Micropropagation, Estimation of DNA Methylation during Multiplication Cycles and Mycorrhization of Seed-Derived Dendrocalamus asper (Schultes f.) Backer Ex Heyne

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

Reciprocal Rewards Stabilize Cooperation in the Mycorrhizal Symbiosis

Kiers, E. T., Duhamel, M., Beesetty, Y., Mensah, J. A., Franken, O., Verbruggen, E., Fellbaum, C. R., Kowalchuk, G. A., Hart, M. M., Bago, A., et al. (2011) · Science · doi:10.1126/science.1208473 · Cited by 1,800 · see citing works

Roles of Arbuscular Mycorrhizas in Plant Phosphorus Nutrition: Interactions between Pathways of Phosphorus Uptake in Arbuscular Mycorrhizal Roots Have Important Implications for Understanding and Manipulating Plant Phosphorus Acquisition

Smith, S. E., Jakobsen, I., Grønlund, M., & SMITH, F. A. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.174581 · Cited by 1,250 · see citing works

Early events of vesicular–arbuscular mycorrhiza formation on Ri T‐DNA transformed roots

Bécard, G., & Fortin, J. A. (1988) · New Phytologist · doi:10.1111/j.1469-8137.1988.tb03698.x · Cited by 863 · see citing works

Morpho-physiological disorders in in vitro culture of plants

Hazarika, B. N. (2006) · Scientia Horticulturae · doi:10.1016/j.scienta.2006.01.038 · Cited by 507 · see citing works

Regulation of root hair density by phosphorus availability in Arabidopsis thaliana

Ma, Z., Bielenberg, D. G., Brown, K. M., & Lynch, J. P. (2001) · Plant Cell & Environment · doi:10.1046/j.1365-3040.2001.00695.x · Cited by 436 · see citing works

DNA and histone methylation in plants

Tariq, M., & Paszkowski, J. (2004) · Trends in Genetics · doi:10.1016/j.tig.2004.04.005 · Cited by 262 · see citing works

Epigenetics in plant tissue culture

Smulders, M. J. M., & de Klerk, G. J. (2011) · Plant Growth Regulation · doi:10.1007/s10725-010-9531-4 · Cited by 249 · see citing works

Meta‐topolin, an alternative to benzyladenine in tissue culture?

Werbrouck, S., Strnad, M., Onckelen, H. A. V., & Debergh, P. (1996) · Physiologia Plantarum · doi:10.1034/j.1399-3054.1996.980210.x · Cited by 242 · see citing works

Optimizing the micropropagation protocol for the endangered Aloe polyphylla: can meta-topolin and its derivatives serve as replacement for benzyladenine and zeatin?

Bairu, M. W., Stirk, W. A., Doležal, K., & Staden, J. V. (2007) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-007-9233-4 · Cited by 219 · see citing works

Mechanisms Underlying Establishment of Arbuscular Mycorrhizal Symbioses

Choi, J., SUMMERS, W. C., & Paszkowski, U. (2018) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-080516-035521 · Cited by 215 · see citing works

Topolins: A panacea to plant tissue culture challenges?

Aremu, A. O., Bairu, M. W., Doležal, K., Finnie, J. F., & Staden, J. V. (2011) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-011-0007-7 · Cited by 213 · see citing works

Protocols for Micropropagation of Woody Trees and Fruits

Jain, S. M., & Häggman, H. (2007) · Springer eBooks · doi:10.1007/978-1-4020-6352-7 · Cited by 200 · see citing works

Involvement of DNA methylation in tree development and micropropagation

Valledor, L., Hasbún, R., Meijón, M., Rodriguez, J. L., Santamaria, M. E., Viejo, M. D., Berdasco, M., Feito, I., Fraga, M. F., Cañal, M. J., et al. (2007) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-007-9262-z · Cited by 145 · see citing works

Bacteria in the plant tissue culture environment

Orlikowska, T. K., Nowak, K., & Reed, B. M. (2016) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-016-1144-9 · Cited by 133 · see citing works

Potential Role and Utilization of Plant Growth Promoting Microbes in Plant Tissue Culture

Soumaré, A., Diédhiou, A. G., Arora, N. K., Al‐Ani, L. K. T., Ngom, M., Fall, S., Hafidi, M., Ouhdouch, Y., Kouisni, L., & Sy, M. O. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.649878 · Cited by 129 · see citing works

Development of an autotrophic culture system for the in vitro mycorrhization of potato plantlets

Voets, L., de Boulois, H. D., Renard, L., Strullu, D. G., & Declerck, S. (2005) · FEMS Microbiology Letters · doi:10.1016/j.femsle.2005.05.025 · Cited by 106 · see citing works

Mechanisms of cytokinin action

Brault, M., & Maldiney, R. (1999) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(99)80046-1 · Cited by 104 · see citing works

5-azacytidine promotes microspore embryogenesis initiation by decreasing global DNA methylation, but prevents subsequent embryo development in rapeseed and barley

Solís, M., El-Tantawy, A.-A., Cano, V., Risueño, M. C., & Testillano, P. S. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00472 · Cited by 101 · see citing works

Meta-topolin Improves In Vitro Morphogenesis, Rhizogenesis and Biochemical Analysis in Pterocarpus marsupium Roxb.: A Potential Drug-Yielding Tree

Ahmad, A., & Anis, M. (2019) · Journal of Plant Growth Regulation · doi:10.1007/s00344-018-09910-9 · Cited by 97 · see citing works

In vitro propagation of the bamboo (Bambusa tulda Roxb.) through shoot proliferation

Saxena, S. (1990) · Plant Cell Reports · doi:10.1007/bf00232266 · Cited by 88 · see citing works

Update on White Lupin Cluster Root Acclimation to Phosphorus Deficiency Update on Lupin Cluster Roots

Cheng, L., Bucciarelli, B., Shen, J., Allan, D. L., & Vance, C. P. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.175174 · Cited by 79 · see citing works

Evaluation of genetic fidelity of in vitro raised plants of Dendrocalamus asper (Schult. & Schult. F.) Backer ex K. Heyne using DNA-based markers

Singh, S. R., Dalal, S., Singh, R., Dhawan, A. K., & Kalia, R. K. (2012) · Acta Physiologiae Plantarum · doi:10.1007/s11738-012-1084-x · Cited by 71 · see citing works

In vitro propagation of bamboo species through axillary shoot proliferation: a review

Sandhu, M., Wani, S. H., & Jiménez, V. M. (2017) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-017-1325-1 · Cited by 71 · see citing works

Micorriza arbuscular e a tolerância das plantas ao estresse

Folli‐Pereira, M. D. S., Meira-Haddad, L. S., Bazzolli, D. M. S., & Kasuya, M. C. M. (2012) · Revista Brasileira de Ciência do Solo · doi:10.1590/s0100-06832012000600001 · Cited by 70 · see citing works

Micropropagation of Dendrocalamus asper by shoot proliferation using seeds

Arya, S., Sharma, P., Kaur, R., & Arya, I. D. (1999) · Plant Cell Reports · doi:10.1007/s002990050678 · Cited by 66 · see citing works

Meta-topolin and liquid medium mediated enhanced micropropagation via ex vitro rooting in Vanilla planifolia Jacks. ex Andrews

Manokari, M., Priyadharshini, S., Jogam, P., Dey, A., & Shekhawat, M. S. (2021) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-021-02044-z · Cited by 61 · see citing works

Meta-Topolin (mT) enhances the in vitro regeneration frequency of Sesamum indicum (L.)

Elayaraja, D., Subramanyam, K., Vasudevan, V., Sathish, S., Kasthurirengan, S., Ganapathi, A., & Manickavasagam, M. (2019) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2019.101320 · Cited by 61 · see citing works

Methylome reorganization during in vitro dedifferentiation and regeneration of Populus trichocarpa

Vining, K. J., Pomraning, K., Wilhelm, L., Ma, C., Pellegrini, M. A., Di, Y., Mockler, T. C., Freitag, M., & Strauss, S. H. (2013) · BMC Plant Biology · doi:10.1186/1471-2229-13-92 · Cited by 59 · see citing works

A Concise Review of Dendrocalamus asper and Related Bamboos: Germplasm Conservation, Propagation and Molecular Biology

Mustafa, A. A., Derise, M. R., Yong, W. T. L., & Rodrigues, K. F. (2021) · Plants · doi:10.3390/plants10091897 · Cited by 52 · see citing works

Young bamboo culm flour of Dendrocalamus asper: Technological properties for food applications

Felisberto, M. H. F., Beraldo, A. L., & Clerici, M. T. P. S. (2016) · LWT · doi:10.1016/j.lwt.2016.06.015 · Cited by 51 · see citing works

Micropropagation of Dendrocalamus asper {Schult. & Schult. F.} Backer ex k. Heyne): an exotic edible bamboo

Singh, S. R., Dalal, S., Singh, R., Dhawan, A. K., & Kalia, R. K. (2011) · Journal of Plant Biochemistry and Biotechnology · doi:10.1007/s13562-011-0095-9 · Cited by 49 · see citing works

Compatibilidade simbiótica de fungos micorrízicos arbusculares com espécies arbóreas tropicais

Rojas, E. P., Siqueira, J. O., & dos Santos, J. G. D. (2006) · Revista Brasileira de Ciência do Solo · doi:10.1590/s0100-06832006000300003 · Cited by 48 · see citing works

Physiological differences and changes in global DNA methylation levels in Agave angustifolia Haw. albino variant somaclones during the micropropagation process

Duarte-Aké, F., Castillo-Castro, E., Pool, F. B., Espadas, F., Santamaría, J. M., Robert, M. L., & De-la-Peña, C. (2016) · Plant Cell Reports · doi:10.1007/s00299-016-2049-0 · Cited by 48 · see citing works

Variations in leaf morphology and DNA methylation following in vitro culture of Malus xiaojinensis

Huang, H., Han, S. S., Wang, Y. N., Zhang, X., & Han, Z. H. (2012) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-012-0179-9 · Cited by 45 · see citing works

Application of meta-Topolin for improving micropropagation of gooseberry (Ribes grossularia)

Kucharska, D., Orlikowska, T. K., Maciorowski, R., Kunka, M., Wójcik, D., & Pluta, S. (2020) · Scientia Horticulturae · doi:10.1016/j.scienta.2020.109529 · Cited by 44 · see citing works

Expression and DNA methylation of SERK, BBM, LEC2 and WUS genes in in vitro cultures of Boesenbergia rotunda (L.) Mansf.

Karim, R., Tan, Y. S., Singh, P., Khalid, N., & Harikrishna, J. A. (2018) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-018-0566-8 · Cited by 43 · see citing works

Growth response of cacao (Theobroma cacao L.) plant as affected by bamboo biochar and arbuscular mycorrhizal fungi in sterilized and unsterilized soil

Aggangan, N. S., Cortes, A. D., & Reaño, C. E. (2019) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2019.101347 · Cited by 43 · see citing works

Arbuscular mycorrhizal fungi and micropropagation of high value crops

Vestberg, M. V., Cassells, A. C., Schubert, A., Cordier, C., & Gianinazzi, S. (2002) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-8117-3_18 · Cited by 43 · see citing works

Cell Biology: Control of Partner Lifetime in a Plant–Fungus Relationship

Gutjahr, C., & Parniske, M. (2017) · Current Biology · doi:10.1016/j.cub.2017.04.020 · Cited by 41 · see citing works

Target of Rapamycin Regulates Genome Methylation Reprogramming to Control Plant Growth in Arabidopsis

Zhu, T., Li, L., Feng, L., Mo, H., & Ren, M. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00186 · Cited by 39 · see citing works

Effect of arbuscular mycorrhizal fungal isolates and organic manure on growth and mycorrhization of micropropagated Dendrocalamus asper plantlets and on spore production in their rhizosphere

Verma, R. K., & Arya, I. D. (1998) · Mycorrhiza · doi:10.1007/s005720050221 · Cited by 33 · see citing works

Meta-Topolin mediated improved micropropagation, foliar micro-morphological traits, biochemical profiling, and assessment of genetic fidelity in Santalum album L.

Manokari, M., Mehta, S. R., Priyadharshini, S., Badhepuri, M. K., Sandhya, D., Jayaprakash, K., Cokul Raj, M., Dey, A., Rajput, B. S., & Shekhawat, M. S. (2021) · Industrial Crops and Products · doi:10.1016/j.indcrop.2021.113931 · Cited by 32 · see citing works

A two step method for accelerated mass propagation of Dendrocalamus asper and their evaluation in field

Banerjee, M., Gantait, S., & Pramanik, B. R. (2011) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-011-0088-0 · Cited by 32 · see citing works

Effect of nodal positions, seasonal variations, shoot clump and growth regulators on micropropagation of commercially important bamboo, Bambusa nutans Wall. ex. Munro

Mudoi, K. D., Saikia, S. P., & Mina, B. (2014) · AFRICAN JOURNAL OF BIOTECHNOLOGY · doi:10.5897/ajb2014.13659 · Cited by 32 · see citing works

Ontogeny ofGlomus clarum, in Ri T-DNA transformed roots

de Souza, F. A., & Berbara, R. L. L. (1999) · Mycologia · doi:10.1080/00275514.1999.12061024 · Cited by 32 · see citing works

An Effective Protocol for Micropropagation of Edible Bamboo Species (Bambusa tuldaandMelocanna baccifera) through Nodal Culture

Waikhom, S. D., & Louis, B. (2014) · The Scientific World JOURNAL · doi:10.1155/2014/345794 · Cited by 31 · see citing works

Variations of DNA methylation in Eucalyptus urophylla×Eucalyptus grandis shoot tips and apical meristems of different physiological ages

Mankessi, F., Saya, A. R., Favreau, B., Doulbeau, S., Conéjéro, G., Lartaud, M., Verdeil, J., & Monteuuis, O. (2011) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2011.01491.x · Cited by 26 · see citing works

Cytological, genetical and phytochemically stable meta-Topolin (mT) - induced mass propagation of underutilized Physalis minima L. for production of withaferin A

Halder, T., & Ghosh, B. (2021) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2021.102012 · Cited by 25 · see citing works

Regeneration Technique of Bamboo Species through Nodal Segments: A Review

Suwal, M. M., Lamichhane, J., & Gauchan, D. P. (2020) · Nepal Journal of Biotechnology · doi:10.3126/njb.v8i1.30209 · Cited by 22 · see citing works

Effect of in vitro shoot multiplication and somatic embryogenesis on 5-methylcytosine content in DNA of Myrtus communis L.

Parra, R., Pastor, M. T., Pérez-Payá, E., & Amo-Marco, J. B. (2001) · Plant Growth Regulation · doi:10.1023/a:1017571911028 · Cited by 22 · see citing works

A role of age-dependent DNA methylation reprogramming in regulating the regeneration capacity of Boea hygrometrica leaves

Sun, R., Zuo, E.-H., Qi, J., Liu, Y., Lin, C.-T., & Deng, X. (2019) · Functional & Integrative Genomics · doi:10.1007/s10142-019-00701-3 · Cited by 20 · see citing works

Respostas fisiológicas em mudas de maracujazeiro amarelo (Passiflora edulis Sims. f. flavicarpa Deg.) inoculadas com fungos micorrízicos arbusculares e submetidas a estresse hídrico

Cavalcante, U. M. T., Maia, L. C., Nogueira, R. J. M. C., & dos Santos, V. F. (2001) · Acta Botanica Brasilica · doi:10.1590/s0102-33062001000300008 · Cited by 20 · see citing works

Effects of Vitrofural, BAP and meta-Topolin in the in vitro culture of Dendrocalamus asper

Ornellas, T. S., Werner, D., Holderbaum, D. F., Scherer, R. F., & Guerra, M. P. (2017) · Acta Horticulturae · doi:10.17660/actahortic.2017.1155.41 · Cited by 16 · see citing works

The effect of densification on physical and mechanical properties of bamboo Dendrocalamus asper

Azadeh, A., de Sá, A. D., Kadivar, M., Gauss, C., & Savastano, H. (2022) · European Journal of Wood and Wood Products · doi:10.1007/s00107-022-01823-5 · Cited by 16 · see citing works

Effect of Arbuscular Mycorrhizal Inoculations on Seedling Growth and Biomass Productivity of Two Bamboo Species

Jha, A., Kumar, A., Saxena, R. K., Kamalvanshi, M., & Chakravarty, N. (2011) · Indian Journal of Microbiology · doi:10.1007/s12088-011-0213-3 · Cited by 15 · see citing works

Arbuscular Mycorrhizal Fungi Associated with Bamboo Under Cerrado Brazilian Vegetation

de Moura, J. B., de Souza, R. F., Vieira, W. G., Lima, I. R., Brito, G. H. M., & Marín, C. (2019) · Journal of soil science and plant nutrition · doi:10.1007/s42729-019-00093-0 · Cited by 15 · see citing works

Agromorphologic, genetic and methylation profiling of Dioscorea and Musa species multiplied under three micropropagation systems

Jekayinoluwa, T., Guèye, B., Bhattacharjee, R., Osibanjo, O., Shah, T. M., & Abberton, M. T. (2019) · PLoS ONE · doi:10.1371/journal.pone.0216717 · Cited by 13 · see citing works

Factors affecting "in vitro" plant development and root colonization of sweet potato by Glomus etunicatum Becker & Gerd

Bressan, W. (2002) · Brazilian Journal of Microbiology · doi:10.1590/s1517-83822002000100006 · Cited by 11 · see citing works

Utilization of Dendrocalamus Asper Backer Bamboo Charcoal and Pyroligneous Acid

Sumanatrakul, P., Kongsune, P., Chotitham, L., & Sukto, U. (2015) · Energy Procedia · doi:10.1016/j.egypro.2015.11.558 · Cited by 10 · see citing works

Micropropagation, plantlets production estimation and ISSR marker-based genetic fidelity analysis of Guadua magna and G. angustifólia

Nogueira, J. S., Gomes, H. T., & Scherwinski-Pereira, J. E. (2019) · Pesquisa Agropecuária Tropical · doi:10.1590/1983-40632019v4953743 · Cited by 9 · see citing works

Monoxenic Culture as a Tool to Study the Effect of the Arbuscular Mycorrhizal Symbiosis on the Physiology of Micropropagated Plantlets in Vitro and ex Vitro

Desjardins, Y., Hernández‐Sebastià, C., & Piché, Y. (2005) · Springer eBooks · doi:10.1007/3-540-27331-x_10 · Cited by 4 · 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

Unlocking the hidden power of bamboo rhizomes: A comprehensive review of their role in nutrient storage, water retention, and plant growth

Kotangale, P., Agashe, A., Sawarkar, R., Dewangan, C., Tijare, G., & Singh, L. (2025) · Advances in Bamboo Science · doi:10.1016/j.bamboo.2025.100122 · Cited by 18 · see citing works

In Vitro Mycorrhization for Plant Propagation and Enhanced Resilience to Environmental Stress: A Review

Radi, H., Koufan, M., Belkoura, I., Koussa, T., & Mazri, M. A. (2025) · Plants · doi:10.3390/plants14142097 · Cited by 7 · see citing works

In vitro mycorrhization improves rooting, acclimatization and physiological traits of argan (Argania spinosa (L.) Skeels) plants propagated by microcuttings and micrografting

Radi, H., Koufan, M., Bouchiha, F., Elmaataoui, S., Kharbouche, H. A., Belkoura, I., Naciri, R., Koussa, T., & Mazri, M. A. (2025) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-025-03264-3 · Cited by 4 · see citing works

A scalable in vitro mycorrhization system enhances abiotic stress tolerance and acclimatization survival of argan (Argania spinosa (L.) Skeels) seedlings

Radi, H., Koufan, M., Bouchiha, F., Elmaataoui, S., Kharbouche, H. A., Belkoura, I., Naciri, R., Koussa, T., & Mazri, M. A. (2026) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-026-03404-3 · Cited by 1 · see citing works

Epigenetic regulation of plant regeneration and its implications for somaclonal variation and genetic stability

Bharti, M., Shrishti, & Mukherjee, P. (2026) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-026-10697-8

The increase in in vitro shoot multiplication rate of Dendrocalamus asper (Schult. f.) Back. ex Heyne.

Tuấn, T. T., Tu, H. L. T., Giáp, Đ. Đ., & Du, T. X. (2012) · TAP CHI SINH HOC · doi:10.15625/0866-7160/v34n3se.1790 · Cited by 4 · see citing works

Micropropagation of Dendrocalamus asper {Schult. & Schult. F.} Backer ex k. Heyne): an exotic edible bamboo

Singh, S. R., Dalal, S., Singh, R., Dhawan, A. K., & Kalia, R. K. (2011) · Journal of Plant Biochemistry and Biotechnology · doi:10.1007/s13562-011-0095-9 · Cited by 49 · see citing works

Arrangement of cluster and individualized culms affect efficiency in the micropropagation of the bamboo Dendrocalamus asper (Schult. & Schult. f.) Backer ex K. Heyne

Rigo, G., Ornellas, T. S., Serrano, F. S. M., Bastos, F. E. A., Guerra, M. P., & Pescador, R. (2026) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-026-10689-8

In vitro micropropagations of Dendrocalamus asper (Schultes F.) Backer ex Heyne through single node bud culture

Ruhiyat, M., & Gunawan, L. W. (2010)

Rapid Micropropagation of Edible BambooDendrocalamus asper

Arya, I. D., Satsangi, R., & Arya, S. (2001) · Journal of Sustainable Forestry · doi:10.1300/j091v14n02_06 · Cited by 28 · see citing works