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Rapid multiple shoot production from cotyledonary node explants of pea (Pisum sativum L.)

https://doi.org/10.1007/bf02623626
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf00269257openalex-snapshot
Plant regeneration by organogenesis in Glycine max
inferredcites →https://doi.org/10.1007/bf00269274openalex-snapshot
Regeneration of pea (Pisum sativum L. cv. Century) plants by in vitro culture of immature leaflets
inferredcites →https://doi.org/10.1007/bf00272005openalex-snapshot
Plant regeneration via somatic embryogenesis in pea (Pisum sativum L.)
inferredcites →https://doi.org/10.1007/bf00272533openalex-snapshot
Improved protoplast culture and regeneration of shoots in pea (Pisum sativum L.)
inferredcites →https://doi.org/10.1007/bf00274128openalex-snapshot
Specificity of strain and genotype in the susceptibility of pea to Agrobacterium tumefaciens
inferredcites →https://doi.org/10.1007/bf00388239openalex-snapshot
Regeneration of whole plants from callus culture of diverse genetic lines of Pisum sativum L.
inferredcites →https://doi.org/10.1007/bf00716664openalex-snapshot
Transformation of pea (Pisum sativum L.) byAgrobacterium tumefaciens
inferredcites →https://doi.org/10.1007/bf02079328openalex-snapshot
Transformation of meristematic cells in the shoot apex of cultured pea shoots byAgrobacterium tumefaciens andA. rhizogenes
inferredcites →https://doi.org/10.1007/bf02623570openalex-snapshot
Protoplast regeneration and organogenesis from pea protoplasts
inferredcites →https://doi.org/10.1016/0014-4827(68)90403-5openalex-snapshot
Nutrient requirements of suspension cultures of soybean root cells
inferredcites →https://doi.org/10.1016/0168-9452(89)90051-4openalex-snapshot
Regeneration of dry bean (Phaseolus vulgaris L.) via organogenesis
inferredcites →https://doi.org/10.1016/0304-4211(80)90084-xopenalex-snapshot
Plant regeneration from soybean cotyledonary node segments in culture
inferredcites →https://doi.org/10.1016/0304-4211(84)90217-7openalex-snapshot
Plant production in pea (Pisum sativum L. cvs. Puget and Upton) from long-term callus with superficial meristems
inferredcites →https://doi.org/10.1016/s0044-328x(74)80127-3openalex-snapshot
Regeneration of pea (Pisum sativum L.) plants from shoot apical meristems
inferredcites →https://doi.org/10.1016/s0176-1617(84)80024-3openalex-snapshot
Plant Regeneration from Pea Leaflets Cultured in vitro and Genetic Stability of Regenerants
inferredcites →https://doi.org/10.1111/j.1399-3054.1962.tb08052.xopenalex-snapshot
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
inferredcites →https://doi.org/10.1111/j.1399-3054.1974.tb05003.xopenalex-snapshot
Organogenesis in Callus from Shoot Apices of Pisum sativum

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Status and Prospects of Genetic Improvement of Grain Legumes Using in Vitro Techniques: A Review
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Breeding Strategies of Garden Pea (Pisum sativum L.)
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Selection of Elites and In Vitro Propagation of Selected High-Value Himalayan Medicinal Herbs for Sustainable Utilization and Conservation
inferred← citeshttps://doi.org/10.1007/bf00029716openalex-snapshot
Efficient adventitious shoot regeneration and somatic embryogenesis in pea
inferred← citeshttps://doi.org/10.1007/bf00232172openalex-snapshot
Somatic embryogenesis and shoot regeneration from intact seedlings of Phaseolus acutifolius A., P. aureus (L.) Wilczek, P. coccineus L., and P. wrightii L.
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Agrobacterium tumefaciens-mediated beta-glucuronidase (GUS) gene expression in lentil (Lens culinaris Medik.) tissues
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In vitro regeneration of plants: A novel approach
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In vitro induction of multiple shoots and plant regeneration in cotton (Gossypium hirsutum L.)
inferred← citeshttps://doi.org/10.1007/bf01690247openalex-snapshot
Thidiazuron-induced high frequency of shoot induction and plant regeneration in protoplast derived pea callus
inferred← citeshttps://doi.org/10.1007/bf02318979openalex-snapshot
Multiple shoot formation from cotyledonary node segments of Eastern redbud
inferred← citeshttps://doi.org/10.1007/bf02632256openalex-snapshot
Evaluation of a cotyledonary node regeneration system forAgrobacterium-mediated transformation of pea (Pisum sativum L.)
inferred← citeshttps://doi.org/10.1007/bf02782460openalex-snapshot
Transformation of lentil (Lens culinaris M.) cotyledonary nodes by vacuum infiltration ofAgrobacterium tumefaciens
inferred← citeshttps://doi.org/10.1007/bf03321916openalex-snapshot
Simple and Effective Regeneration of Mungbean (Vigna radiata (L) Wilczek) using Cotyledonary Node Explants
inferred← citeshttps://doi.org/10.1007/s10535-005-0009-6openalex-snapshot
Agrobacterium-mediated transformation of Pisum sativum in vitro and in vivo
inferred← citeshttps://doi.org/10.1007/s11240-016-1085-3openalex-snapshot
Optimization of Agrobacterium-mediated genetic transformation of shoot tip explants of green gram (Vigna radiata (L.) Wilczek)
inferred← citeshttps://doi.org/10.1007/s11240-016-1095-1openalex-snapshot
Direct organogenesis from cotyledonary node explants suitable for Agrobacterium-mediated transformation in peanut (Arachis hypogaea L.)
inferred← citeshttps://doi.org/10.1007/s11240-019-01699-zopenalex-snapshot
The influential role of polyamines on the in vitro regeneration of pea (Pisum sativum L.) and genetic fidelity assessment by SCoT and RAPD markers
inferred← citeshttps://doi.org/10.1007/s11627-000-0035-1openalex-snapshot
The growth regulators used for bud regeneration and shoot rooting affect the competence for flowering and seed set in regenerated plants of protein peas
inferred← citeshttps://doi.org/10.1007/s11627-000-0074-7openalex-snapshot
Shoot regeneration from seedling explants of Acacia mangium Willd
inferred← citeshttps://doi.org/10.1007/s11627-000-0090-7openalex-snapshot
Influence of explants, genotypes and culture vessels on sprouting and proliferation of pre-existing meristems of cotton (Gossypium hirsutum L. and Gossypium arboreum L.)
inferred← citeshttps://doi.org/10.1007/s13562-013-0200-3openalex-snapshot
An efficient in vitro regeneration system of fieldpea (Pisum sativum L.) via. shoot organogenesis
inferred← citeshttps://doi.org/10.1007/s13562-016-0354-xopenalex-snapshot
Development of an efficient, genotype independent plant regeneration and transformation protocol using cotyledonary nodes in safflower (Carthamus tinctorius L.)
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Genetic Transformation
inferred← citeshttps://doi.org/10.1023/a:1006325327624openalex-snapshot
Differences in shoot regeneration response from cotyledonary node explants in Asiatic Vigna species support genomic grouping within subgenus Ceratotropis (Piper) Verdc.
inferred← citeshttps://doi.org/10.1023/a:1013874902530openalex-snapshot
Direct shoot regeneration from cotyledonary nodes as a marker for genomic groupings within the Asiatic Vigna (subgenus Ceratotropis {Piper} Verdc.) species
inferred← citeshttps://doi.org/10.1023/a:1024807426591openalex-snapshot
Thidiazuron Induced Multiple Shoot Induction and Plant Regeneration from Cotyledonary Explants of Mulberry
inferred← citeshttps://doi.org/10.1071/fp13191openalex-snapshot
Functional genomics to study stress responses in crop legumes: progress and prospects
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Regeneration of pea (Pisum Sativuml.) by the thin cell layer nodal system: Influence of explant culture media on rooting and plantlet formation
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In vitro studies on Pea (Pisum sativum L.): I. Callus formation, regeneration and rooting
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Protoplast isolation, culture and regeneration from Egyptian cultures of Pea and Beans
inferred← citeshttps://doi.org/10.1104/pp.101.3.751openalex-snapshot
Transformation and Regeneration of Two Cultivars of Pea (Pisum sativum L.)
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Somatic embryogenesis in pea (Pisum sativum L.): effect of explant, genotype and culture conditions
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Potential, constraints and applications of in vitro methods in improving grain legumes
inferred← citeshttps://doi.org/10.1186/s13007-025-01468-4openalex-snapshot
Genotype-independent de novo regeneration protocol in Cannabis sativa L. through direct organogenesis from cotyledonary nodes
inferred← citeshttps://doi.org/10.1186/s40529-014-0045-7openalex-snapshot
In vitro propagation and analysis of secondary metabolites in Glossogyne tenuifolia (Hsiang-Ju) - a medicinal plant native to Taiwan
inferred← citeshttps://doi.org/10.1186/s40529-014-0056-4openalex-snapshot
In vitro propagation of Gentiana scabra Bunge – an important medicinal plant in the Chinese system of medicines
inferred← citeshttps://doi.org/10.1201/9781439801352-24openalex-snapshot
Cotyledonary Node and Embryo Axes as Explants in Legume Transformation with Special Reference to Peanut
inferred← citeshttps://doi.org/10.1201/9781439801352.ch17openalex-snapshot
Cotyledonary Node and Embryo Axes as Explants Legume Transformation with Special Reference to Peanut
inferred← citeshttps://doi.org/10.1270/jsbbs.51.137openalex-snapshot
Benzyladenine-preconditioning in Germinating Mungbean Seedlings Stimulates Axillary Buds in Cotyledonary Nodes Resulting in Multiple Shoot Regeneration.
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Light and Scanning Electron Microscopic Analysis of Benzyl Adenine Induced Multiple Shoot Regeneration in Kenaf (Hibiscus cannabinus L.)
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SILVER NITRATE (AgNO3) BOOSTED HIGH-FREQUENCY MULTIPLE SHOOT REGENERATION FROM COTYLEDONARY NODE EXPLANTS OF OKRA (ABELMOSCHUS ESCULENTUS L.)
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Ultrastructural analysis of in vitro direct and indirect organogenesis
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Efeito do tiadiazuron na micropropagação in vitro de dois genótipos de mamona via organogênese
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Estimation of Outcrossing in Basil
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Micropropagation of Lupinus texensis from Cotyledonary Node Explants
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Plant Regeneration from in Vitro Culture of Embryonic Axis Explants in Common and Tepary Beans
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Dark Preconditioning, CPPU, and Thidiazuron Promote Shoot Organogenesis on Seedling Node Explants of Common and Faba Beans
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Enhanced in vitro shoot proliferation through nodal explants of Staurogyne repens (Nees) Kuntze
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Organogenesis and long-term micropropagatlon of Polish pea cultivars
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