Cited by 676Plant tissue culture and regenerationPlant Genetic and Mutation StudiesBanana Cultivation and Research

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Somaclonal variation in plants: causes and detection methods

Bairu, Michael W., Aremu, Adeyemi O., Van Staden, Johannes·2011·Plant Growth Regulation

DOI 10.1007/s10725-010-9554-x

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DNA polymorphisms amplified by arbitrary primers are useful as genetic markers
Williams, J. G., Kubelik, A. R., Livak, K. J., Rafalski, J. A., & Tingey, S. V. (1990) · Nucleic Acids Research · doi:10.1093/nar/18.22.6531 · Cited by 13,077
AFLP: a new technique for DNA fingerprinting
Vos, P., Hogers, R. C. J., Bleeker, M., Reijans, M., van de Lee, T., Hornes, M., Frijters, A., Pot, J., Paleman, J., Kuiper, M. T. R., et al. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.21.4407 · Cited by 12,405
Construction of a genetic linkage map in man using restriction fragment length polymorphisms.
Botstein, D., White, R. L., Skolnick, M. H., & Davis, R. W. (1980) · Europe PMC (PubMed Central) · Cited by 8,327
Fingerprinting genomes using PCR with arbitrary primers
Welsh, J., & McClelland, M. (1990) · Nucleic Acids Research · doi:10.1093/nar/18.24.7213 · Cited by 5,195
Genome Fingerprinting by Simple Sequence Repeat (SSR)-Anchored Polymerase Chain Reaction Amplification
Ziętkiewicz, E., Rafalski, A. J., & Labuda, D. (1994) · Genomics · doi:10.1006/geno.1994.1151 · Cited by 3,404
Somaclonal variation — a novel source of variability from cell cultures for plant improvement
Larkin, P. J., & Scowcroft, W. R. (1981) · Theoretical and Applied Genetics · doi:10.1007/bf02342540 · Cited by 3,002
Slipped-strand mispairing: a major mechanism for DNA sequence evolution.
Levinson, G., & Gutman, G. A. (1987) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a040442 · Cited by 2,251
Chemical regulation of growth and organ formation in plant tissues cultured in vitro.
Skoog, F. K., & Miller, C. O. (1957) · PubMed · Cited by 2,188
A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene.
Litt, M., & Luty, J. A. (1989) · PubMed · Cited by 1,962
The origin and behavior of mutable loci in maize
McClintock, B. (1950) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.36.6.344 · Cited by 1,752

Show all 313 references

Research works printed but not linked: 9

Bright S, Jarret V, Nelson R, Creissen G, Karp A, Franklin J, Norbury P, Kueh J, Rognes S, Miflin B (1983) Modification of agronomic traits using in vitro technology. In: Mantell SH, Smith H (eds) Plant biotechnology. Cambridge University Press, New York, pp 251–265
El-Sayed OE, Rizkalla AA, Sabri SRS (2007) In vitro mutagenesis for genetic improvement of salinity tolerance in wheat. Res J Agric Biol Sci 4:377–383
Gengenbach BG, Umpeck P (1982) Characteristics of T-cytoplasm revertants from tissue culture. Maize Genet Coop News Lett 56:140–142
Jain SM (1997) Micropropagation of selected somaclones of Begonia and Saintpaulia. J Biosci 22:582–592
Joshi RK, Rao GJN (2009) Somaclonal variation in submergence tolerant rice cultivars and induced diversity evaluation by PCR markers. Int J Genet Mol Biol 1:80–88
Lee YI, Lee IS, Lim YP (2002) Variation in sweetpotato regenerates from gamma-ray irridiated embryogenic callus. J Plant Biotechnol 4:163–170
Mujib A, Banerjee S, Dev Ghosh P (2007) Callus induction, somatic embryogenesis and chromosomal instability in tissue culture-raised hippeastrum (Hippeastrum hybridum cv. United Nations). Propag Ornam Plants 7:169–174
Rivera FN (1983) Protein and isoenzyme banding patterns among Philippine cooking bananas and their wild parents (Musa species). Paradisiaca 6:7–12
Shepherd K, Dos Santos JA (1996) Mitotic instability in banana varieties. I. Plants from callus and shoot tip cultures. Fruits 51:5–11

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Authors: Bairu, M. W., Aremu, A. O., & Van Staden, J.
Affiliations: University of KwaZulu-Natal (ZA)
ORCID: Bairu, Michael W.
Aremu, Adeyemi O.
Venue: Plant Growth Regulation
Publisher: Springer Science and Business Media LLC
Published: 2010-12-25
Volume: 63
Issue: 2
Pages: 147-173
ISSN: 0167-6903 (ISSN-L)
1573-5087
DOI: 10.1007/s10725-010-9554-x
OpenAlex: W2054387047
Cited by: 674
References: 313
Citations by year: 2026: 46 · 2025: 54 · 2024: 46 · 2023: 55 · 2022: 61 · 2021: 67 · 2020: 53 · 2019: 34 · 2018: 47 · 2017: 41 · 2016: 37 · 2015: 41 · 2014: 30 · 2013: 30 · 2012: 23
FWCI: 8.08
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Plant Growth Regulation (publishedVersion)
Funders: National Research Foundation
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant tissue culture and regeneration
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Genetic and Mutation Studies
Life Sciences › Agricultural and Biological Sciences › Plant Science › Banana Cultivation and Research
Keywords: somaclonal variation, plant tissue culture, somaclonal variants, plant breeding, plant conservation

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