 142: p. 99-99.
83.    Kaur, T. and G. Kaur, Withania somnifera as a potential candidate to ameliorate high fat diet-induced anxiety and neuroinflammation. Journal of Neuroinflammation, 2017. 14.
84.    Kasar, S.S., et al., A glycoprotein alpha-amylase inhibitor from Withania somnifera differentially inhibits various alpha-amylases and affects the growth and development of Tribolium castaneum. Pest Management Science, 2017. 73(7): p. 1382-1390.
85.    Kamaljit, K., K. Gurpreet, and K. Ritesh, Withania somnifera: an important herb in ayurveda and indigenous medicinal system. Journal of Plant Science Research, 2017. 33(2): p. 209-222.
86.    Kalra, R. and N. Kaushik, Withania somnifera (Linn.) Dunal: a review of chemical and pharmacological diversity. Phytochemistry Reviews, 2017. 16(5): p. 953-987.
87.    Jeannin, J.-M., Withania somnifera. Schweizerische Zeitschrift Fuer Ganzheitsmedizin, 2017. 29(1): p. 1-1.
88.    Jadaun, J.S., et al., Over-expression of DXS gene enhances terpenoidal secondary metabolite accumulation in rose-scented geranium and Withania somnifera: active involvement of plastid isoprenogenic pathway in their biosynthesis. Physiologia Plantarum, 2017. 159(4): p. 381-400.
89.    Hussein, Y.A., S.S. Al-Shokair, and K.M. Ashry, Acute and sub-chronic toxicological potential of Withania somnifera extract on rats. Alexandria Journal of Veterinary Sciences, 2017. 55(2): p. 10-18.
90.    Henley, A.B., et al., Withania somnifera Root Extract Enhances Chemotherapy through 'Priming'. Plos One, 2017. 12(1).
91.    Hamood, A.K. and B.H. Majeed, EFFECT OF SOME PlANT GROWTH REGULATORS ON TOTAL ALKALOIDS PRODUCTION OF ASHWAGANDHA (Withania somnifera L.) In Vitro. Iraqi Journal of Agricultural Sciences, 2017. 48(3): p. 690-700.
92.    Hamood, A.K. and B.H. Majeed, EFFECT OF BENZYL ADENINE AND SALICYLIC ACID ON GROWTH AND TOTAL ALKALOIDS PRODUCTION OF WETHINIA (Withania somnifera L.) In Vitro. Iraqi Journal of Agricultural Sciences, 2017. 48(1): p. 256-265.
93.    Girish, C. and Y.N. Reddy, EVALUATION OF ANTIANAPHYLACTIC ACTIVITY OF VARIOUS EXTRACTS OF WITHANIA SOMNIFERA IN RATS. International Journal of Pharmaceutical Sciences and Research, 2017. 8(4): p. 1717-1722.
94.    Gaur, S.K. and K. Kumar, Withania somnifera acts as a potential insect growth regulator in the polyphagous pest, Pericallia ricini. Journal of Plant Protection Research, 2017. 57(4): p. 379-388.
95.    Gaur, S.K. and K. Krishna, Bioefficacy of root extracts of a medicinal plant, Withania somnifera (Dunal) against a polyphagous pest, Spodoptera litura (Fabricius) (Lepidoptera: Noctuidae). Archives of Phytopathology and Plant Protection, 2017. 50(15/16): p. 802-814.
96.    Dwivedi, D., B. Yadav, and N. Sengar, Extraction and Isolation of Withaferin A (Steroidal Lactone) from Withania somnifera Leafs and It's TLC and HPLC Analysis. Oriental Journal of Chemistry, 2017. 33(3): p. 1550-1554.
97.    Dutta, K., et al., Withania somnifera Reverses Transactive Response DNA Binding Protein 43 Proteinopathy in a Mouse Model of Amyotrophic Lateral Sclerosis/Frontotemporal Lobar Degeneration. Neurotherapeutics, 2017. 14(2): p. 447-462.
98.    Dhanani, T., et al., Effect of extraction methods on yield, phytochemical constituents and antioxidant activity of Withania somnifera. Arabian Journal of Chemistry, 2017. 10: p. S1193-S1199.
99.    Desai, C.D., et al., Effect of spacing and fertilizer levels on growth, yield and quality of Ashwagandha (Withania somnifera Dunal) cv. JA-20. International Journal of Minor Fruits, Medicinal and Aromatic Plants, 2017. 3(2): p. 8-10.
100.    Dehdashti, S.M., et al., An efficient Agrobacterium rhizogenes-mediated transformation protocol of Withania somnifera. Plant Cell Tissue and Organ Culture, 2017. 128(1): p. 55-65.
101.    Dar, N.J., et al., Withanone, an Active Constituent from Withania somnifera, Affords Protection Against NMDA-Induced Excitotoxicity in Neuron-Like Cells. Molecular Neurobiology, 2017. 54(7): p. 5061-5073.
102.    Choudhary, D., S. Bhattacharyya, and S. Bose, Efficacy and Safety of Ashwagandha (Withania somnifera (L.) Dunal) Root Extract in ImprovingMemory and Cognitive Functions. Journal of Dietary Supplements, 2017. 14(6): p. 599-612.
103.    Chinembiri, T.N., et al., Topical Delivery of Withania somnifera Crude Extracts in Niosomes and Solid Lipid Nanoparticles. Pharmacognosy Magazine, 2017. 13(51): p. S663-S671.
104.    Chaudhary, S.R., et al., Organic nutrient sources influence yield and quality of ashwagandha (Withania somnifera), and soil biochemical properties. Agrochimica, 2017. 61(3): p. 221-236.
105.    Chandrasekaran, S., et al., Alcoholic Fractions F5 and F6 from Withania somnifera Leaves Show a Potent Antileishmanial and Immunomodulatory Activities to Control Experimental Visceral Leishmaniasis. Frontiers in Medicine, 2017. 4.
106.    Chandran, U. and B. Patwardhan, Network ethnopharmacological evaluation of the immunomodulatory activity of Withania somnifera. Journal of Ethnopharmacology, 2017. 197: p. 250-256.
107.    Bhatnagar, M., et al., Complete Comparison Display (CCD) evaluation of ethanol extracts of Centella asiatica and Withania somnifera shows that they can non-synergistically ameliorate biochemical and behavioural damages in MPTP induced Parkinson's model of mice. Plos One, 2017. 12(5).
108.    Balakrishnan, A.S., et al., Withania somnifera targets interleukin-8 and cyclooxygenase-2 in human prostate cancer progression. Prostate International, 2017. 5(2): p. 75-83.
109.    Balakrishnan, A.S., R. Kalyanasundaram, and A.A. Nathan, THERAPEUTIC POTENTIAL OF WITHANIA SOMNIFERA IN FILARIAL INDUCED SECONDARY LYMPHEDEMA. American Journal of Tropical Medicine and Hygiene, 2017. 97(5): p. 563-563.
110.    Aswani, P., et al., Characterization of bioactive metabolites of endophytic Fusarium solani isolated from Withania somnifera. Journal of Biologically Active Products from Nature, 2017. 7(6): p. 411-426.
111.    Archana, K., P.M. Gangadharappa, and J.S. Hiremath, Effect of organic and inorganic sources of nutrients on root and seed yield of Ashwagandha (Withania somnifera Dunal). Environment and Ecology, 2017. 35(4D): p. 3601-3604.
112.    Anwer, T., et al., Preventive role of Withania somnifera on hyperlipidemia and cardiac oxidative stress in streptozotocin induced type 2 diabetic rats. Tropical Journal of Pharmaceutical Research, 2017. 16(1): p. 119-125.
113.    Anuroopa, N., et al., Inoculation with Selected Microbial Consortia Not Only Enhances Growth and Yield of Withania somnifera but also Reduces Fertilizer Application by 25% Under Field Conditions. Proceedings of the Indian National Science Academy, 2017. 83(4): p. 957-971.
114.    Anuroopa, N. and D.J. Bagyaraj, Selection of an Efficient Plant Growth Promoting Rhizobacteria for Inoculating Withania Somnifera. Journal of Scientific & Industrial Research, 2017. 76(4): p. 244-248.
115.    Ankad, G.M., et al., Evaluation of Kunapa jala and Pancha gavya on plant quality, physiology, biochemistry, yield and growth attributes - A case study of Withania somnifera Dun. Journal of Ayurveda and Integrative Medicine, 2017. 8(4): p. 247-251.
116.    Alrashedi, A.A., A.S. Mohamed, and R.Y. Pavlikov, INFLUENCE OF CULTIVATION CONDITIONS ON CLONAL MICRO PROPAGATION OF ASHWAGANDHA (WITANIA SOMNIFERA L.). Izvestiya Timiryazevskoi Sel'skokhozyaistvennoi Akademii, 2017(3): p. 30-38.
117.    Aljubory, I.S., et al., Pharmacognostical with preliminary phytochemical studies of Iraqi Aswagandha (withania somnifera L.) plant. Research Journal of Pharmaceutical Biological and Chemical Sciences, 2017. 8(2): p. 1934-1939.
118.    Ahmad, M. and N.J. Dar, Withania somnifera: Ethnobotany, Pharmacology, and Therapeutic Functions. Sustained Energy for Enhanced Human Functions and Activity, ed. D. Bagchi. 2017. 137-154.
119.    Ahlawat, S., et al., Comparative study of withanolide production and the related transcriptional responses of biosynthetic genes in fungi elicited cell suspension culture of Withania somnifera in shake flask and bioreactor. Plant Physiology and Biochemistry, 2017. 114: p. 19-28.
120.    Agarwal, A.V., et al., Comprehensive assessment of the genes involved in withanolide biosynthesis from Withania somnifera: chemotype-specific and elicitor-responsive expression. Functional & Integrative Genomics, 2017. 17(4): p. 477-490.
121.    Yenisetti, S.C., M.J. Manjunath, and C. Muralidhara, Neuropharmacological Properties of Withania somnifera - Indian Ginseng: An Overview on Experimental Evidence with Emphasis on Clinical Trials and Patents. Recent patents on CNS drug discovery, 2016. 10(2): p. 204-215.
122.    Vibha and U. Anubha, Effect of bioagents on Alternaria leaf spot and withaferin content of Withania somnifera (L.) Dunal. Indian Phytopathology, 2016. 69(4s): p. 333-337.
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567.    Kumar, S.S. and S. Edla, Isolation and incidence of thermophilic fungi from various thermogenic habitats in Andhra Pradesh. International Journal of Pharma and Bio Sciences, 2013. 4(4): p. B-1312-B-1318.
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590.    Halamova, K., et al., SELECTIVE IN VITRO GROWTH INHIBITORY EFFECT OF WITHANIA SOMNIFERA ON HUMAN PATHOGENIC BACTERIA AND BIFIDOBACTERIA. Pakistan Journal of Botany, 2013. 45(2): p. 667-670.
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antidysenterica Holarrhena pubescens Holoptelea integrifolia Hosta plantaginea Hoya carnosa Hydrocotyle sibthorpioides Hydrolea zeylanica Hygrophila auriculata Hygrophila polysperma Hygrophila schulli Hylocereus undatus Hymenocallis speciosa Hymenodictyon orixense Hyoscyamus niger Hypericum dyeri Hypericum elodeoides Hypericum oblongifolium Hyptis suaveolens Ilex dipyrena Impatiens balsamina Impatiens bracteata Impatiens racemosa Indigofera aspalathoides Indigofera astragalina Indigofera glabra Ipomoea alba Ipomoea aquatica Ipomoea marginata Isodon rugosus Ixeris polycephala Jacaranda mimosifolia Jacquemontia pentantha Jasminum auriculatum Jasminum multiflorum Jatropha curcas Jatropha gossypifolia Juncus thomsonii Justicia adhatoda Justicia brandegeeana Justicia carnea Justicia gendarussa Justicia pubigera Kalanchoe blossfeldiana Kallstroemia pubescens Koelreuteria elegans Koelreuteria paniculata Koenigia delicatula Kopsia fruticosa Kydia calycina Kyllinga brevifolia Lablab purpureus Lactuca dissecta Lantana camara Lathyrus sativus Leea aequata Lens culinaris Leonotis nepetifolia Leonurus cardiaca Lepidium sativum Lepisanthes rubiginosa Leucas aspera Leucas nutans Leucostemma latifolium Leycesteria formosa Ligularia amplexicaulis Ligularia fischeri Lilium polyphyllum Linum usitatissimum Liparis nervosa Liquidambar formosana Litsea monopetala Lupinus angustifolius Lycium ferocissimum Macaranga peltata Maesa argentea Magnolia champaca Mahonia napaulensis Malachra Capitata Mallotus nudiflorus Mallotus philippinensis Malva sylvestris Malvastrum coromandelianum Marchantia polymorpha Martynia annua Medicago lupulina Medicinal Plants of India Melilotus indicus Melochia corchorifolia Memecylon edule Memecylon umbellatum Mercurialis annua Meriandra strobilifera Merremia cissoides Mesua ferrea Micrococca mercuriali Micromeria biflora Mikania micrantha Millettia pinnata Mimosa polyancistra Mimosa pudica Mitragyna parvifolia Modiola caroliniana Momordica charantia Momordica cochinchinensis Morinda citrifolia Morinda pubescens Moringa oleifera Mucuna pruriens Muehlenbeckia platyclada Muehlenbeckia platyclados Muntingia calabura Murdannia nudiflora Murraya koenigii Muscari neglectum Myriactis nepalensis Myristica fragrans Myrtus communis Naravelia zeylanica Nardostachys grandiflora Nardostachys jatamansi Naringi crenulata Nasturtium officinale Nelumbo nucifera Neolamarckia cadamba Nepeta laevigata Nerium indicum Nerium oleander Nicotiana plumbaginifolia Nicotiana rustica Nicotiana tabacum Nigella sativa Nyctanthes arbor-tristis Nymphaea nouchali Nymphaea pubescens Nymphoides indica Ocimum basilicum Ocimum gratissimum Ocimum kilimandscharicum Ocimum sanctum Oldenlandia umbellata Ononis natrix Ononis repens Ononis spinosa Operculina turpethum Origanum majorana Oroxylum indicum Osteospermum ecklonis Others Oxyria digyna Pachygone ovata Pachyrhizus erosus Paederia foetida Pandanus tectorius Papaver somniferum Passiflora caerulea Passiflora vitifolia Pavetta indica Pentapetes phoenicea Pentas lanceolata Peperomia argyreia Peperomia heyneana Peperomia pellucida Peperomia sandersii Peperomia tetraphylla Perilla frutescens Persicaria amplexicaulis Persicaria barbata Persicaria capitata Persicaria glabra Persicaria nepalensis Phalaenopsis taenialis Phaulopsis dorsiflora Philodendron bipinnatifidum Phlomis bracteosa Phlomoides bracteosa Phyllanthus acidus Phyllanthus amarus Phyllanthus fraternus Phyllanthus lawii Phyllanthus rotundifolius Physalis grisea Physalis peruviana Picrorhiza kurroa Pilea microphylla Pimpinella anisum Piper betle Piper longum Piper nigrum Pisonia aculeata Pistia stratiotes Pisum sativum Plantago orbignyana Plantago ovata Platanthera edgeworthii Platostoma elongatum Plectranthus barbatus Plectranthus scutellarioides Plumbago auriculata Plumbago capensis Plumbago zeylanica Plumeria rubra Podranea ricasoliana Polemonium caeruleum Polygala crotalarioides Polygala persicariifolia Polygonatum cirrhifolium Polygonatum verticillatum Polygonum amplexicaule Polygonum barbatum Polygonum recumbens Pongamia pinnata Portulaca oleracea Portulaca umbraticola Portulacaria afra Potentilla fruticosa Potentilla supina Premna corymbosa Premna tomentosa Primula denticulata Primula floribunda Primula vulgaris Prunus Amygdalus Prunus dulcis Pseuderanthemum carruthersii Pseudobombax ellipticum Pseudocaryopteris foetida Psidium guajava Psidium guineense Pterocarpus santalinus Pterospermum acerifolium Pterospermum lanceifolium Pterygota alata Pulicaria dysenterica Punica granatum Putranjiva roxburghii Pyrostegia venusta Quisqualis indica Ranunculus arvensis Ranunculus laetus Ranunculus sceleratus Raphanus sativus Rauvolfia serpentina Rauvolfia tetraphylla Reinwardtia indica Rhamphicarpa fistulosa Rhodiola trifida Rhodiola wallichiana Rhododendron arboreum Rhynchosia heynei Rhynchosia himalensis Rhynchosia viscosa Ricinus communis Rorippa indica Roscoea purpurea Rosmarinus officinalis Ruellia patula Ruellia prostrata Ruellia tuberosa Rumex dentatus Rumex hastatus Rungia pectinata Saccharum officinarum Saccharum spontaneum Salix denticulata Salix tetrasperma Salvadora persica Salvia involucrata Salvia miltiorrhiza Salvia nubicola Salvia splendens Sambucus canadensis Sambucus mexicana Sambucus nigra Santalum album Sapindus saponaria Saussurea auriculata Saussurea candicans Saussurea obvallata Scadoxus multiflorus Scutellaria baicalensis Scutellaria grossa Scutellaria repens Sedum oreades Semecarpus anacardium Senna auriculata Senna occidentalis Senna siamea Senna sophera Sesbania bispinosa Sesbania grandiflora Seseli diffusum Sesuvium portulacastrum Setaria verticillata Shorea robusta Sida cordata Sida cordifolia Sida retusa Sida spinosa Sideritis hirsuta Silybum marianum Smithia ciliata Solanum chrysotrichum Solanum erianthum Solanum jasminoides Solanum melongena Solanum nigrum Solanum sisymbriifolium Solanum surattense Solanum torvum Solanum tuberosum Solanum villosum Sonchus oleraceus Soymida febrifuga Sphaeranthus amaranthoides Sphenoclea zeylanica Spiranthes australis Spiranthes sinensis Spondias pinnata Stellaria media Stellera chamaejasme Stephania japonica Sterculia alata Sterculia foetida Sterculia villosa Stereospermum tetragonum Stevia rebaudiana Striga asiatica Strophanthus boivinii Strychnos minor Strychnos nux-vomica Strychnos potatorum Suaeda maritima Suregada multiflora Swertia angustifolia Swertia bimaculata Swertia cordata Swertia paniculata Swietenia macrophylla Swietenia mahagoni Syzygium alternifolium Syzygium aromaticum Syzygium cumini Syzygium jambos Syzygium samarangense Tabebuia aurea Tabebuia avellanedae Talinum portulacifolium Tamarindus indica Taxus baccata Tecoma castanifolia Tephrosia calophylla Tephrosia purpurea Teramnus labialis Terminalia alata Terminalia catappa Terminalia chebula Terminalia elliptica Terminalia pallida Teucrium botrys Teucrium royleanum Thalictrum foliolosum Thespesia populnea Thunbergia erecta Thunbergia fragrans Thunbergia grandiflora Thymus linearis Tiliacora acuminata Tiliacora racemosa Tinospora cordifolia Tinospora crispa Tinospora sinensis Toona ciliata Trewia nudiflora Tribulus terrestris Trichodesma indicum Trichosanthes cucumerina Trichosanthes palmata Trichosanthes tricuspidata Trifolium repens Trigonella foenum-graecum Triumfetta rhomboidea Tylophora indica Uraria picta Urena lobata Urena sinuata Urginea coromandeliana Vachellia horrida Valeriana jatamansi Vanda tessellata Veronica serpyllifolia Viburnum coriaceum Vicia bakeri Vicia faba Vicia sativa Vigna radiata Vigna unguiculata Vinca rosea Viola rupestris Viscum album Vitex negundo Vitis vinifera Withania somnifera Wrightia tinctoria Wulfeniosis amherstiana Zamia furfuracea Ziziphus jujuba Ziziphus mauritiana
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