Search for Natural Products Related to Regeneration of the Neuronal Network

Physical basis of cognitive alterations in alzheimer's disease: Synapse loss is the major correlate of cognitive impairment

Terry, R. D., Masliah, E., Salmon, D. P., Butters, N., DeTeresa, R., Hill, R., Hansen, L. A., & Katzman, R. (1991) · Annals of Neurology · doi:10.1002/ana.410300410 · Cited by 4,397

Alzheimer-type neuropathology in transgenic mice overexpressing V717F β-amyloid precursor protein

Games, D., Adams, D., Alessandrini, R., Barbour, R., Borthelette, P., Blackwell, C., Carr, T., Clemens, J., Donaldson, T., Gillespie, F., et al. (1995) · Nature · doi:10.1038/373523a0 · Cited by 2,516

Synapse loss in frontal cortex biopsies in Alzheimer's disease: Correlation with cognitive severity

DeKosky, S. T., & Scheff, S. W. (1990) · Annals of Neurology · doi:10.1002/ana.410270502 · Cited by 2,376

Amyloid β protein forms ion channels: implications for Alzheimer's disease pathophysiology

LIN, H., Bhatia, R., & Lal, R. (2001) · The FASEB Journal · doi:10.1096/fj.01-0377com · Cited by 656

DEGRADATION OF GINSENOSIDES IN HUMANS AFTER ORAL ADMINISTRATION

Tawab, M. A., Bahr, U., Karas, M., Wurglics, M., & Schubert‐Zsilavecz, M. (2003) · Drug Metabolism and Disposition · doi:10.1124/dmd.31.8.1065 · Cited by 440

Neuritic regeneration and synaptic reconstruction induced by withanolide A

Kuboyama, T., Tohda, C., & Komatsu, K. (2005) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706122 · Cited by 339

The morphological phenotype of β-amyloid plaques and associated neuritic changes in Alzheimer’s disease

Dickson, T. C., & Vickers, J. C. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00169-5 · Cited by 294

Peroxynitrite Mediates Neurotoxicity of Amyloid β-Peptide 1–42 - and Lipopolysaccharide-Activated Microglia

Xie, Z., Wei, M., Morgan, T. E., Fabrizio, P., Han, D., Finch, C. E., & Longo, V. D. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-09-03484.2002 · Cited by 272

β-Amyloid Fragment 25–35 Causes Mitochondrial Dysfunction in Primary Cortical Neurons

Casley, C. S., Land, J. M., Sharpe, M. A., Clark, J. B., Duchen, M. R., & Canevari, L. (2002) · Neurobiology of Disease · doi:10.1006/nbdi.2002.0516 · Cited by 207

Steroidal Lactones from Withania somnifera, an Ancient Plant for Novel Medicine

Mirjalili, M. H., Moyano, E., Bonfill, M., Cusido, R. M., & Palazón, J. (2009) · Molecules · doi:10.3390/molecules14072373 · Cited by 657

Coffee and its Consumption: Benefits and Risks

Butt, M. S., & Sultan, M. T. (2011) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408390903586412 · Cited by 631

Coffee: Biochemistry and Potential Impact on Health

Ludwig, I. A., Clifford, M. N., Lean, M. E. J., Ashihara, H., & Crozier, A. (2014) · Food Funct. · doi:10.1039/c4fo00042k · Cited by 537

Withania somnifera: an Indian ginseng

Kulkarni, S. K., & Dhir, A. (2008) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2007.09.011 · Cited by 416

Trigonelline: A Plant Alkaloid with Therapeutic Potential for Diabetes and Central Nervous System Disease

Zhou, J., Chan, L., & Zhou, S. (2012) · Current Medicinal Chemistry · doi:10.2174/092986712801323171 · Cited by 395

Coffee Constituents

Farah, A. (2012) · Coffee · doi:10.1002/9781119949893.ch2 · Cited by 330

Plants traditionally used in age related brain disorders—A survey of ethnobotanical literature

Adams, M. A., Gmünder, F., & Hamburger, M. O. (2007) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2007.07.016 · Cited by 328

Neuroprotective Effects of Coffee Bioactive Compounds: A Review

Socała, K., Szopa, A., Serefko, A., Poleszak, E., & Właź, P. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms22010107 · Cited by 271

Panax Ginseng Enhances Cognitive Performance in Alzheimer Disease

Lee, S., Chu, K., Sim, J.-Y., Heo, J., & Kim, M. (2008) · Alzheimer Disease & Associated Disorders · doi:10.1097/wad.0b013e31816c92e6 · Cited by 244

Neuroprotective Herbs for the Management of Alzheimer’s Disease

Gregory, J., Vengalasetti, Y. V., Bredesen, D. E., & Rao, R. V. (2021) · Biomolecules · doi:10.3390/biom11040543 · Cited by 264

Ayurvedic medicinal plants for Alzheimer’s disease: A review

Rao, R. V., Descamps, O., John, V., & Bredesen, D. E. (2012) · Alzheimer's Research & Therapy · doi:10.1186/alzrt125 · Cited by 213

Multi-Target-Directed Ligands and other Therapeutic Strategies in the Search of a Real Solution for Alzheimer’s Disease

Agis-Torres, A., Sollhuber, M., Fernandez, M., & Sanchez-Montero, J. M. (2014) · Current Neuropharmacology · doi:10.2174/1570159x113116660047 · Cited by 202

Fast simultaneous analysis of caffeine, trigonelline, nicotinic acid and sucrose in coffee by liquid chromatography–mass spectrometry

Perrone, D., Donangelo, C. M., & Farah, A. (2008) · Food Chemistry · doi:10.1016/j.foodchem.2008.03.012 · Cited by 190

The Role of Phytochemicals in the Treatment and Prevention of Dementia

Howes, M. R., & Perry, E. K. (2011) · Drugs & Aging · doi:10.2165/11591310-000000000-00000 · Cited by 187

Withanoside IV and its active metabolite, sominone, attenuate Aβ(25–35)‐induced neurodegeneration

Kuboyama, T., Tohda, C., & Komatsu, K. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04664.x · Cited by 171

Diosgenin is an exogenous activator of 1,25D3-MARRS/Pdia3/ERp57 and improves Alzheimer's disease pathologies in 5XFAD mice

Tohda, C., Urano, T., Umezaki, M., Nemere, I., & Kuboyama, T. (2012) · Scientific Reports · doi:10.1038/srep00535 · Cited by 170

Medicinal Plants and Dementia Therapy: Herbal Hopes for Brain Aging?

Perry, E. K., & Howes, M. R. (2010) · CNS Neuroscience & Therapeutics · doi:10.1111/j.1755-5949.2010.00202.x · Cited by 160

Reductions in levels of the Alzheimer's amyloid β peptide after oral administration of ginsenosides

Chen, F., Eckman, E. A., & Eckman, C. B. (2006) · The FASEB Journal · doi:10.1096/fj.05-5530fje · Cited by 160

Withania somnifera root extract improves catecholamines and physiological abnormalities seen in a Parkinson's disease model mouse

Rajasankar, S., Manivasagam, T., Venkatachalam, S., Prakash, S., Muthusamy, R., Krishnamurti, A., & Surendran, S. (2009) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2009.08.003 · Cited by 161

Analysis of withanolides in root and leaf of Withania somnifera by HPLC with photodiode array and evaporative light scattering detection

Chaurasiya, N. D., Uniyal, G. C., Lal, P., Misra, L., Sangwan, R. S., Tuli, R., & Sangwan, R. S. (2007) · Phytochemical Analysis · doi:10.1002/pca.1029 · Cited by 146

Establishment of cell suspension cultures of Withania somnifera for the production of withanolide A

Nagella, P., & Murthy, H. N. (2010) · Bioresource Technology · doi:10.1016/j.biortech.2010.03.078 · Cited by 143

Ashwagandha leaf extract: A potential agent in treating oxidative damage and physiological abnormalities seen in a mouse model of Parkinson's disease

Rajasankar, S., Manivasagam, T., & Surendran, S. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.02.044 · Cited by 140

Flavors of the future: Health benefits of flavor precursors and volatile compounds in plant foods

Ayseli, M. T., & Ayseli, Y. I. (2015) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2015.11.005 · Cited by 138

Neuroprotective role of Withania somnifera root extract in maneb-paraquat induced mouse model of parkinsonism

Prakash, J., Yadav, S. K., Chouhan, S., & Singh, S. P. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1005-4 · Cited by 128

Neurotrophic Natural Products: Chemistry and Biology

Xu, J., Lacoske, M. H., & Theodorakis, E. A. (2013) · Angewandte Chemie International Edition · doi:10.1002/anie.201302268 · Cited by 124

A Review on Biosynthesis, Analytical Techniques, and Pharmacological Activities of Trigonelline as a Plant Alkaloid

Mohamadi, N., Sharififar, F., Pournamdari, M., & Ansari, M. (2017) · Journal of Dietary Supplements · doi:10.1080/19390211.2017.1329244 · Cited by 126

Withanolide A Biogeneration in in Vitro Shoot Cultures of Ashwagandha (Withania somnifera DUNAL), a Main Medicinal Plant in Ayurveda

Sangwan, R. S., Chaurasiya, N. D., Lal, P., Misra, L., Uniyal, G. C., Tuli, R., & Sangwan, R. S. (2007) · Chemical and Pharmaceutical Bulletin · doi:10.1248/cpb.55.1371 · Cited by 118

Trigonelline Is a Novel Phytoestrogen in Coffee Beans ,

Allred, K. F., Yackley, K. M., Vanamala, J. K. P., & Allred, C. D. (2009) · Journal of Nutrition · doi:10.3945/jn.109.108001 · Cited by 117

Promotion of axonal maturation and prevention of memory loss in mice by extracts of Astragalus mongholicus

Tohda, C., Tamura, T., Matsuyama, S., & Komatsu, K. (2006) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706865 · Cited by 116

Inhibition of the NEMO/IKKβ association complex formation, a novel mechanism associated with the NF-κB activation suppression by Withania somnifera’s key metabolite withaferin A

Grover, A., Shandilya, A., Punetha, A., Bisaria, V. S., & Sundar, D. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-s4-s25 · Cited by 113

Trigonelline and related nicotinic acid metabolites: occurrence, biosynthesis, taxonomic considerations, and their roles in planta and in human health

Ashihara, H., Ludwig, I. A., Katahira, R., Yokota, T., Fujimura, T., & Crozier, A. (2015) · Phytochemistry Reviews · doi:10.1007/s11101-014-9375-z · Cited by 110

Determination of withaferin A and withanolide A in mice plasma using high-performance liquid chromatography-tandem mass spectrometry: Application to pharmacokinetics after oral administration of Withania somnifera aqueous extract

Patil, D., Gautam, M., Mishra, S. K., Suresh, K., Gairola, S., Jadhav, S. S., Pawar, S., & Patwardhan, B. (2013) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2013.03.001 · Cited by 108

Acetylcholinesterase enzyme inhibitory potential of standardized extract of Trigonella foenum graecum L and its constituents

Satheeshkumar, N., Mukherjee, P. K., Bhadra, S., & Saha, B. P. (2009) · Phytomedicine · doi:10.1016/j.phymed.2009.06.006 · Cited by 107

Pyridine alkaloids with activity in the central nervous system

Lin, S. X., Curtis, M. A., & Sperry, J. (2020) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2020.115820 · Cited by 106

Neuroprotective effects of Astragaloside IV in 6-hydroxydopamine-treated primary nigral cell culture

Chan, W. S., Durairajan, S. S. K., Lu, J., Wang, Y., Xie, L., Kum, W.-F., Koo, I., Yung, K. K. L., & Li, M. (2009) · Neurochemistry International · doi:10.1016/j.neuint.2009.04.012 · Cited by 107

W ithania somnifera (Ashwagandha) in neurobehavioural disorders induced by brain oxidative stress in rodents: a systematic review and meta-analysis

Durg, S., Dhadde, S. B., Vandal, R., Shivakumar, B. S., & Charan, C. S. (2015) · Journal of Pharmacy and Pharmacology · doi:10.1111/jphp.12398 · Cited by 110

A Decade of Molecular Understanding of Withanolide Biosynthesis and In vitro Studies in Withania somnifera (L.) Dunal: Prospects and Perspectives for Pathway Engineering

Dhar, N., Razdan, S., Rana, S., Bhat, W. W., Vishwakarma, R. A., & Lattoo, S. K. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.01031 · Cited by 105

Withanolides and Related Steroids

Misico, R. I., Nicotra, V. E., Oberti, J. C., Barboza, G. E., Gil, R. R., & Burton, G. (2011) · Fortschritte der Chemie Organischer Naturstoffe/Fortschritte der Chemie organischer Naturstoffe/Progress in the chemistry of organic natural products · doi:10.1007/978-3-7091-0748-5_3 · Cited by 99

Selective killing of cancer cells by leaf extract of Ashwagandha: Components, activity and pathway analyses

Widodo, N., Takagi, Y., Shrestha, B. G., Ishii, T., Kaul, S. C., & Wadhwa, R. (2008) · Cancer Letters · doi:10.1016/j.canlet.2007.11.037 · Cited by 96

Water Extract of Ashwagandha Leaves Has Anticancer Activity: Identification of an Active Component and Its Mechanism of Action

Wadhwa, R., Singh, R., Gao, R., Shah, N., Widodo, N., Nakamoto, T., Ishida, Y., Terao, K., & Kaul, S. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077189 · Cited by 90

The Role of Bioactive Compounds on the Promotion of Neurite Outgrowth

More, S. V., Koppula, S., Kim, I., Kumar, H., Kim, B.-W., & Choi, D. (2012) · Molecules · doi:10.3390/molecules17066728 · Cited by 89

Risk Assessment of Trigonelline in Coffee and Coffee By-Products

Konstantinidis, N., Franke, H., Schwarz, S., & Lachenmeier, D. W. (2023) · Molecules · doi:10.3390/molecules28083460 · Cited by 94

A Unified Approach for the Stereoselective Total Synthesis of Pyridone Alkaloids and Their Neuritogenic Activity

Jessen, H. J., Schumacher, A., Shaw, T. W., Pfaltz, A., & Gademann, K. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201007671 · Cited by 87

A Potential Alternative against Neurodegenerative Diseases: Phytodrugs

Pérez‐Hernández, J., Zaldívar-Machorro, V. J., David, V.-P., Vega‐Avila, E., & Chavarría, A. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/8378613 · Cited by 88

Anti-neuroinflammation effect of ginsenoside Rbl in a rat model of Alzheimer disease

Wang, Y., Liu, J., Zhang, Z., Bi, P., Qi, Z., & Zhang, C. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.09.076 · Cited by 87

Hsp90/Cdc37 Chaperone/co-chaperone complex, a novel junction anticancer target elucidated by the mode of action of herbal drug Withaferin A

Grover, A., Shandilya, A., Agrawal, V., Pratik, P., Bhasme, D., Bisaria, V. S., & Sundar, D. (2011) · BMC Bioinformatics · doi:10.1186/1471-2105-12-s1-s30 · Cited by 85

Trigonelline mitigates lipopolysaccharide-induced learning and memory impairment in the rat due to its anti-oxidative and anti-inflammatory effect

Khalili, M., Alavi, M., Esmaeil-Jamaat, E., Baluchnejadmojarad, T., & Roghani, M. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.06.019 · Cited by 83

Effects of macroelements and nitrogen source on biomass accumulation and withanolide-A production from cell suspension cultures of Withania somnifera (L.) Dunal

Nagella, P., & Murthy, H. N. (2010) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-010-9799-0 · Cited by 82

Total Synthesis of Cyrneine A

Elamparuthi, E., Fellay, C., Neuburger, M. A., & Gademann, K. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201200515 · Cited by 80

Effect of processing on bioaccessibility and bioavailability of bioactive compounds in coffee beans

Wu, H., Gu, J., Amrit, B. K., Nawaz, M. A., Barrow, C. J., Dunshea, F. R., & Suleria, H. A. R. (2021) · Food Bioscience · doi:10.1016/j.fbio.2021.101373 · Cited by 85

Water extract from the leaves of Withania somnifera protect RA differentiated C6 and IMR-32 cells against glutamate-induced excitotoxicity

Kataria, H., Wadhwa, R., Kaul, S. C., & Kaur, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037080 · Cited by 77

In vitro plant regeneration from cotyledonary nodes of Withania somnifera (L.) Dunal and assessment of clonal fidelity using RAPD and ISSR markers

Nayak, S., Kumar, S., Satapathy, K. B., Moharana, A., Behera, B., Barık, D. P., Acharya, L., Mohapatra, P. K., Jena, P. K., & Naik, S. K. (2012) · Acta Physiologiae Plantarum · doi:10.1007/s11738-012-1063-2 · Cited by 77

Ginsenoside Rg3 promotes beta-amyloid peptide degradation by enhancing gene expression of neprilysin

Yang, L., Hao, J., Zhang, J., Xia, W., Dong, X., Hu, X., Kong, F., & Cui, X. (2009) · Journal of Pharmacy and Pharmacology · doi:10.1211/jpp.61.03.0013 · Cited by 75

Protective effects of trigonelline against indomethacin-induced gastric ulcer in rats and potential underlying mechanisms

Antonisamy, P., Arasu, M. V., Dhanasekaran, M., Choi, K. C., Aravinthan, A., Kim, N. S., Kang, C. W., & Kim, J. (2015) · Food & Function · doi:10.1039/c5fo00403a · Cited by 74

Rhizospheric biological weapons for growth enhancement and Meloidogyne incognita management in Withania somnifera cv. Poshita

Saikia, S. K., Tiwari, S., & Pandey, R. (2013) · Biological Control · doi:10.1016/j.biocontrol.2013.01.014 · Cited by 74

Trigonelline insulates against oxidative stress, proinflammatory cytokines and restores BDNF levels in lipopolysaccharide induced cognitive impairment in adult mice

Chowdhury, A. A., Gawali, N. B., Munshi, R., & Juvekar, A. R. (2017) · Metabolic Brain Disease · doi:10.1007/s11011-017-0147-5 · Cited by 76

Green tea catechins potentiate the neuritogenic action of brain-derived neurotrophic factor: Role of 67-kDa laminin receptor and hydrogen peroxide

Gundimeda, U., McNeill, T. H., Fan, T., Deng, R., Rayudu, D. V., Chen, Z., Cadenas, E., & Gopalakrishna, R. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.01.166 · Cited by 70

Trigonelline protects hippocampus against intracerebral Aβ(1–40) as a model of Alzheimer’s disease in the rat: insights into underlying mechanisms

Fahanik‐Babaei, J., Baluchnejadmojarad, T., Nikbakht, F., & Roghani, M. (2018) · Metabolic Brain Disease · doi:10.1007/s11011-018-0338-8 · Cited by 76

Green tea polyphenols potentiate the action of nerve growth factor to induce neuritogenesis: Possible role of reactive oxygen species

Gundimeda, U., McNeill, T. H., Schiffman, J. E., Hinton, D. R., & Gopalakrishna, R. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22519 · Cited by 65

Simultaneous Determination of Alkaloids in Green Coffee Beans from Ethiopia: Chemometric Evaluation of Geographical Origin

Mehari, B., Redi‐Abshiro, M., Chandravanshi, B. S., Atlabachew, M., Combrinck, S., & McCrindle, R. I. (2015) · Food Analytical Methods · doi:10.1007/s12161-015-0340-2 · Cited by 64

Potential nutraceutical and food additive properties and risks of coffee: a comprehensive overview

Saeed, M., Naveed, M., Bibi, J., Kamboh, A. A., Phil, L., & Sun, C. (2019) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2018.1489368 · Cited by 68

Mechanisms of action of coffee bioactive compounds – a key to unveil the coffee paradox

Machado, F. D. S., Coimbra, M. A., del Castillo, M. D., & Coreta-Gomes, F. M. (2023) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2023.2221734 · Cited by 69

Unique Medicinal Properties of Withania somnifera: Phytochemical Constituents and Protein Component

Dar, P. A., Singh, L. R., Kamal, M. A., & Dar, T. A. (2016) · Current Pharmaceutical Design · doi:10.2174/1381612822666151125001751 · Cited by 61

Withanolides: Phytoconstituents with significant pharmacological activities

Singh, A., Duggal, S., Singh, H., Singh, J., & Katekhaye, S. D. (2010) · International Journal of Green Pharmacy · doi:10.4103/0973-8258.74130 · Cited by 59

Pharmacological exploration of traditional plants for the treatment of neurodegenerative disorders

Wahid, M., Ali, A., Saqib, F., Aleem, A., Bibi, S., Afzal, K., Ali, A., Baig, A., Khan, S. A., & Asad, M. H. H. B. (2020) · Phytotherapy Research · doi:10.1002/ptr.6742 · Cited by 61

Synthesis of Withanolide A, Biological Evaluation of Its Neuritogenic Properties, and Studies on Secretase Inhibition

Jana, C. K., Hoecker, J., Woods, T. M., Jessen, H. J., Neuburger, M. A., & Gademann, K. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201101869 · Cited by 57

Recent advances in elucidating the biological properties of Withania somnifera and its potential role in health benefits

Alam, N., Hossain, M., Khalil, M. I., Moniruzzaman, M., Sulaiman, S. A., & Gan, S. H. (2011) · Phytochemistry Reviews · doi:10.1007/s11101-011-9221-5 · Cited by 55

Trigonelline recovers memory function in Alzheimer’s disease model mice: evidence of brain penetration and target molecule

Farid, M. M., Yang, X., Kuboyama, T., & Tohda, C. (2020) · Scientific Reports · doi:10.1038/s41598-020-73514-1 · Cited by 56

Total Synthesis of Gelsemiol

Burch, P., Binaghi, M., Scherer, M., Wentzel, C., Bossert, D., Eberhardt, L., Neuburger, M. A., Scheiffele, P., & Gademann, K. (2013) · Chemistry - A European Journal · doi:10.1002/chem.201203746 · Cited by 55

Bringing natural products into the fold – exploring the therapeutic lead potential of secondary metabolites for the treatment of protein-misfolding-related neurodegenerative diseases

Joyner, P. M., & Cichewicz, R. H. (2010) · Natural Product Reports · doi:10.1039/c0np00017e · Cited by 54

Exploring plant tissue culture inWithania somnifera(L.) Dunal:in vitropropagation and secondary metabolite production

Shasmita, Manoj, K., & Naik, S. K. (2017) · Critical Reviews in Biotechnology · doi:10.1080/07388551.2017.1416453 · Cited by 52

Protection of Trigonelline on Experimental Diabetic Peripheral Neuropathy

Zhou, J., & Zhou, S.-W. (2012) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2012/164219 · Cited by 51

Biotechnological interventions inWithania somnifera(L.) Dunal

Singh, P., Guleri, R., Singh, V., Kaur, G., Kataria, H., Singh, B. B., Kaur, G., Kaul, S. C., Wadhwa, R., & Pati, P. K. (2015) · Biotechnology and Genetic Engineering Reviews · doi:10.1080/02648725.2015.1020467 · Cited by 51

Direct Pd(II)-Catalyzed Site-Selective C5-Arylation of 2-Pyridone Using Aryl Iodides

Maity, S., Das, D., Sarkar, S., & Samanta, R. (2018) · Organic Letters · doi:10.1021/acs.orglett.8b02112 · Cited by 50

A compound herbal preparation (CHP) in the treatment of children with adhd: A randomized controlled trial

Katz, M., Adar Levine, A., Kol-Degani, H., & Kav-Venaki, L. (2010) · Journal of Attention Disorders · doi:10.1177/1087054709356388 · Cited by 48

Treatment with ginseng total saponins improves the neurorestoration of rat after traumatic brain injury

Hu, B., Liu, X., Qiang, R., Jiang, Z., Xu, L., Wang, G., Li, X., & Peng, B. (2014) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2014.07.009 · Cited by 48

Inhibitory Effects of Eleutherococcus senticosus Extracts on Amyloid β(25-35)–Induced Neuritic Atrophy and Synaptic Loss

Tohda, C., Ichimura, M., Bai, Y., Tanaka, K., Zhu, S., & Komatsu, K. (2008) · Journal of Pharmacological Sciences · doi:10.1254/jphs.08046fp · Cited by 48

Morphology and withanolide production of Withania coagulans hairy root cultures

Mirjalili, H. M., Fakhr-Tabatabaei, S. M., Bonfill, M., Alizadeh, H., Cusido, R. M., Ghassempour, A., & Palazón, J. (2009) · Engineering in Life Sciences · doi:10.1002/elsc.200800081 · Cited by 47

Effect of Withania somnifera Supplementation on Rotenone-Induced Oxidative Damage in Cerebellum and Striatum of the Male Mice Brain

Manjunath, M. J., & ., M. (2013) · Central Nervous System Agents in Medicinal Chemistry · doi:10.2174/1871524911313010007 · Cited by 45

Toxic Chemical Compounds of the Solanaceae

Pomilio, A. B., Falzoni, E., & Vitale, A. A. (2008) · Natural Product Communications · doi:10.1177/1934578x0800300420 · Cited by 45

Trigonelline Ameliorates Oxidative Stress in Type 2 Diabetic Goto-Kakizaki Rats

Yoshinari, O., Takenake, A., & Igarashi, K. (2012) · Journal of Medicinal Food · doi:10.1089/jmf.2012.2311 · Cited by 44

Withania somnifera Prevents Morphine Withdrawal-Induced Decrease in Spine Density in Nucleus Accumbens Shell of Rats: A Confocal Laser Scanning Microscopy Study

Kasture, S. B., Vinci, S., Ibba, F., Puddu, A., Marongiu, M., Balasubramanian, M., Pisanu, A., Lecca, D., Zernig, G., & Acquas, E. (2009) · Neurotoxicity Research · doi:10.1007/s12640-009-9069-2 · Cited by 44

Emodin induces neurite outgrowth through PI3K/Akt/GSK-3β-mediated signaling pathways in Neuro2a cells

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