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

Clinical Efficacy of Manasamitra Vataka (an Ayurveda Medication) on Generalized Anxiety Disorder with Comorbid Generalized Social Phobia: A Randomized Controlled Study

Tubaki, B. R., Chandrashekar, C. R., Sudhakar, D., Prabha, T. N. S., Lavekar, G. S., & Kutty, B. M. (2012) · The Journal of Alternative and Complementary Medicine · doi:10.1089/acm.2010.0778 · Cited by 40

Total Synthesis and Neuritotrophic Activity of Farinosone C and Derivatives

Jessen, H. J., Barbaras, D., Hamburger, M. O., & Gademann, K. (2009) · Organic Letters · doi:10.1021/ol901277q · Cited by 34

Neurobehavioral assessment of hydroalcoholic extract ofTrigonella foenum-graecumseeds in rodent models of Parkinson’s disease

Gaur, V., Bodhankar, S. L., Mohan, V., & Thakurdesai, P. A. (2013) · Pharmaceutical Biology · doi:10.3109/13880209.2012.747547 · Cited by 34

Oil palm phenolics confer neuroprotective effects involving cognitive and motor functions in mice

Leow, S.-S., Sekaran, S. D., Tan, Y., Sundram, K., & Sambanthamurthi, R. (2013) · Nutritional Neuroscience · doi:10.1179/1476830512y.0000000047 · Cited by 35

Ein einheitlicher Ansatz zur stereoselektiven Totalsynthese von Pyridonalkaloiden und deren neuritogene Aktivität

Jessen, H. J., Schumacher, A., Shaw, T. W., Pfaltz, A., & Gademann, K. (2011) · Angewandte Chemie · doi:10.1002/ange.201007671 · Cited by 33

Natural Alkaloid Compounds as Inhibitors for Alpha-Synuclein Seeded Fibril Formation and Toxicity

Ghanem, S. S., Fayed, H. S., Zhu, Q., Lu, J., Vaikath, N. N., Ponraj, J., Mansour, S. A., & El‐Agnaf, O. M. A. (2021) · Molecules · doi:10.3390/molecules26123736 · Cited by 33

Association Constants of Pyridine and Piperidine Alkaloids to Amyloid ß Peptide Determined by Electrochemical Impedance Spectroscopy

Grabowska, I., Radecka, H., Burza, A., Radecki, J., Kaliszan, M., & Kaliszan, R. (2010) · Current Alzheimer Research · doi:10.2174/156720510790691290 · Cited by 32

Propensity of Withania somnifera to Attenuate Behavioural, Biochemical, and Histological Alterations in Experimental Model of Stroke

Sood, A., Kumar, A., Dhawan, D., & Sandhir, R. (2015) · Cellular and molecular neurobiology · doi:10.1007/s10571-015-0305-4 · Cited by 29

Impaired motor learning attributed to altered AMPA receptor function in the cerebellum of rats with temporal lobe epilepsy: Ameliorating effects of Withania somnifera and withanolide A

Soman, S. K., Anju, T. R., Jayanarayanan, S., Antony, S., & Paulose, C. S. (2013) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2013.01.007 · Cited by 31

Risk Assessment of Coffee Cherry (Cascara) Fruit Products for Flour Replacement and Other Alternative Food Uses

Eckhardt, S., Franke, H., Schwarz, S., & Lachenmeier, D. W. (2022) · Molecules · doi:10.3390/molecules27238435 · Cited by 39

The Multifaceted Role of Neuroprotective Plants in Alzheimer’s Disease Treatment

Zieneldien, T., Kim, J., & Cao, C. (2022) · Geriatrics · doi:10.3390/geriatrics7020024 · Cited by 29

The regenerative potential of honey: a comprehensive literature review

Iftikhar, A., Nausheen, R., Mukhtar, I., Iqbal, R. K., Raza, A., Yasin, A., & Anwar, H. (2022) · Journal of Apicultural Research · doi:10.1080/00218839.2022.2028969 · Cited by 29

Kinetics and molecular docking of vasicine from Adhatoda vasica : An acetylcholinesterase inhibitor for Alzheimer's disease

Ali, S. K., Hamed, A. R., Soltan, M. M., Halawany, A. M. E., Hegazy, U. M., & Hussein, A. A. (2016) · South African Journal of Botany · doi:10.1016/j.sajb.2015.09.021 · Cited by 30

Substituent-controlled chemoselective synthesis of multi-substituted pyridones via a one-pot three-component cascade reaction

Liu, S., Li, J., Lin, J.-J., Liu, F., Liu, T., & Huang, C. (2020) · Organic & Biomolecular Chemistry · doi:10.1039/c9ob02456e · Cited by 29

High-Dosage Pyridoxine-Induced Auditory Neuropathy and Protection with Coffee in Mice

Hong, B. N., Yi, T., Kim, S. Y., & Kang, T. H. (2009) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.32.597 · Cited by 27

Direct shoot organogenesis from petiole and leaf discs of Withania somnifera (L.) Dunal

Bimal, K. G., Eun, S. S., Eun, H. K., Kabir, L., Chang, Y. Y., & Ill, M. C. (2010) · AFRICAN JOURNAL OF BIOTECHNOLOGY · doi:10.5897/ajb10.1250 · Cited by 27

Truncated militarinone fragments identified by total chemical synthesis induce neurite outgrowth

Schmid, F., Jessen, H. J., Burch, P., & Gademann, K. (2012) · MedChemComm · doi:10.1039/c2md20181j · Cited by 26

Facilitating effects of Buyang Huanwu decoction on axonal regeneration after peripheral nerve transection

Kim, K. J., & Namgung, U. (2017) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2017.10.036 · Cited by 26

Effect of Light Quality on Metabolomic, Ionomic, and Transcriptomic Profiles in Tomato Fruit

Xiao, L., Shibuya, T., Watanabe, T., Kato, K., & Kanayama, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113288 · Cited by 25

An overview of biotechnological interventions and abiotic elicitors on biomass and withanolide biosynthesis in Withania somnifera (L.) Dunal

Sharma, L., Maurya, B., & Rai, S. P. (2023) · Industrial Crops and Products · doi:10.1016/j.indcrop.2023.116238 · Cited by 24

Dynamic Metabolic Regulation by a Chromosome Segment from a Wild Relative During Fruit Development in a Tomato Introgression Line, IL8-3

Ikeda, H., Shibuya, T., Imanishi, S., Aso, H., Nishiyama, M., & Kanayama, Y. (2016) · Plant and Cell Physiology · doi:10.1093/pcp/pcw075 · Cited by 24

The potential therapeutic role of Fenugreek saponin against Alzheimer's disease: Evaluation of apoptotic and acetylcholinesterase inhibitory activities

Khalil, W. K. B., Roshdy, H. M., & Kassem, S. M. (2016) · Journal of Applied Pharmaceutical Science · doi:10.7324/japs.2016.60925 · Cited by 23

An Insight in Pathophysiological Mechanism of Alzheimer's Disease and its Management Using Plant Natural Products

Firdaus, Z., & Singh, T. D. (2020) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557520666200730155928 · Cited by 23

Withania somnifera root powder protects againist post-traumatic stress disorder-induced memory impairment

Alzoubi, K. H., Hilo, A. S. A., Al-Balas, Q. A., El‐Salem, K., El‐Elimat, T., & Alali, F. Q. (2019) · Molecular Biology Reports · doi:10.1007/s11033-019-04915-3 · Cited by 22

Metal-free regioselective direct thiolation of 2-pyridones

Phakdeeyothin, K., & Yotphan, S. (2019) · Organic & Biomolecular Chemistry · doi:10.1039/c9ob01061k · Cited by 21

Plant Biochemistry

Ashihara, H. (2014) · Coffee in Health and Disease Prevention · doi:10.1016/b978-0-12-409517-5.00003-6 · Cited by 21

Functionally Optimized Neuritogenic Farinosone C Analogs: SAR-Study and Investigations on Their Mode of Action

Burch, P., Chicca, A., Gertsch, J., & Gademann, K. (2013) · ACS Medicinal Chemistry Letters · doi:10.1021/ml400435h · Cited by 21

Profiling withanolide A for therapeutic targets in neurodegenerative diseases

Crane, E. A., Heydenreuter, W., Beck, K. R., Strajhar, P., Vomacka, J., Smieško, M., Mons, E., Barth, L., Neuburger, M. A., Vedani, A., et al. (2019) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2019.03.022 · Cited by 20

Totalsynthese von Cyrnein A

Elamparuthi, E., Fellay, C., Neuburger, M. A., & Gademann, K. (2012) · Angewandte Chemie · doi:10.1002/ange.201200515 · Cited by 19

Neurite Outgrowth on Nanocomposite Scaffolds Synthesized from PLGA and Carboxylated Carbon Nanotubes

Lee, H. J., Yoon, O. J., Kim, D. H., Jang, Y. M., Kim, H. W., Lee, W. B., Lee, N., & Kim, S. S. (2009) · Advanced Engineering Materials · doi:10.1002/adem.200900144 · Cited by 19

An in silico guided identification of nAChR agonists from Withania somnifera

Remya, C., Dileep, K., Variayr, E. J., & Sadasivan, C. (2016) · Frontiers in Life Science · doi:10.1080/21553769.2016.1207569 · Cited by 20

Quantifying orientational regeneration of injured neurons by natural product concentration gradients in a 3D microfluidic device

Tang, Y., Qiu, Q., Zhang, F., Xie, M., & Huang, W. (2018) · Lab on a Chip · doi:10.1039/c7lc01143a · Cited by 18

A directing group free Pd( ii )-catalysed desulfitative C6-arylation of 2-pyridone using an arylsulfonyl chloride

Karmakar, U., & Samanta, R. (2020) · Organic & Biomolecular Chemistry · doi:10.1039/d0ob01716g · Cited by 19

Correction: 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/annotation/b7059f27-5970-4734-8601-9913adcce984 · Cited by 19

Literature-Related Discovery (LRD)

Kostoff, R. N., Block, J. A., Solka, J. L., Briggs, M. B., Rushenberg, R. L., Stump, J. A., Johnson, D., Lyons, T. J., & Wyatt, J. R. (2007) · Defense Technical Information Center (DTIC) · doi:10.21236/ada473438 · Cited by 19

The antibiotic doxycycline mimics the NGF signaling in PC12 cells: A relevant mechanism for neuroprotection

Amaral, L. D., Santos, N. A. G. D., Sisti, F. M., Del Bel, E., & Santos, A. C. D. (2021) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2021.109454 · Cited by 18

Neurotrophe Naturstoffe – ihre Chemie und Biologie

Xu, J., Lacoske, M. H., & Theodorakis, E. A. (2013) · Angewandte Chemie · doi:10.1002/ange.201302268 · Cited by 18

Distribution and phytomedicinal aspects of Paris polyphylla Smith from the Eastern Himalayan Region: A review

Sharma, A., Kalita, P., & Tag, H. (2015) · TANG [HUMANITAS MEDICINE] · doi:10.5667/tang.2015.0001 · Cited by 18

Insights into the Impact of a Membrane-Anchoring Moiety on the Biological Activities of Bivalent Compounds As Potential Neuroprotectants for Alzheimer’s Disease

Liu, H., Jiang, Y., Liu, K., Gómez‐Murcia, V., Ma, X., Torrecillas, A., Chen, Q., Zhu, X., Lesnefsky, E. J., Gómez-Fernández, J. C., et al. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b01284 · Cited by 18

Elucidating the Improvement in Vascular Endothelial Function from Sakurajima Daikon and Its Mechanism of Action: A Comparative Study with Raphanus sativus

Kuroda, R., Kazumura, K., Ushikata, M., Minami, Y., & Kajiya, K. (2018) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.8b01750 · Cited by 18

Quantitative determination of trigonelline in mouse serum by means of hydrophilic interaction liquid chromatography–MS/MS analysis: Application to a pharmacokinetic study

Szczesny, D., Bartosińska, E., Jacyna, J., Patejko, M., Siluk, D., & Kaliszan, R. (2017) · Biomedical Chromatography · doi:10.1002/bmc.4054 · Cited by 17

The Corey-Seebach Reagent in the 21st Century: A Review

Haroon, M., Zahoor, A. F., Ahmad, S., Mansha, A., Irfan, M., Mushtaq, A., Akhtar, R., Irfan, A., Kotwica-Mojzych, K., & Mojzych, M. (2023) · Molecules · doi:10.3390/molecules28114367 · Cited by 17

Chronic toxicity of crude ricinine in rats assessed by 1 H NMR metabolomics analysis

Guo, P., Wei, D., Wang, J., Dong, G., Zhang, Q., Yang, M., & Kong, L. (2015) · RSC Advances · doi:10.1039/c4ra14660c · Cited by 16

Enhanced axonal regeneration of the injured sciatic nerve by administration of Buyang Huanwu decoction

Chang, I. A., Lim, H. D., Kim, K. J., Shin, H., & Namgung, U. (2016) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2016.10.053 · Cited by 16

Echinocystic Acid Facilitates Neurite Outgrowth in Neuroblastoma Neuro2a Cells and Enhances Spatial Memory in Aged Mice

Park, H. J., Kwon, H., Lee, S., Jung, J. W., Ryu, J. H., Jang, D. S., Lee, Y. C., & Kim, D. H. (2017) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b17-00324 · Cited by 16

Supplementation of fenugreek with choline–docosahexaenoic acid attenuates menopause induced memory loss, BDNF and dendritic arborization in ovariectomized rats

Konuri, A., Bhat, K. M. R., Rai, K. S., Gourishetti, K., & Mallimoggala, Y. (2020) · Anatomical Science International · doi:10.1007/s12565-020-00574-8 · Cited by 17

Caesalpinia mimosoides Leaf Extract Promotes Neurite Outgrowth and Inhibits BACE1 Activity in Mutant APP-Overexpressing Neuronal Neuro2a Cells

Rangsinth, P., Duangjan, C., Sillapachaiyaporn, C., Isidoro, C., Prasansuklab, A., & Tencomnao, T. (2021) · Pharmaceuticals · doi:10.3390/ph14090901 · Cited by 16

Beneficial effect of diosgenin as a stimulator of NGF on the brain with neuronal damage induced by Aβ-42 accumulation and neurotoxicant injection

Koh, E.-K., Yun, W.-B., Kim, J.-E., Song, S., Sung, J.-E., Lee, H. A., Seo, E.-J., Jee, S. W., Bae, C.-J., & Hwang, D. Y. (2016) · Laboratory Animal Research · doi:10.5625/lar.2016.32.2.105 · Cited by 16

A comparative pharmacokinetics study of Ashwagandha (Withania somnifera) Root Extract sustained-release capsules: an open-label, randomized, two treatment, two-sequence, two period, single-dose crossover clinical study

Alluri, K. V., Thanawala, S., & Upadhyay, V. K. (2021) · International Journal of Basic & Clinical Pharmacology · doi:10.18203/2319-2003.ijbcp20214831 · Cited by 15

Green Coffee Bean

Garg, S. K. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802147-7.00047-4 · Cited by 17

Effect of Withania somnifera Dunal Root Extract on Behavioral Despair Model in Mice: a Possible Role for Nitric Oxide.

Attari, M., Jamaloo, F., Shadvar, S., Fakhraei, N., & Dehpour, A. R. (2016) · PubMed · Cited by 15

Human Wellbeing—Sociability, Performance, and Health

Folmer, B. M., Farah, A., Jones, L., & Fogliano, V. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803520-7.00020-7 · Cited by 15

Bioactive components of Chinese herbal medicine enhance endogenous neurogenesis in animal models of ischemic stroke

Li, J.-H., Chen, Z.-X., Zhang, X.-G., Li, Y., Yang, W.-T., Zheng, X.-W., Chen, S., Lu, L., Gu, Y., & Zheng, G. (2016) · Medicine · doi:10.1097/md.0000000000004904 · Cited by 15

GC MS Analysis of One Ayurvedic Preparation ‘Aswagandharishtam

Kotteswari, M., Rao, M. R. K., Kumar, S. A., Prabhu, K., Sundaram, R. L., & Dinakar, S. (2018) · Biomedical & Pharmacology Journal · doi:10.13005/bpj/1467 · Cited by 15

Synthese von Withanolid A, Untersuchung der neuritogenen Eigenschaften und Studien zur Sekretase‐Inhibierung

Jana, C. K., Hoecker, J., Woods, T. M., Jessen, H. J., Neuburger, M. A., & Gademann, K. (2011) · Angewandte Chemie · doi:10.1002/ange.201101869 · Cited by 14

Molecular mechanism of nur77 gene expression and downstream target genes in the early stage of forskolin-induced differentiation in PC12 cells

Maruoka, H., Yamazoe, R., Takahashi, R., Yatsuo, K., Ido, D., Fuchigami, Y., Hoshikawa, F., & Shimoke, K. (2020) · Scientific Reports · doi:10.1038/s41598-020-62968-y · Cited by 14

A Concise Review of Common Plant-derived Compounds as a Potential Therapy for Alzheimer's Disease and Parkinson's Disease: Insight into Structure-Activity-Relationship

Nishal, S., Phaugat, P., Bazaad, J., Dhaka, R., Khatkar, S., Khatkar, A., Khayatkashani, M., Alizadeh, P., Haghighi, S. M., Mehri, M., et al. (2022) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527321666220614110616 · Cited by 16

Coffee and its Active Compounds are Neuroprotective

Kim, J., & Lee, K. W. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-409517-5.00046-2 · Cited by 14

Protective effect of Habenaria intermedia tubers against acute and chronic physical and psychological stress paradigms in rats

Habbu, P., Smita, D. M., Mahadevan, K., Shastry, R., & Biradar, S. (2012) · Revista Brasileira de Farmacognosia · doi:10.1590/s0102-695x2012005000033 · Cited by 14

New Age Therapy for Alzheimer’s Disease by Neuronal Network Reconstruction

Tohda, C. (2016) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b16-00438 · Cited by 14

Ru( ii ) catalyzed chelation assisted C(sp 2 )–H bond functionalization along with concomitant (4 + 2) annulation

Sarkar, A., Saha, M., & Das, A. R. (2023) · Organic & Biomolecular Chemistry · doi:10.1039/d3ob00828b · Cited by 13

Alkaloids and Drug Discovery for Neurodegenerative Diseases

Howes, M. R. (2013) · Springer eBooks · doi:10.1007/978-3-642-22144-6_43 · Cited by 13

Plant Adaptogens: Natural Medicaments for 21 st Century?

Özdemir, Z., Bildziukevich, U., Wimmerová, M., Macůrková, A., Lovecká, P., & Wimmer, Z. (2018) · ChemistrySelect · doi:10.1002/slct.201702682 · Cited by 17

The Neurotrophic-Like Effect of Carvacrol: Perspective for Axonal and Synaptic Regeneration

Sisti, F., dos Santos, N. A. G., do Amaral, L., & dos Santos, A. C. (2021) · Neurotoxicity Research · doi:10.1007/s12640-021-00341-1 · Cited by 12

Caspase-1 and Cathepsin B Inhibitors from Marine Invertebrates, Aiming at a Reduction in Neuroinflammation

Moreno, R. I., Zambelli, V. O., Picolo, G., Cury, Y., Morandini, A. C., Marques, A. C., & Sciani, J. M. (2022) · Marine Drugs · doi:10.3390/md20100614 · Cited by 12

Acute physiological effects following Bacillus subtilis DE111 oral ingestion – a randomised, double blinded, placebo-controlled study

Colom, J., Freitas, D., Simon, A., Khokhlova, E. V., Mazhar, S., Buckley, M. J. M., Phipps, C., Deaton, J. G., Brodkorb, A., & Rea, K. (2023) · Beneficial Microbes · doi:10.3920/bm2022.0081 · Cited by 12

Natural products of relevance in the management of attention deficit hyperactivity disorder

Custódio, L. M. B., Vizetto‐Duarte, C., Cebeci, F., Özçelik, B., Sharopov, F. S., Gürer, E. S., Kumar, M., Iriti, M., Sharifi‐Rad, J., & Călina, D. C. (2022) · eFood · doi:10.1002/efd2.57 · Cited by 11

Green coffee as a novel agent for Alzheimer’s disease prevention by attenuating diabetes

Varghese, M., Ho, L., Wang, J., Zhao, W., Levine, S., Ono, K., Mannino, S., & Pasinetti, G. M. (2014) · Translational Neuroscience · doi:10.2478/s13380-014-0213-y · Cited by 12

Bogijetong decoction and its active herbal components protect the peripheral nerve from damage caused by taxol or nerve crush

Ahn, S. H., Chang, I. A., Kim, K. J., Kim, C.-J., Namgung, U., & Cho, C.-S. (2016) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-016-1391-7 · Cited by 11

Distal Axonal Proteins and Their Related MiRNAs in Cultured Cortical Neurons

Li, C., Zhang, Y., Levin, A. M., Fan, B. Y., Teng, H., Ghannam, M. M., Chopp, M., & Zhang, Z. G. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1266-7 · Cited by 10

Analysis of organic molecules, physicochemical parameters, and pollen as indicators for authenticity, botanical origin, type and quality of honey samples examined

Molina, O. F., Alizadeh, K., Bucarey, S. A., Zúñiga, E. C., & Vásquez‐Quitral, P. (2020) · International Journal of Food Properties · doi:10.1080/10942912.2020.1850775 · Cited by 10

Preclinical pharmacokinetics of trigonelline using ultra‐performance liquid chromatography–tandem mass spectrometry and pharmacological studies targeting type 2 diabetes

Wadhwa, G., Krishna, K. V., Taliyan, R., Tandon, N., Yadav, S. S., Banerjee, D., Narwaria, A., Katiyar, C. K., & Dubey, S. K. (2021) · Separation Science Plus · doi:10.1002/sscp.202000118 · Cited by 10

Callus induction and withanolides production through cell suspension culture of Withania coagulans (Stocks) Dunal

Mirjalili, M. H., & Esmaeili, H. (2022) · Journal of Medicinal Plants · doi:10.52547/jmp.21.81.79 · Cited by 10

Effect of roasting conditions on several chemical constituents of Vietnam Robusta coffee

Cuong, T. V., Ling, L. H., Quan, G. K., Tiep, T. D., Xia, N. A. N., Qing, C. X., & Linh, T. L. (2014) · The Annals of the University Dunarea de Jos of Galati Fascicle VI – Food Technology · Cited by 10

Medicinal Plants as Novel Promising Therapeutics for Neuroprotection and Neuroregeneration

Kaur, G., Kataria, H., & Mishra, R. (2018) · Springer eBooks · doi:10.1007/978-981-10-8291-7_20 · Cited by 10

Natural Modulators of Amyloid-Beta Precursor Protein Processing.

Zhang, C., & Tanzi, R. E. (2012) · PubMed · Cited by 9

Neuroprotective Effect of Ayurvedic Preparations and Natural Products on Parkinson's Disease

Borah, A., Choudhury, A., Paul, R. K., Mazumder, M. K., & Chetia, S. (2017) · Wiley eBooks · doi:10.1002/9783527803781.ch5 · Cited by 9

Iodixanol activation of mast cells: Implications in the pathogenesis of iodixanol-induced delayed cutaneous adverse reactions

Zou, W., Yang, S., Chen, L., Hu, S., Hao, G., & Hu, C. (2021) · Toxicology · doi:10.1016/j.tox.2021.153034 · Cited by 8

Elicitation Improves the Production of Bioactive Compounds and Antioxidant Activity in Cell Suspension Culture of Withania coagulans (Stocks) Dunal

Dorrazehi, M., Allahdou, M., Fakheri, B. A., & Mehravaran, L. (2024) · Russian Journal of Plant Physiology · doi:10.1134/s1021443724603835 · Cited by 8

Cognitive improvement by ginseng in Alzheimer's disease

Lee, S. (2007) · Journal of Ginseng Research · doi:10.5142/jgr.2007.31.1.051 · Cited by 8

Green coffee beans

Garg, S. K., Shukla, A. K., & Choudhury, S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821038-3.00042-2 · Cited by 10

Nutraceuticals Neuroprotect Naturally

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