Assessment of Direct Shoot Organogenesis and Genetic Fidelity in Solanum viarum Dunal—A Commercially Important Medicinal Plant

A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures

Murashige, T., & Skoog, F. K. (1962) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1962.tb08052.x · Cited by 67,420 · see citing works

Colorimetry of Total Phenolics with Phosphomolybdic-Phosphotungstic Acid Reagents

Singleton, V. L., & Rossi, J. A. (1965) · American Journal of Enology and Viticulture · doi:10.5344/ajev.1965.16.3.144 · Cited by 24,852 · see citing works

Rapid Flow Cytometric Analysis of the Cell Cycle in Intact Plant Tissues

Galbraith, D. W., Harkins, K. R., Maddox, J. M., Ayres, N. M., Sharma, D. P., & Firoozabady, E. (1983) · Science · doi:10.1126/science.220.4601.1049 · Cited by 1,948 · see citing works

Plant DNA Flow Cytometry and Estimation of Nuclear Genome Size

Doležel, J. (2004) · Annals of Botany · doi:10.1093/aob/mci005 · Cited by 1,054 · see citing works

Analysis of Nuclear DNA content in plant cells by Flow cytometry

Dpooležel, J., Binarová, P., & Lcretti, S. (1989) · Biologia Plantarum · doi:10.1007/bf02907241 · Cited by 675 · see citing works

Somaclonal variations and their applications in horticultural crops improvement

Krishna, H., Alizadeh, M., Singh, D., Singh, U., Chauhan, N., Eftekhari, M., & Sadh, R. K. (2016) · 3 Biotech · doi:10.1007/s13205-016-0389-7 · Cited by 436 · see citing works

Regeneration in plants and animals: dedifferentiation, transdifferentiation, or just differentiation?

Sugimoto, K., Gordon, S., & Meyerowitz, E. M. (2011) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.12.004 · Cited by 349 · see citing works

Thidiazuron: A multi-dimensional plant growth regulator

Guo, B., Abbasi, B. H., Amir, Z., L, L. X., & Y, H. W. (2011) · AFRICAN JOURNAL OF BIOTECHNOLOGY · doi:10.5897/ajb11.636 · Cited by 302 · see citing works

Herbal medicines used in the treatment of diabetes mellitus in Arunachal Himalaya, northeast, India

Tag, H., Kalita, P., Dwivedi, P., Das, A. K., & Namsa, N. D. (2012) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2012.03.007 · Cited by 131 · see citing works

Changes in phenol content during strawberry (Fragaria×ananassa, cv. Chandler) callus culture

Arnaldos, T. L., Muñoz, R., Ferrer, M. Á., & Calderón, A. A. (2001) · Physiologia Plantarum · doi:10.1034/j.1399-3054.2001.1130303.x · Cited by 115 · see citing works

Detection of somaclonal variation of cotton (Gossypium hirsutum) using cytogenetics, flow cytometry and molecular markers

Jin, S., Mushke, R., Zhu, H., Tu, L., Lin, Z., Zhang, Y., & Zhang, X. (2008) · Plant Cell Reports · doi:10.1007/s00299-008-0557-2 · Cited by 113 · see citing works

Tissue browning of in vitro cultures of Scots pine: Role of peroxidase and polyphenol oxidase

Laukkanen, H., Häggman, H., Kontunen‐Soppela, S., & Hohtola, A. (1999) · Physiologia Plantarum · doi:10.1034/j.1399-3054.1999.106312.x · Cited by 101 · see citing works

Medicinal significance, pharmacological activities, and analytical aspects of solasodine: A concise report of current scientific literature

Patel, K., Singh, R. B., & Patel, D. K. (2013) · Journal of Acute Disease · doi:10.1016/s2221-6189(13)60106-7 · Cited by 90 · see citing works

Changes in the steroidal alkaloid solasodine during development of Solanum nigrum and Solanum incanum

Eltayeb, E. A., Al-Ansari, A., & Roddick, J. G. (1997) · Phytochemistry · doi:10.1016/s0031-9422(97)00323-3 · Cited by 89 · see citing works

Plant Tissue Culture: An Alternative for Production of Useful Metabolites

Misawa, M. (1994) · Cited by 86 · see citing works

Methyl jasmonate elicits the solasodine production and anti-oxidant activity in hairy root cultures of Solanum trilobatum L.

Shilpha, J., Satish, L., Kavikkuil, M., Largia, M. J. V., & Ramesh, M. (2015) · Industrial Crops and Products · doi:10.1016/j.indcrop.2015.03.083 · Cited by 78 · see citing works

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 · see citing works

Haematological studies on the ethanolic stem bark extract of Pterocarpus erinaceus poir ( fabaceae )

Oa, S., Aliyu, M. R., & Tijani, A. (2008) · AFRICAN JOURNAL OF BIOTECHNOLOGY · doi:10.5897/ajb07.393 · Cited by 76 · see citing works

Inhibition ofTrypanosoma cruziGrowthin vitrobySolanumAlkaloids: A Comparison with Ketoconazole

Chataing, B., Concepción, J. L., Lobaton, R. J., & Usubillaga, A. N. (1998) · Planta Medica · doi:10.1055/s-2006-957361 · Cited by 67 · see citing works

Direct shoot regeneration from lamina explants of two commercial cut flower cultivars of Anthurium andraeanum Hort.

Martin, K. P., Joseph, D., Madasser, J., & Philip, V. J. (2003) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1079/ivp2003460 · Cited by 64 · see citing works

Sugarcane micropropagation and phenolic excretion

Lorenzo, J. C., de los Angeles Blanco, M., Peláez, O., González, A., Cid, M., Iglesias, A., González, B., Escalona, M., Espinosa, P., & Borroto, C. (2001) · Plant Cell, Tissue and Organ Culture · doi:10.1023/a:1010666115337 · Cited by 61 · see citing works

Analysis of genetic stability of in vitro propagated potato microtubers using DNA markers

Tiwari, J. K., Chandel, P., Gupta, S., Gopal, J., Singh, B. P., & Bhardwaj, V. (2013) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-013-0190-6 · Cited by 59 · see citing works

Shoot regeneration from leaf explants of Withania coagulans (Stocks) Dunal and genetic stability evaluation of regenerates with RAPD and ISSR markers

Rathore, M. S., Mastan, S. G., Yadav, P. K., Bhatt, V., Shekhawat, N. S., & Chikara, J. (2015) · South African Journal of Botany · doi:10.1016/j.sajb.2015.08.003 · Cited by 53 · see citing works

Transcriptome analysis provides insight into prickle development and its link to defense and secondary metabolism in Solanum viarum Dunal

Pandey, S., Goel, R., Bhardwaj, A., Asif, M. H., Sawant, S. V., & Misra, P. (2018) · Scientific Reports · doi:10.1038/s41598-018-35304-8 · Cited by 53 · see citing works

Direct shoot organogenesis and assessment of genetic stability in regenerants of Solanum aculeatissimum Jacq.

Ghimire, B. K., Yu, C. Y., & Chung, I. (2011) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-011-0057-x · Cited by 50 · see citing works

Genome size analysis of field grown and tissue culture regenerated Rauvolfia serpentina (L) by flow cytometry: Histology and scanning electron microscopic study for in vitro morphogenesis

Zafar, N., Mujib, A., Ali, M., Tonk, D., Gulzar, B., Malik, M. Q., Sayeed, R., & Mamgain, J. (2018) · Industrial Crops and Products · doi:10.1016/j.indcrop.2018.11.049 · Cited by 42 · see citing works

Efficiency of direct and indirect shoot organogenesis in different genotypes of Rosa hybrida

Pourhosseini, L., Kermani, M. J., Habashi, A. A., & Khalighi, A. (2012) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-012-0210-1 · Cited by 39 · see citing works

High efficiency organogenesis and analysis of genetic stability of the regenerants in Solanum melongena

Xing, Y., Yao, Y., Luo, X., Zhang, J. N., Zhao, B., & Guo, Y. (2010) · Biologia Plantarum · doi:10.1007/s10535-010-0041-z · Cited by 36 · see citing works

Application of EST-SSRs to examine genetic diversity in eggplant and its close relatives

Tümbilen, Y., Frary, A., Daunay, M., & Doğanlar, S. (2011) · TURKISH JOURNAL OF BIOLOGY · doi:10.3906/biy-0906-57 · Cited by 34 · see citing works

In vitro regeneration of Solanum nigrum with enhanced solasodine production

Bhat, M. A., Mujib, A., Junaid, A., & Mahmooduzzafar, M. (2010) · Biologia Plantarum · doi:10.1007/s10535-010-0136-6 · Cited by 34 · see citing works

Efficient and reproducible in vitro regeneration of Solanum lycopersicum and assessment genetic uniformity using flow cytometry and SPAR methods

Alatar, A. A., Faisal, M., Abdel-Salam, E. M., Canto, T., Saquib, Q., Javed, S. B., El‐Sheikh, M. A., & Al-Khedhairy, A. A. (2017) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2017.03.008 · Cited by 31 · see citing works

Medicinal plants used by the Malayali tribe of Servarayan hills, Yercad, Salem district, Tamil Nadu, India

Udayan, P. S., George, S., Tushar, K. V., & Balachandran, I. (2006) · Zoos Print Journal · doi:10.11609/jott.zpj.1426a.2223-4 · Cited by 22 · see citing works

Somatic embryogenesis from in vitro anther culture of apomictic buffel grass genotypes and analysis of regenerated plants using flow cytometry

Carloni, E., Ribotta, A., Colomba, E. L., Griffa, S., Quiroga, M., Tommasino, E., & Grunberg, K. (2014) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-014-0441-4 · Cited by 21 · see citing works

Efficient in vitro plant regeneration from seedling-derived explants and genetic stability analysis of regenerated plants of Simarouba glauca DC. by RAPD and ISSR markers

Bramhanapalli, M., Thogatabalija, L., & Gudipalli, P. (2016) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-016-9795-0 · Cited by 21 · see citing works

Anti-inflammatory and anthelmintic activities ofSolanum khasianumClarke

Jarald, E. E., Edwin, S., Saini, V., Deb, L., Gupta, V., Wate, S., & Busari, K. (2008) · Natural Product Research · doi:10.1080/14786410701590590 · Cited by 21 · see citing works

Regeneration efficiency based on genotype, culture condition and growth regulators of eggplant (Solanum melongena L.)

Muktadir, M. A., Habib, M. A., Mian, M. A. K., & Akhond, M. A. Y. (2016) · Agriculture and Natural Resources · doi:10.1016/j.anres.2014.10.001 · Cited by 20 · see citing works

Influence of auxins in direct in vitro morphogenesis of Euphorbia nivulia, a lectinaceous medicinal plant

Martin, K. P., Sunandakumari, C., Chithra, M., & Madhusoodanan, P. V. (2005) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1079/ivp2004615 · Cited by 20 · see citing works

Direct regeneration of plants derived from in vitro cultured shoot tips and leaves of three Lysimachia species

Zheng, W., Xu, X., Dai, H., & Chen, L.-Q. (2009) · Scientia Horticulturae · doi:10.1016/j.scienta.2009.03.018 · Cited by 19 · see citing works

Growth and alkaloid production along with expression profiles of biosynthetic pathway genes in two contrasting morphotypes of prickly and prickleless Solanum viarum Dunal

Prasad, A., Patel, P., Pandey, S., Niranjan, A., & Misra, P. (2019) · PROTOPLASMA · doi:10.1007/s00709-019-01446-3 · Cited by 18 · see citing works

Direct shoot regeneration from leaf and internode explants of Aloysia polystachya [GRIS.] mold. (Verbenaceae)

Burdyn, L., Luna, C. V., Tarracó, J., Sansberro, P. A., Dudit, N., Conzález, A., & Mrocinski, L. (2006) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1079/ivp2006751 · Cited by 17 · see citing works

Genetic variability in regenerated plants of Ungernia victoris

Bublyk, O. M., Andreev, I. O., Spiridonova, K. V., & Kunakh, V. A. (2012) · Biologia Plantarum · doi:10.1007/s10535-012-0106-2 · Cited by 16 · see citing works

Effect of 2,4-D; BAP and TDz on callus induction and shoot regeneration in potato.

Sherkar, H. D., & Chavan, A. (2014) · Cited by 12 · see citing works

Direct Differentiation of Shoot Buds from Leaf Explants of Cajanus Cajan L.

Misra, P. (2002) · Biologia Plantarum · doi:10.1023/a:1016205331021 · Cited by 12 · see citing works

EVALUATION OF ANTI-OBESITY ACTIVITY OF SOLASODINE IN HIGH FAT DIET-INDUCED OBESITY IN RAT

Khaserao, S., & Somani, R. S. (2017) · International Journal of Pharmacy and Pharmaceutical Sciences · doi:10.22159/ijpps.2017v9i3.16025 · Cited by 9 · see citing works

Efficient protocol for in vitro callus induction and indirect plant regeneration of Solanum viarum (Dunal) - An important anticancer medicinal plant

Mahadev, M. D., Panathula, C. S., & Naidu, C. V. (2014) · International journal of medicinal and aromatic plants · Cited by 7 · see citing works

Effects of Solanum viarum cuticular leaf extracts and its fractions on the oviposition of Helicoverpa armigera (Hubner) (Lepidoptera: Noctuidae)

Diongue, A., Lai, P. Y., Chang, Y., & Lin, C. (2005) · Cited by 6 · see citing works

At the border of the unknown—a plea for curiosity

Nick, P. (2020) · PROTOPLASMA · doi:10.1007/s00709-019-01478-9 · Cited by 6 · see citing works

Somaclonal variations as a mean for obtaining regenerants with different growth rates in poplar (Populus × berolinensis Dipp.)

Gamburg, K. Z., & Войников, В. К. (2013) · Natural Science · doi:10.4236/ns.2013.55075 · Cited by 5 · see citing works

Survey of medicinal plants used against leprosy disease by the tribal (Lalung) people of Myong area of Morigaon District, Assam, India.

Deka, S., & Deka, S. P. (2007) · PLANT ARCHIVES · Cited by 5 · see citing works

A comparative study of in vitro regeneration of shoots in different cultivars of Gerbera jamesonii H. bolus ex hook. F.

Misra, P., Purshottam, D. K., Siddiqui, S., Jain, M., & Toppo, D. D. (2010) · Propagation of Ornamental Plants · Cited by 3 · see citing works

Germination improvement through alleviation of seed hardness in Solanum viarum Dunal.

Ramamoorthy, K., Geetha, R., & Sujatha, K. (2010) · International Journal of Plant Sciences Muzaffarnagar · Cited by 2 · see citing works

Effect of antioxidant protection system on regeneration potential of different chemotypes of Withania somnifera (L.) Dunal ― A comparative analysis

Singh, G., Saema, S., Singh, S., & Misra, P. (2017) · Cited by 2 · see citing works

Somaclonal Variation and Clonal Fidelity in Commercial Micropropagation: Challenges and Perspectives

Majumder, S., Igamberdiev, A. U., & Debnath, S. C. (2025) · Agronomy · doi:10.3390/agronomy15061489 · Cited by 46 · see citing works

Efficient in vitro plant regeneration from leaf-derived callus and genetic fidelity assessment of an endemic medicinal plant Ranunculus wallichianus Wight & Arnn by using RAPD and ISSR markers

Srinivasan, P., Raja, H. D., & Tamilvanan, R. (2021) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-021-02134-y · Cited by 28 · see citing works

Assessing the Genetic Stability of In Vitro Raised Plants

Rohela, G. K., Jogam, P., Saini, P. K., Sandhya, D., Peddaboina, V., & Shekhawat, M. S. (2022) · Springer eBooks · doi:10.1007/978-981-19-0055-6_11 · Cited by 22 · see citing works

Genotype-dependent and temperature-induced modulation of secondary metabolites, antioxidative defense and gene expression profile in Solanum viarum Dunal

Patel, P., Prasad, A., Srivastava, D., Niranjan, A., Saxena, G., Singh, S. S., Misra, P., & Chakrabarty, D. (2021) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2021.104686 · Cited by 20 · see citing works

Biotechnological Tools for Conservation of Plant Genetic Diversity

Agrawal, A., Gowthami, R., Chander, S., Srivastava, V., Shankar, M., & Deepak, D. A. (2024) · Sustainable development and biodiversity · doi:10.1007/978-981-99-5245-8_21 · Cited by 13 · see citing works

Axenic rhizome culture and genetic fidelity assessment of Eulophia dabia (D. Don) Hochr: an endangered terrestrial orchid species

Panwar, G. S., Joshi, B., & Joshi, R. (2022) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-022-10258-9 · Cited by 12 · see citing works

Growth, phytochemical and gene expression changes related to the secondary metabolite synthesis of Solanum viarum Dunal

Patel, P., Prasad, A., Gupta, S. C., Niranjan, A., Lehri, A., Singh, S. S., Misra, P., & Chakrabarty, D. (2021) · Industrial Crops and Products · doi:10.1016/j.indcrop.2021.113464 · Cited by 11 · see citing works

Molecular Markers in Assessing Genetic Clonal Fidelity for in Vitro Propagated Endangered Medicinal Plants

Biswas, P., Nandy, S., Dey, A., Tikendra, L., & Nongdam, P. (2022) · Springer eBooks · doi:10.1007/978-981-16-6005-4_6 · Cited by 10 · see citing works

In vitro propagation, genetic and phytochemical fidelity in Glycyrrhiza glabra L., a potent glycyrrhizin yielding endangered plant

Ayangla, N. W., Dwivedi, P., Dey, A., & Pandey, D. K. (2022) · The Nucleus · doi:10.1007/s13237-022-00395-2 · Cited by 10 · see citing works

Revisiting the ethnomedicinal, ethnopharmacological, phytoconstituents and phytoremediation of the plant Solanum viarum Dunal

Thakur, M., Verma, R., Kumar, D., Das, P. P., Dhalaria, R., Kumar, A., Kuča, K., Azizov, S., & Kumar, D. (2024) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-024-03034-6 · Cited by 12 · see citing works

Biotic elicitor–induced changes in growth, antioxidative defense, and metabolites in an improved prickleless Solanum viarum

Prasad, A., Patel, P., Niranjan, A., Mishra, A., Saxena, G., Singh, S. S., & Chakrabarty, D. (2022) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-022-12159-8 · Cited by 7 · see citing works

Phytochemical variability during vegetation of Chamerion angustifolium (L.) Holub genotypes derived from in vitro cultures

Dreger, M., Seidler-Łożykowska, K., Szalata, M., Adamczak, A., & Wielgus, K. (2021) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-021-02154-8 · Cited by 7 · see citing works

In vitro regeneration through indirect organogenesis, genetic uniformity analysis and mineral content determination of finger millet (Eleusine coracana L.)

Kansara, R. V., Solanki, V. H., Srivashtav, V., Patel, R. M., Gandhi, K. D., & Mehta, V. S. (2022) · Biologia · doi:10.1007/s11756-022-01179-4 · Cited by 5 · see citing works

Direct regeneration from leaf explants and genetic fidelity analysis of regenerates through ISSR markers in Kedrostis foetidissima: a medicinal climber

Kommidi, S., Sandhya, D., Koppula, T., & Mohammed, M. S. (2023) · Vegetos · doi:10.1007/s42535-023-00713-2 · Cited by 3 · see citing works

Bioactive Compounds in Solanum viarum: Medicinal Properties, In Vitro Propagation, and Conservation

Pandey, S., & Sawant, S. V. (2023) · Springer eBooks · doi:10.1007/978-981-99-2824-8_8 · Cited by 2 · see citing works

Genetic fidelity assessment of in vitro-regenerated medicinal plants: cytological, chromatographic, and molecular marker-based approaches

Jogam, P., Rohela, G. K., Aileni, M., Sandhya, D., Singisala, N. R., & Peddaboina, V. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-43944-5.00008-6

Efficient protocol for direct shoot organogenesis from in vitro raised nodal explants of Solanum viarum (Dunal) - an important anticancer medicinal plant.

Mahadev, M. D., Panathula, C. S., & Naidu, C. V. (2014) · International journal of medicinal and aromatic plants · Cited by 3 · see citing works

Improved in vitro propagation, solasodine accumulation and assessment of clonal fidelity in regenerants of Solanum trilobatum L. by flow cytometry and SPAR methods

Shilpha, J., Silambarasan, T., Largia, M. J. V., & Ramesh, M. (2014) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-013-0420-1 · Cited by 31 · see citing works

Rapid, reliable plantlet regeneration, hairy root induction and in vitro potential for solasodine alkaloid accumulation in an important medicinal plant Solanum virginianum

Dalavi, C. M., Naravula, J., Kishor, P. B. K., & Patil, S. A. (2023) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-023-02459-w · Cited by 16 · see citing works

Growth, phytochemical and gene expression changes related to the secondary metabolite synthesis of Solanum viarum Dunal

Patel, P., Prasad, A., Gupta, S. C., Niranjan, A., Lehri, A., Singh, S. S., Misra, P., & Chakrabarty, D. (2021) · Industrial Crops and Products · doi:10.1016/j.indcrop.2021.113464 · Cited by 11 · see citing works

Highly efficient rapid micropropagation and assessment of genetic fidelity of regenerants by ISSR and SCoT markers of Solanum khasianum Clarke

Chirumamilla, P., Gopu, C., Jogam, P., & Taduri, S. (2020) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-020-01964-6 · Cited by 74 · see citing works