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Status and Prospects of Genetic Improvement of Grain Legumes Using in Vitro Techniques: A Review

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What this work says

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

inferredcites →https://doi.org/10.1002/ps.2780270207openalex-extracted

Potential for exploiting plant genes to genetically engineer insect resistance, exemplified by the cowpea trypsin inhibitor gene

inferredcites →https://doi.org/10.1007/978-3-319-27096-8openalex-extracted

Gene Pool Diversity and Crop Improvement

inferredcites →https://doi.org/10.1007/978-981-13-8499-8_5openalex-extracted

The Model Legume Medicago truncatula: Past, Present, and Future

inferredcites →https://doi.org/10.1007/bf00023889openalex-extracted

Genetic diversity and phylogenetic relationships among the annual Cicer species as revealed by isozyme polymorphism

inferredcites →https://doi.org/10.1007/bf00037796openalex-extracted

In vitro regeneration of chickpea (Cicer arietinum L.): Stimulation of direct organogenesis and somatic embryogenesis by thidiazuron

inferredcites →https://doi.org/10.1007/bf00232818openalex-extracted

Plant regeneration via somatic embryogenesis in chick pea (Cicer arietinum L.)

inferredcites →https://doi.org/10.1007/bf00232946openalex-extracted

Whole plant regeneration of Cicer arietinum from callus cultures via organogenesis

inferredcites →https://doi.org/10.1007/bf00234579openalex-extracted

Crown gall transformation of lentil (Lens culinaris Medik.) with virulent strains of Agrobacterium tumefaciens

inferredcites →https://doi.org/10.1007/bf00235081openalex-extracted

Agrobacterium tumefaciens-mediated beta-glucuronidase (GUS) gene expression in lentil (Lens culinaris Medik.) tissues

inferredcites →https://doi.org/10.1007/bf00237052openalex-extracted

Genetic transformation in the grain legume Cicer arietinum L. (chickpea)

inferredcites →https://doi.org/10.1007/bf01275444openalex-extracted

Efficient transgenic plant regeneration throughAgrobacterium-mediated transformation of Chickpea (Cicer arietinum L.)

inferredcites →https://doi.org/10.1007/bf02623626openalex-extracted

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

inferredcites →https://doi.org/10.1007/bf02672069openalex-extracted

Nuclear DNA content of some important plant species

inferredcites →https://doi.org/10.1007/s00122-002-0930-4openalex-extracted

Identification of an STMS marker for the double-podding gene in chickpea

inferredcites →https://doi.org/10.1007/s00122-008-0944-7openalex-extracted

Mapping QTL for drought stress-induced premature senescence and maturity in cowpea [Vigna unguiculata (L.) Walp.]

inferredcites →https://doi.org/10.1007/s00299-003-0620-yopenalex-extracted

An efficient protocol for shoot regeneration and genetic transformation of pigeonpea [Cajanus cajan (L.) Millsp.] using leaf explants

inferredcites →https://doi.org/10.1007/s00299-003-0640-7openalex-extracted

Influence of Agrobacterium tumefaciens strain on the production of transgenic peas ( Pisum sativum L.)

inferredcites →https://doi.org/10.1007/s00299-003-0730-6openalex-extracted

Use of a herbicide or lysine plus threonine for non-antibiotic selection of transgenic chickpea

inferredcites →https://doi.org/10.1007/s00299-004-0857-0openalex-extracted

Agrobacterium tumefaciens-mediated transformation of chickpea (Cicer arietinum L.): gene integration, expression and inheritance

inferredcites →https://doi.org/10.1007/s00299-008-0606-xopenalex-extracted

Transgenic cowpea (Vigna unguiculata) seeds expressing a bean α-amylase inhibitor 1 confer resistance to storage pests, bruchid beetles

inferredcites →https://doi.org/10.1007/s00299-008-0652-4openalex-extracted

Agrobacterium tumefaciens-mediated genetic transformation of a recalcitrant grain legume, lentil (Lens culinaris Medik)

inferredcites →https://doi.org/10.1007/s00299-013-1385-6openalex-extracted

Development of transgenic imazapyr-tolerant cowpea (Vigna unguiculata)

inferredcites →https://doi.org/10.1007/s00299-014-1699-zopenalex-extracted

DREB1A overexpression in transgenic chickpea alters key traits influencing plant water budget across water regimes

inferredcites →https://doi.org/10.1007/s00299-017-2201-5openalex-extracted

Oil body biogenesis and biotechnology in legume seeds

inferredcites →https://doi.org/10.1007/s002990050005openalex-extracted

Agrobacterium mediated transformation of chickpea ( Cicer arietinum L.) embryo axes

inferredcites →https://doi.org/10.1007/s002990050395openalex-extracted

Plant regeneration via somatic embryogenesis in pigeonpea ( Cajanus cajan L. Millsp)

inferredcites →https://doi.org/10.1007/s00425-010-1173-2openalex-extracted

ROS resistance in Pisum sativum cv. Alaska: the involvement of nucleoside diphosphate kinase in oxidative stress responses via the regulation of antioxidants

inferredcites →https://doi.org/10.1007/s00425-014-2111-5openalex-extracted

VuDREB2A, a novel DREB2-type transcription factor in the drought-tolerant legume cowpea, mediates DRE-dependent expression of stress-responsive genes and confers enhanced drought resistance in transgenic Arabidopsis

inferredcites →https://doi.org/10.1007/s00438-010-0516-9openalex-extracted

Characterization of expressed sequence tags (ESTs) of pigeonpea (Cajanus cajan L.) and functional validation of selected genes for abiotic stress tolerance in Arabidopsis thaliana

inferredcites →https://doi.org/10.1007/s10142-014-0399-7openalex-extracted

The CarERF genes in chickpea (Cicer arietinum L.) and the identification of CarERF116 as abiotic stress responsive transcription factor

inferredcites →https://doi.org/10.1007/s10725-015-0124-0openalex-extracted

A chickpea stress-responsive NAC transcription factor, CarNAC5, confers enhanced tolerance to drought stress in transgenic Arabidopsis

inferredcites →https://doi.org/10.1007/s11032-009-9258-yopenalex-extracted

Genetic engineering of chickpea (Cicer arietinum L.) with the P5CSF129A gene for osmoregulation with implications on drought tolerance

inferredcites →https://doi.org/10.1007/s11105-016-1004-0openalex-extracted

A chickpea NAC-type transcription factor, CarNAC6, confers enhanced dehydration tolerance in Arabidopsis

inferredcites →https://doi.org/10.1007/s11240-007-9227-2openalex-extracted

Increasing lysine levels in pigeonpea (Cajanus cajan (L.) Millsp) seeds through genetic engineering

inferredcites →https://doi.org/10.1007/s11240-008-9443-4openalex-extracted

The effect of cocultivation treatments on transformation efficiency in pea (Pisum sativum L.)

inferredcites →https://doi.org/10.1007/s11240-013-0378-zopenalex-extracted

Expression of the Vigna aconitifolia P5CSF129A gene in transgenic pigeonpea enhances proline accumulation and salt tolerance

inferredcites →https://doi.org/10.1007/s11240-014-0549-6openalex-extracted

Ectopic expression of pigeonpea cold and drought regulatory protein (CcCDR) in yeast and tobacco affords multiple abiotic stress tolerance

inferredcites →https://doi.org/10.1007/s11240-016-1055-9openalex-extracted

Pod borer resistant transgenic pigeon pea (Cajanus cajan L.) expressing cry1Ac transgene generated through simplified Agrobacterium transformation of pricked embryo axes

inferredcites →https://doi.org/10.1007/s11248-009-9242-7openalex-extracted

Tissue specific expression of potent insecticidal, Allium sativum leaf agglutinin (ASAL) in important pulse crop, chickpea (Cicer arietinum L.) to resist the phloem feeding Aphis craccivora

inferredcites →https://doi.org/10.1007/s11627-009-9212-zopenalex-extracted

Effect of TDZ on plant regeneration from mature seeds in pea (Pisum sativum)

inferredcites →https://doi.org/10.1007/s11627-999-0002-4openalex-extracted

Genotypic response of cowpea Vigna unguiculata (L.) to in vitro regeneration from cotyledon explants

inferredcites →https://doi.org/10.1007/s11738-006-0020-3openalex-extracted

The transformation of pea (Pisum sativum L.): applicable methods of Agrobacterium tumefaciens-mediated gene transfer

inferredcites →https://doi.org/10.1007/s12298-008-0030-2openalex-extracted

In planta transformation of pigeon pea: a method to overcome recalcitrancy of the crop to regeneration in vitro

inferredcites →https://doi.org/10.1007/s12298-010-0030-xopenalex-extracted

Agrobacterium-mediated transformation in chickpea (Cicer arietinum L.) with an insecticidal protein gene: optimisation of different factors

inferredcites →https://doi.org/10.1007/s12892-010-0063-2openalex-extracted

Agrobacterium-mediated genetic transformation of pigeon pea [Cajanus cajan (L.) Millsp.] for resistance to legume pod borer Helicoverpa armigera

inferredcites →https://doi.org/10.1016/0168-9452(86)90166-4openalex-extracted

Transformation of cowpea Vigna unguiculata cells with an antibiotic resistance gene using a Ti-plasmid-derived vector

inferredcites →https://doi.org/10.1016/j.ijbiomac.2013.04.055openalex-extracted

Structural and functional studies on urease from pigeon pea (Cajanus cajan)

inferredcites →https://doi.org/10.1016/j.jplph.2007.03.011openalex-extracted

Molecular cloning of glutathione reductase cDNAs and analysis of GR gene expression in cowpea and common bean leaves during recovery from moderate drought stress

inferredcites →https://doi.org/10.1016/j.mrgentox.2007.03.012openalex-extracted

Effects of cadmium on root apical meristems of Pisum sativum L.: Cell viability, cell proliferation and microtubule pattern as suitable markers for assessment of stress pollution

inferredcites →https://doi.org/10.1016/j.plantsci.2003.08.020openalex-extracted

Expression of biologically active Hemagglutinin-neuraminidase protein of Peste des petits ruminants virus in transgenic pigeonpea [Cajanus cajan (L) Millsp.]

inferredcites →https://doi.org/10.1016/j.plantsci.2004.12.015openalex-extracted

Agrobacterium-mediated transformation of chickpea (Cicer arietinum L.) with Bacillus thuringiensis cry1Ac gene for resistance against pod borer insect Helicoverpa armigera

inferredcites →https://doi.org/10.1016/j.plantsci.2006.11.009openalex-extracted

Agrobacterium tumefaciens-mediated high frequency genetic transformation of an Indian cowpea (Vigna unguiculata L. Walp.) cultivar and transmission of transgenes into progeny

inferredcites →https://doi.org/10.1016/j.plaphy.2011.10.008openalex-extracted

Differential expression of antioxidant enzymes and PR-proteins in compatible and incompatible interactions of cowpea (Vigna unguiculata) and the root-knot nematode Meloidogyne incognita

inferredcites →https://doi.org/10.1016/s0168-9452(98)00184-8openalex-extracted

Kanamycin is effective for selecting transformed peas

inferredcites →https://doi.org/10.1017/s0007485312000818openalex-extracted

Resistance of αAI-1 transgenic chickpea (Cicer arietinum) and cowpea (Vigna unguiculata) dry grains to bruchid beetles (Coleoptera: Chrysomelidae)

inferredcites →https://doi.org/10.1023/a:1006060318752openalex-extracted

Thidiazuron-induced shoot regeneration in pigeonpea (Cajanus cajan L.)

inferredcites →https://doi.org/10.1023/a:1022851703409openalex-extracted

Shoot organogenesis and plantlet regeneration from leaf segments of pigeonpea

inferredcites →https://doi.org/10.1039/c0mt00040jopenalex-extracted

A comparative study of element concentrations and binding in transgenic and non-transgenic soybean seeds

inferredcites →https://doi.org/10.1071/cp10351openalex-extracted

Expression of the DREB1A gene in lentil (Lens culinaris Medik. subsp. culinaris) transformed with the Agrobacterium system

inferredcites →https://doi.org/10.1079/ivp2002303openalex-extracted

Production of fertile transgenic lentil (Lens culinaris Medik) plants using particle bombardment

inferredcites →https://doi.org/10.1079/ivp2005730openalex-extracted

Agrobacterium-mediated production of transgenic pigeonpea (Cajanus cajan L. Millsp.) expressing the synthetic BT cry1Ab gene

inferredcites →https://doi.org/10.1080/09670878409370853openalex-extracted

Prevalence of pigeonpea diseases and associated crop losses in Asia, Africa and the Americas∗

inferredcites →https://doi.org/10.1093/jxb/erh198openalex-extracted

Sulphur and nitrogen nutrition influence the response of chickpea seeds to an added, transgenic sink for organic sulphur

inferredcites →https://doi.org/10.1093/jxb/eru224openalex-extracted

Overexpression of pigeonpea stress-induced cold and drought regulatory gene (CcCDR) confers drought, salt, and cold tolerance in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.106.081752openalex-extracted

Expression of CAP2, an APETALA2-Family Transcription Factor from Chickpea, Enhances Growth and Tolerance to Dehydration and Salt Stress in Transgenic Tobacco

inferredcites →https://doi.org/10.1111/j.1365-3040.2010.02151.xopenalex-extracted

Isolation and characterization of a pigeonpea cyclophilin (CcCYP) gene, and its over‐expression in Arabidopsis confers multiple abiotic stress tolerance

inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03169.xopenalex-extracted

Heterotrimeric G‐protein complex and G‐protein‐coupled receptor from a legume ( Pisum sativum ): role in salinity and heat stress and cross‐talk with phospholipase C

inferredcites →https://doi.org/10.1126/science.182.4115.887openalex-extracted

Domestication of Pulses in the Old World

inferredcites →https://doi.org/10.1134/s1021443711040273openalex-extracted

Quantitative analysis of chitinase gene expression in chickpea

inferredcites →https://doi.org/10.1186/1746-4811-8-22openalex-extracted

Use of ex vitro composite plants to study the interaction of cowpea (Vigna unguiculata L.) with the root parasitic angiosperm Striga gesnerioides

inferredcites →https://doi.org/10.1371/journal.pone.0114107openalex-extracted

Genome-Wide Identification and Expression Analysis of the CaNAC Family Members in Chickpea during Development, Dehydration and ABA Treatments

inferredcites →https://doi.org/10.1503/cmaj.131727openalex-extracted

Effect of dietary pulse intake on established therapeutic lipid targets for cardiovascular risk reduction: a systematic review and meta-analysis of randomized controlled trials

inferredcites →https://doi.org/10.2134/agronmonogr52.c10openalex-extracted

Future Biotechnology of Legumes

inferredcites →https://doi.org/10.2307/2258508openalex-extracted

Tropical Crops. Dicotyledons.

inferredcites →https://doi.org/10.4161/gmcr.21897openalex-extracted

Effect of antifungal genes expressed in transgenic pea (Pisum sativum L.) on root colonization with Glomus intraradices

inferredcites →https://doi.org/10.4161/gmcr.28098openalex-extracted

Economic impact of GM crops

inferredcites →https://doi.org/10.4314/ajb.v7i18.59259openalex-extracted

CRY 1AB trangenic cowpea obtained by nodal electroporation

inferredcites →https://doi.org/10.5511/plantbiotechnology.16.213openalex-extracted

Agrobacterium-mediated Genetic Transformation of Pigeonpea (Cajanus cajan L.) and Development of Transgenic Plants via Direct Organoenesis.

inferredcites →https://doi.org/10.5772/66263openalex-extracted

Functional Food - Improve Health through Adequate Food

inferredcites →https://doi.org/10.5897/ajps.9000124openalex-extracted

EXOGENOUS ASCORBIC ACID (VITAMIN C) INDUCED ANABOLIC CHANGES FOR SALT TOLERANCE IN CHICK PEA (CICER ARIETINUM L.) PLANTS

What points at this work

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

inferred← citeshttps://doi.org/10.1007/978-981-19-3627-2_15-1openalex-snapshot

Next-Generation Breeding for Nutritional Traits in Peanut

inferred← citeshttps://doi.org/10.1007/978-981-19-4169-6_15openalex-snapshot

Next-Generation Breeding for Nutritional Traits in Peanut

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