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  • tissue culture  (32)
  • Springer  (32)
  • Cambridge University Press
  • Cell Press
  • 2020-2024
  • 1985-1989  (32)
  • 1960-1964
  • 1950-1954
  • 1988  (32)
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  • 2020-2024
  • 1985-1989  (32)
  • 1960-1964
  • 1950-1954
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  • 1
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    Springer
    Methods in cell science 11 (1988), S. 31-33 
    ISSN: 1573-0603
    Keywords: tissue culture ; flask opening
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A device has been designed to open tissue culture flasks, which is quick and permits easy access for cell cloning, the removal of complete cell sheets, and staining for microscopy. The brass blade used melts the plastic rather than burning, thus reducing the level of potentially toxic fumes produced by some other methods.
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  • 2
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    Journal of chemical ecology 14 (1988), S. 589-603 
    ISSN: 1573-1561
    Keywords: Kalanchöe daigremontiana ; triacontanol ; ferulate esters ; ferulic acid ; tissue culture ; allelopathy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Ferulate esters of normal C22–C30 alcohols were found in the root extract ofKalanchöe daigremontiana and the freen-C30 alcohol, triacontanol, was found on the leaves. Ferulic acid was isolated from the vermiculite in which plants were grown. Whole plant and tissue culture experiments were done to investigate the role of ferulic acid as an allelochemical and of triacontanol as a plant growth regulator inK. daigremontiana and other bioassay systems. No positive growth responses to triacontanol were observed, but inhibitation of growth response of plantlets by ferulic acid was seen.
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  • 3
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    Plant molecular biology 11 (1988), S. 139-145 
    ISSN: 1573-5028
    Keywords: Lycopersicon esculentum Mill. ; ribosomal DNA ; Solanum lycopersicoides Dun. ; somatic hybrid ; tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Restriction fragment polymorphisms were used to identify and quantify the nuclear contributions from each parent to somatic hybrid plants between tomato (Lycopersicon esculentum Mill.) cv. Sub-Arctic Maxi and Solanum lycopersicoides Dun. Three single-copy clones, 2–13, 2–17, and 3–288, and a clone for the 45s ribosomal RNA, pHA2, all mapped to chromosome 2 of tomato, were used in analysis of 47 somatic hybrids. The amount of hybridizing probe for each parental band was quantified by densitometry of the autoradiograph film. Analyses with the three single-copy clones indicated that there were more than two S. lycopersicoides copies in most somatic hybrid plants. For at least one somatic hybrid there was a loss of one tomato copy. No evidence was found for more than two copies donated from tomato or loss of a copy from S. lycopersicoides. Most of the observed variation in copy number of the single-copy clones was consistent with chromosomal changes occurring in the suspension cells from which S. lycopersicoides parental protoplasts were derived. The number of copies of rDNA derived from each parent varied independently of the number of copies of single-copy clones from each parent. Changes in the copy number of rDNA occurred in both tomato and S. lycopersicoides genomes.
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  • 4
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    Cytotechnology 1 (1988), S. 199-214 
    ISSN: 1573-0778
    Keywords: animal cells ; growth factors ; mammalian cells ; media ; serum ; tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The increasing interest in products from animal cells has caused an extensive research effort towards development of media for cell cultivation. The basic components in the media used for cultivation of animal cells vary depending upon the characters of the cells and the cultivation method. Basic components consist of an energy source, nitrogen source, vitamins, fats and fatty soluble components, inorganic salts, nucleic acid precursors, antibiotics, oxygen, pH buffering systems, hormones, growth factors and serum. Extensive efforts are directed towards developing serum-free or chemically defined media. Among the serum substitutes is a long list of hormones and growth factors.
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  • 5
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    Bulletin of experimental biology and medicine 105 (1988), S. 248-250 
    ISSN: 1573-8221
    Keywords: human embryo ; liver ; hepatocytes ; tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
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  • 6
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    Bulletin of experimental biology and medicine 106 (1988), S. 1781-1785 
    ISSN: 1573-8221
    Keywords: leprosy ; tissue culture ; morphology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
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  • 7
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    Cellular and molecular neurobiology 8 (1988), S. 393-410 
    ISSN: 1573-6830
    Keywords: acetylcholine (ACh) receptor ; desensitization ; membrane potential ; skeletal muscle ; tissue culture ; Na-K pump ; carbamylcholine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. We measured changes in resting membrane potential (E m) and Na-K pump activity, assayed by ouabain-sensitive86Rb uptake, in response to carbamycholine (CCh) and its continued presence in single rat skeletal myotubes in culture. 2. CCh caused immediate depolarization from controlE m (-80 to -85 mV) to near 0 followed by repolarization of varying degrees depending on the age of the culture and temperature of the recording medium; repolarization ofE m was most apparent by culture age 8–9 daysin vitro (DIV),E m reaching values as high as -60 mV by 5–10 min after peak depolarization at 37°C. 3. Input resistance, which decreased during CCh depolarization, increased only slightly during the initial phase of repolarization and then remained essentially unchanged during the major component of membrane repolarization in the presence of CCh. 4. Ouabain, given before CCh, prevented repolarization ofE m and, when given after repolarization had begun, reversed it and causedE m to return to about -7 mV. 5. Na-K pump activity was decreased in myotubes in whichE m did not repolarize or did so only slightly, and was increased by over 40–50% in myotubes whoseE m repolarized by 40–60 mV, even though CCh was still present in the medium. Inhibition of pump activity in non repolarizing myotubes was related to Na influx, inhibition being reversed to stimulation when CCh was administered to myotubes in Na-free medium. 6. Repeated (three or four times) or prolonged (up to 60-min) administration of CCh to myotubes in which repolarization was hardly expressed (age 6–7 DIV) caused increases both in the amount of repolarization and in86Rb uptake, both being related to the number or duration of CCh exposures. 7. We conclude that repolarization ofE m following CCh-induced depolarization of cultured rat skeletal myotubes depends to a large extent on an increase in activity of the electrogenic Na-K pump.
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  • 8
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    Euphytica 37 (1988), S. 83-88 
    ISSN: 1573-5060
    Keywords: Brassica ; oilseed crops ; tissue culture ; interspecific hybridization ; biotechnology ; genetic variability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Ovary culture has been employed for the production of interspecific hybrids of a partially compatible cross of Brassica juncea (2n=36) × Brassica campestris (2n=20). Five to seven days old ovaries cultured on White's medium supplemented with casein hydrolysate (300 mg/l) and sucrose (5%) produced more seeds than any other media tried, but seed development was better on media fortified with plant hormones. The seed yield was better in B. juncea × B. campestris than their reciprocal cross. The plants obtained from ovary-derived seeds were transferred to the field; they were intermediate in some morphological characters and chromosome number (2n=28) as compared to their parents. The flower buds generally did not open and had poorly developed anthers with mostly sterile pollen. The pod size/setting was very much reduced, but healthy seeds were obtained.
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  • 9
    ISSN: 1573-5044
    Keywords: Bothriochloa ischaemum ; Cynodon dactylon ; forage grasses ; auxin ; tissue culture ; somatic embryogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Objectives of this research were to test the effects of plant genotypes and auxin 2,4-D (2,4-dichlorophenoxyacetic acid) medium concentrations on embryogenic (E) callus production of two grass species. Two Old World bluestem,Bothriochloa ischaemum, accessions (A-8793 and A-8911c) and three bermudagrass,Cynodon dactylon (L.) Pers., accessions (A-10978b, A12164, and ‘Brazos’) supplied the explant material. Immature inflorescences ≤9 mm in length were placed on modified Murashige-Skoog (MS) agar medium containing 0, 1, 3, or 5 mg L-1 of 2,4-D. Explants of all genotypes produced callus by the end of a 4-week dark incubation period at 25°C. When subcultured onto fresh media and maintained at 25°C with a 16 hr photoperiod, calli became embryogenic within 8 weeks of inoculation. Three mg L-1 of 2,4-D in the media maximized E callus production in both bluestem genotypes and in A-10978b and A-12164 bermudagrass genotypes. Maximum E callus production from Brazos bermudagrass resulted from the 1 mg L-1 treatment. Somatic embryos developed after subculture under light. Embryos showed scutellum-like structures and coleoptile-coleorhiza bipolar organization. Plantlets were regenerated from all genotypes except Brazos, whose embryoids failed to germinate. All callus from Brazos eventually senesced. Light and scanning electron microscopy confirmed regeneration through somatic embryogenesis.
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  • 10
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    Plant cell, tissue and organ culture 12 (1988), S. 235-241 
    ISSN: 1573-5044
    Keywords: tissue culture ; callus ; organogenesis ; strawberry ; somacloning
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Shoots were regenerated from callus of the commercially important strawberry varieties Bogota, Brighton, Cambridge Favourite, Hapil, Ostara, Rapella, Red Gauntlet and JILA33 which is a promising selection from a current breeding programme. The callus was initiated from explants of petiole or lamina of leaves of micropropagated shoots in vitro or of lamina or peduncle from greenhouse plants. There was more shoot regeneration with callus from lamina than from petiole although with the variety Hapil, regeneration occurred only with callus from peduncle. With seven of the varieties, shoot regeneration occurred on culture media with BAP and 2,4-D whilst with the remaining variety, Cambridge Favourite, it occurred only with medium which contained 1AA-β alanine conjugate in place of 2,4-D. Regenerated shoots rooted readily and the plants produced are being studied for somaclonal variation.
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  • 11
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    Plant cell, tissue and organ culture 12 (1988), S. 311-314 
    ISSN: 1573-5044
    Keywords: Oryza sativa ; rice ; tissue culture ; callus growth ; genotype
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A total of 108 rice varieties were examined for their tissue culture responses. Callus tissues were initiated from the seed, radicle, coleoptile and anther explants. Our results indicated that genotypes differed in the ability to develop vigorously growing callus. The callus growth responses in seed, radicle and coleoptile cultures were intercorrelated, but were not correlated with that in anther culture.
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  • 12
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    Plant cell, tissue and organ culture 13 (1988), S. 77-83 
    ISSN: 1573-5044
    Keywords: Dalbergia latifolia ; plant regeneration ; tissue culture ; mass multiplication
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A successful procedure was established for in vitro mass multiplication of Indian rosewood (Dalbergia latifolia Roxb.). In vitro regeneration of plantlets was achieved from callus of shoot tips and shoot segments of over 50-year-old ‘elite’ trees on Murashige & Skoog's medium containing naphthaleneacetic acid (NAA) and benzylaminopurine (BAP). For rooting, regenerated shoots from the calli were excised and first treated with White's liquid medium or half-strength Murashige & Skoog's medium, supplemented with indole-3-acetic acid, indole-3-butyric acid and naphthaleneacetic acid for 48 h to 72 h. Following this treatment, plantlets were transferred to hormone-free half-strength MS medium. Rooted plantlets were then transferred to pots and grown in the greenhouse.
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  • 13
    ISSN: 1573-5044
    Keywords: maize ; Zea ; amino acid analogs ; selection ; tissue culture ; plant regeneration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Tissues resistant to lethal levels of equimolar L-lysine plus L-threonine (LT), 5-methyl-DL-tryptophan (5MT, a tryptophan analog), or S-2-aminoethyl-L-cysteine (AEC, a lysine analog) were selected from maize callus capable of plant regeneration (H99 and W77-R3019 genotypes). Resistance to LT resulted from resistant calli having a 19 times greater level of free threonine than wild type tissues. The resistance was expressed in roots of whole plants; threonine levels were two to nine times greater in leaves and kernels of resistant plants than in wild type plants. Slightly greater levels of isoleucine, lysine and methionine were also noted, particularly in the kernel. Genetic studies with individual resistant plants did not always produce inheritance ratios typical of simple Mendelian inheritance, but by the third generation after plant regeneration a trend towards homozygosity was apparent and the data suggests that LT resistance is inherited as a single dominant nuclear gene. Resistance to 5MT resulted from resistant calli having a 133 to 161 times greater level of free tryptophan than wild type tissues. Also, phenylalanine was 22 to 30 times as great and histidine, tyrosine and valine were about two times as great as in wild type tissues. Resistance was expressed in roots of whole plants, and tryptophan levels were at least 2000 times greater in resistant than in wild type plants. Phenylalanine was also 32 times greater. All regenerant plants resistant to 5MT were both male and female sterile. Resistance to AFC was caused by decreased AEC uptake by the callus tissue and was not due to increased levels of free lysine. Plants were not regenerated from this callus.
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  • 14
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    Plant cell, tissue and organ culture 14 (1988), S. 31-40 
    ISSN: 1573-5044
    Keywords: tissue culture ; Malus domestica ; micropropagation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Shoot tips of ‘York’ and ‘Vermont Spur Delicious’ apples (Malus domestica Borkh.) were cultured in vitro to test the influence of K+, Mg++ and gelling agent concentrations on vitrification. These concentrations were 20.05, 14.05 and 8.05 mM K+, 1.5 and 3.0 mM Mg++, 7.0 g/l Difco Bacto agar and 1.0, 1.5 and 2.0 g/l Gelrite. The lowest K+ level produced a higher percentage of vitrified shoots, affected tissue appearance, reduced shoot number and shoot elongation and apparently altered shoot metabolic activity. Gelrite consistently produced vitrified leaves and stems, even though media gelled with 1.5 g/l Gelrite presented the same apparent gel firmness as using 7 g/l Difco Bacto agar, which did not induce vitrification. Less shoot elongation, fewer total shoots, and more usable shoots of ‘York’ were obtained on Bacto-agar, while similar but less noticeable effects were obtained with ‘Vermont Spur Delicious’. The results presented here show that vitrification can be studied in a standardized system in which the only change is substitution of one gelling agent for another.
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  • 15
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    Plant cell, tissue and organ culture 14 (1988), S. 137-160 
    ISSN: 1573-5044
    Keywords: conifers ; tissue culture ; micropropagation ; adventitious rooting ; acclimatization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Rooting and acclimatization procedures for micropropagated conifers are reviewed, with emphasis on their effects on root quality and plantlet performance in the nursery and field. Major influences on root production include auxin concentration and mode of application, shoot quality, donor age, clone and temperature. The development of a fibrous, well-branched root system has been a problem that may be solved by using rooting substrates that are better-aerated than agar. Further development of the root system may be enhanced by early air-pruning and ectomycorrhizal associations. During acclimatization, high humidity is required for conifers. However, conifers have an advantage over non-coniferous plantlets with respect to water loss because of a better development of the needle cuticles prior to transfer to in vivo conditions. In greenhouse and field comparisons with seedlings, plantlets were similar in survival and growth rate, but root systems were less fibrous. Also, features of early maturation have been observed for plantlets, the cause of which is uncertain. Pertinent research with rooted cuttings and seedlings of conifers has been cited to gain a better understanding of the factors involved in root production and development.
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  • 16
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    Plant cell, tissue and organ culture 14 (1988), S. 161-168 
    ISSN: 1573-5044
    Keywords: Beta vulgaris ; sugarbeet ; cryopreservation ; tissue culture ; germplasm storage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Meristems aseptically isolated from shoots developed on sugarbeet (Beta vulgaris L.) inflorescences were precultured on modified MS agar medium containing 19.4 μM 6-benzylaminopurine, 6 μM triiodobenzoic acid, and supplemented with 5% DMSO. After two days the meristems were transferred to liquid modified MS medium and the cryoprotectants sorbitol and DMSO added in varying concentrations. The meristems were frozen to −40°C and stored in liquid nitrogen. Growth resumed when the meristems were quick-thawed at 39°C.
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  • 17
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    Plant cell, tissue and organ culture 15 (1988), S. 33-45 
    ISSN: 1573-5044
    Keywords: somatic embryogenesis ; tissue culture ; histology ; Trifolium ; zygotic embryogenesis ; regeneration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The origin and development of zygotic and somatic embryos of Trifolium rubens L. was studied with the aid of paraffin sections and light microscopy. Zygotic embryos were collected, fixed and prepared daily from one to ten days after cross-pollination. Somatic embryos were obtained by plating petiole sections on modified L2 medium with 0.015 mgl-1 picloram and 0.1 mgl-1 6-BAP. Cultured petioles were collected and fixed daily from one to 25 days after plating. Two regions in the vascular bundle sheath of cultured petioles gave rise to callus. The first region was adjacent to the phloem fibers and produced friable callus. The second region gave rise to compact callus that was connected to the fascicular cambium. Somatic embryos originated from single cells in the cortex directly without intervening callus formation and from single cells in the friable callus. In addition, embryos arose from meristematic regions in compact callus. Many early stages of embryogenesis (one, two and four-celled stages) were observed in the cortex and friable callus. Zygotic embryogenesis in Trifolium differs from other legumes in that the suspensor is short and has a broad attachment. This arrangement was observed in zygotic embryos of T. rubens and in many somatic embryos. However, a continuum of somatic embryogenesis was observed where some young embryos had a Trifolium suspensor-like arrangement while others were attached to a long narrow suspensor-like structure more characteristic of Medicago.
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  • 18
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    Plant cell, tissue and organ culture 15 (1988), S. 67-71 
    ISSN: 1573-5044
    Keywords: minimum-growth storage ; cold storage ; silicone ; low temperature ; Vitis ; tissue culture ; regeneration ; somatic embryogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Effects of the combination of low temperature and silicone treatment on the storage of grape callus (Vitis vinifera L. x V. labrusca L. cv. Kyoho; V. vinifera L. cv. Koshusanjaku) were examined. In ‘Kyoho’, the calli were stored at 10°C successfully for up to 360 days. Embryogenic calli of ‘Koshusanjaku’ stored at 10°C retained the ability of embryogenesis after 360 days of storage. However, the color of both calli became brownish. This was improved by the combination of low temperature and silicone treatment. The calli of ‘Kyoho’ survived by the storage under the combination of 15°C and silicone. Embryogenic calli stored at 10 and 15°C in combination with silicone survived for 360 days, and regenerated only after transfer onto a regeneration medium. Thus the combination of low temperature and silicone affects the longevity of the grape callus.
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  • 19
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    Plant cell, tissue and organ culture 15 (1988), S. 95-105 
    ISSN: 1573-5044
    Keywords: Populus nigra × P. maximowiczii ; tissue culture ; punctured leaf ; morphogenetic response
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Various explant sources of Populus nigra × P. maximowiczii were used to examine the effects of growth hormones on morphogenesis in vitro. Initial experiments indicated that punctured leaves were superior to non-punctured ones for both callus growth and formation of shoots and roots on MS medium containing various types and concentrations of growth hormones. After 6 weeks in culture, an average of 178 shoots, 129 roots and 3.1 g fresh weight of callus were directly produced from the abaxial side of each punctured leaf. The best combinations of growth hormones for shoot, root and callus proliferation were 0.88 μM BA plus 0.05 μM 2,4-D, 0.44 μM BA plus 2.69 μM NAA and 0.44 μM BA plus 2.26 μM 2,4-D, respectively. Embryoids were also formed on callus derived from punctured leaves. The number of embryoids varied from 0 to 30 per punctured leaf. Adventitious shoots also developed simultaneously with the embryos. Embryoids were removed with a scalpel at the early developmental stages and placed on MS medium lacking growth regulators. Regenerated plantlets were transferred to pots containing vermiculite for normal growth in the greenhouse.
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  • 20
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    Plant cell, tissue and organ culture 15 (1988), S. 107-111 
    ISSN: 1573-5044
    Keywords: Brassica tournefortii ; tissue culture ; regeneration ; micropropagation ; organogenesis in vitro
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cotyledon explants of Brassica tournefortii L. were excised from germinated seedlings and cultured on Murashige & Skoog's [6] basal medium supplemented with various combinations of cytokinins and auxins, Both cytokinin and auxin were required for induction of shoot organogenesis. Of the three cytokinins tested (in combination with a low concentration of IAA), kinetin was found to be the best for shoot regeneration. On this medium, cotyledonary explants invariably underwent callusing followed by multiple shoot formation. NAA in combination with any of the three cytokinins yielded a reduced number of shoots or none, but favoured good callus growth. Callus so produced also regenerated shoots when subcultured on media containing high concentration of KIN or ZEA and low concentration of IAA. Shoots were rooted during prolonged incubation on the same medium or on MS medium free of growth regulators. Mature plants were grown in the greenhouse.
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  • 21
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    Plant cell, tissue and organ culture 15 (1988), S. 161-167 
    ISSN: 1573-5044
    Keywords: Cyphomandra betacea ; somatic embryogenesis ; plant regeneration ; tissue culture ; growth regulators
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Callus cultures with globular proembryogenic structures were induced from zygotic embryos and hypocotyl segments of Cyphomandra betacea on MS medium supplemented with 2,4-D. Proembryogenic structures produced somatic embryos and plantlets on regulator-free basal medium. Pieces of embryogenic callus subcultured on medium with the same original composition gave rise to new globular structures and the potential for plantlet regeneration has been maintained for over a year. The histological examination of these proembryogenic structures suggested that somatic embryos arise from single cells. Regenerated plants are phenotypically normal, having diploid chromosome numbers (2n = 24).
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  • 22
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    Plant cell, tissue and organ culture 15 (1988), S. 183-187 
    ISSN: 1573-5044
    Keywords: tissue culture ; morphogenesis ; suspension culture ; garlic ; Allium sativum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Rapidly growing, regenerable suspension cultures were obtained from meristem-derived callus cultures of garlic (Allium sativum L.). The liquid culture medium consisted of MS salts, B5 vitamins, 3% sucrose, 1 mg l−1 naphthalene-acetic acid (NAA) and 2 mg l−1 6-benzyladenine (BA). The tissue in the suspension culture was yellow, smooth, organized, and proliferated as nodular clumps. Histological examination revealed that these morphogenic clumps had a well-defined epidermis. Following transfer of the morphogenic clumps to an agar-solidified medium, numerous meristems with green leaf primordia were produced.
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  • 23
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    Plant cell, tissue and organ culture 15 (1988), S. 189-199 
    ISSN: 1573-5044
    Keywords: tissue culture ; Hippophae rhamnoides ; Frankia ; actinorhizal ; in vitro ; nitrogen fixation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Micropropagation of the actinorhizal plant Hippophae rhamnoides L. (sea-buckthorn) was achieved on Murashige and Skoog (MS) medium supplemented with 1 μM of benzylaminopurine (BA). A multiplication frequency of three to five shoots per explant was observed after 28 days. Rooting of these shoots was achieved in a medium containing 1/4 strength MS without growth regulators. The rooted plants were transferred to Turface R artificial substrate and inoculated with pure cultures of two Frankia strains. These plantlets subsequently developed nodules which fixed nitrogen.
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  • 24
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    Plant cell, tissue and organ culture 15 (1988), S. 269-274 
    ISSN: 1573-5044
    Keywords: agar ; Gelrite ; Gossypium hirsutum ; tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A factorial experiment was performed to develop a medium which would support initiation and proliferation of callus in a diverse group of exotic lines of Gossypium hirsutum. Seed hypocotyls of T1, T25 and T133 were cultured on Linsmaier and Skoog (LS) basal medium (1965) with NAA or 2,4-D tested in combination with BA or kinetin. The best medium from this study was then compared to five published media for support of callus initiation and growth of the varieties Acala 1517-75, Coker 500, Dunn 120, Paymaster 303 and TM1. Furthermore, the effects of two gelling agents, Difco-Bacto agar and Kelco Gelrite, were investigated with each of the six media. Significantly more callus was initiated on media solidified with Gelrite than with agar. The best callus production occurred on LS medium supplemented with 30gl-1 glucose, 0.1 mgl-1 BA and 0.1 mgl-1 2,4-D.
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  • 25
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    Methods in cell science 11 (1988), S. 23-26 
    ISSN: 1573-0603
    Keywords: dental pulp ; fibroblasts ; tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A simple, reliable technique for establishing cultures of human pulpal fibroblasts is presented. The technique relies on a sequential digestion of minced pulpal tissue with collagenase and trypsin and produces confluent cultures in 7 to 10 d from four to five pulps.
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  • 26
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    Methods in cell science 11 (1988), S. 129-133 
    ISSN: 1573-0603
    Keywords: endometrium ; fetal ; tissue culture ; bovine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Primary epithelial cell cultures were developed from fetal caruncular, adult intercaruncular pregnant, and adult intercaruncular nonpregnant endometrium. Endometrial cells were obtained from both collagenase dispersion or from explant outgrowth, although the explant method was more consistent. Cultures derived from fetal endometrium grew more rapidly and were more viable after subculturing and cryopreservation than were adult-derived cultures. These cultures provide an in vitro system for the study of bovine endometrial physiology and pathology.
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    Methods in cell science 11 (1988), S. 223-227 
    ISSN: 1573-0603
    Keywords: biosafety ; biohazards ; tissue culture ; containment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A brief description of the need for procedures to provide a safe working environment for cell culture personnel is outlined, and the methods employed at the American Type Culture Collection to achieve this goal are detailed.
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    Methods in cell science 11 (1988), S. 123-128 
    ISSN: 1573-0603
    Keywords: placenta ; trophoblastic cell ; tissue culture ; bovine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Procedures for the isolation and cultivation of bovine cotyledonary trophoblastic cells from early second trimester placentas are described. Collagenase digestion yielded a single cell suspension of both uninucleate and binucleate cells with minimal contamination with other cell types. Optimal growth conditions were obtained through supplementation of medium with epidermal growth factor, insulin, transferrin, and selenium. Trophoblastic cells survived multiple passages, cryopreservation, and serum deprivation and have been maintained in culture for more than 14 mo. Two cell types were identified by phase microscopy: uninucleated trophoblastic cells and trophoblastic giant cells, which were predominantly binucleate cells. Binucleate cells were present in small numbers through all passages. This procedure provides a reliable method to obtain trophoblastic cell lines for studies of trophoblastic cell physiology and susceptibility to infectious and toxic agents.
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    Euphytica 39 (1988), S. 3-9 
    ISSN: 1573-5060
    Keywords: Medicago sativa ; alfalfa ; lucerne ; tissue culture ; callus ; segregation ratio ; complementary genes ; genetic control
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The genetic control of plant regeneration from callus culture was studied in tetraploid alfalfa (Medicago sativa L.). Seven cultivars (total 72 plants) were screened for regenerability. Ladak had the best regeneration response, in which 42% of the plants regenerated. Four regenerable plants and three nonregenerable plants were used to form 10F1 hybrids and three S1 populations. Segregation ratios in the populations suggested that regenerability of alfalfa via petiole culture was under the control of two complementary genes, Rn3 and Rn4. The presence of both dominant genes was necessary for a plant to regenerate in a two-step culture system. The data also indicated that gene dosage influenced regeneration efficiency. Significant reciprocal effects demonstrated that the interaction between callus induction medium and callus regenerability was affected by cytoplasmic factor(s).
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    Cell biology and toxicology 4 (1988), S. 349-356 
    ISSN: 1573-6822
    Keywords: pancreatic islets ; streptozotocin ; Syrian hamster ; tissue culture ; toxicity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Pancreatic islets of the Syrian golden hamster were maintained in culture for extended periods of time. Toxicity of streptozotocin in these cultures was evaluated by measurement of insulin secretion. Exposure of islets to 1 or 2 mM streptozotocin immediately following isolation resulted in a permanent and dose-related inhibition of insulin secretion. This was accompanied by islet disruption as observed by phase-contrast microscopy. Culture of islets for 24 hours before streptozotocin exposure afforded protection from toxicity. For example, exposure of freshly isolated islets to 2 mM streptozotocin resulted in complete destruction of beta cells, whereas islets similarly exposed after a 24 hr culture period continued to secrete insulin for many months. Islets maintained in culture for one week before exposure to 0.1–0.5 mM streptozotocin, however, became more sensitive than freshly isolated islets. Repeated weekly exposure of cultured islets to a “non-toxic” concentration (0.1 mM) resulted in sustained suppression of insulin secretion after 11 weeks.
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    BioControl 33 (1988), S. 261-267 
    ISSN: 1573-8248
    Keywords: Lysiphlebus fabarum ; Aphis fabae ; in vitro rearing ; tissue culture ; endoparasitoids ; Lysiphlebus fabarum ; Aphis fabae ; élevagein vitro ; culture de tissus ; endoparasitoïdes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Description / Table of Contents: Résumé Un essai d'élevagevitro de l'endoparasitoïdeLysiphlebus fabarum (Marshall) a été effectué. La difficulté d'obtenir des cultures cellulaires permanentes d'Aphis fabae. Sc., a orienté les recherches vers l'élevage des larves dans des substrats inhabituels. On a aussi réalisé des essais en utilisant une lignée cellulairein vitro deCeratitis capitata (Wied.). Un groupe de larves a été élevé dans un milieu auquel avaient été ajoutés les tératocites du parasitoïde. Les femelles deLysiphlebus fabarum n'ayant pas pondu dans les capsules de paraffine renfermant le milieu biologique, des larves prélevées dans les aphides parasités y ont été directement transférées. Plusierus larves ont atteint la maturité au cours de mues successives normales, mais seulement deux d'entre elles sur 48 ont donné naissance à des adultes. La significantion des tératocites parasitaires dans l'élevagein vitro, des hyménoptères Braconides est discuté.
    Notes: Abstract In vitro rearing of the aphid endoparasitoidLysiphlebus fabarum (Marshall) (Hymenoptera, Braconidae) was attempted. Successful permanent cultures ofAphis fabae Sc. andMyzus persicae Sulz. cells were not obtained. Therefore, parasitoid larvae were reared in 2 unnatural media rone of which included cells ofCeratitis capitata Wied. (Diptera, Trypetidae). A group of larvae was reared in a substrate to which parasitoid teratocytes had been added. SinceLysiphlebus fabarum females did not oviposit into paraffin droplets including the substrates, the larvae were directly transferred from parasitized aphids into the rearing media. Several larvae reached the final instar, but only 2 out of the 48 tested in the 3 substrates became adults. The meaning of teratocytes inin vitro rearing of Aphidiine, Braconids is discussed.
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    Bulletin of experimental biology and medicine 106 (1988), S. 1477-1479 
    ISSN: 1573-8221
    Keywords: sarcoma virus ; rats ; tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
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