Elasmobranch tissue culture: In vitro growth of brain explants from a shark (Rhizoprionodon) and dogfish (Squalus)

1988 ◽  
Vol 20 (5) ◽  
pp. 759-761 ◽  
Author(s):  
William Dean A. Garner
Keyword(s):  
Tissue Culture ◽  
In Vitro Growth ◽  
Culture In Vitro

Metabolism of cells in tissue culture in vitro

1962 ◽  
Vol 26 (1) ◽  
pp. 129-135 ◽  
Author(s):  
J. Michl
Keyword(s):  
Tissue Culture ◽  
Culture In Vitro

Patterns of pigmentation in experimentally produced mouse chimaerae

Development ◽  
1964 ◽  
Vol 12 (4) ◽  
pp. 575-585
Author(s):  
Andrzej K. Tarkowski
Keyword(s):  
Tissue Culture ◽  
Annual Meeting ◽  
Histological Analysis ◽  
Present Report ◽  
General Description ◽  
Tissue Culture Association ◽  
Culture In Vitro ◽  
Pigment Synthesis

A General description of the development of mouse chimaerae and an account of the techniques for their production were given in previous reports (Tarkowski, 1961, 1963). The chimaeric character of the embryos and young obtained was tentatively claimed in the first of these publications because (1) the actual union of two eggs into one blastocyst was seen in culture in vitro, (2) of the occurrence of intersexes, (3) pigment synthesis of the types of the dark component occurred in the majority of individuals developed from pairs of eggs differing genetically in factors for pigmentation. The last criterion was met only by macroscopic search for pigment in the eyes. The present report gives a more detailed description of the distribution of pigment forming cells in these animals, based on histological analysis. Some remarks on the validity and applicability of such a criterion for estimating the degree of chimaerism were made at the 13th Annual Meeting of the Tissue Culture Association (Tarkowski 1963).

Virulence of tissue culture-propagated canine distemper virus

1980 ◽  
Vol 29 (3) ◽  
pp. 940-944 ◽  
Author(s):  
A E Metzler ◽  
R J Higgins ◽  
S Krakowka ◽  
A Koestner
Keyword(s):  
Tissue Culture ◽  
Neurological Disease ◽  
Canine Distemper Virus ◽  
In Vitro Growth ◽  
Canine Distemper ◽  
Passage Level ◽  
Pulmonary Macrophage

Virulence of canine distemper virus (CDV) adapted to in vitro growth in Vero or bovine cells was determined by inoculation into CDV-susceptible neonatal gnotobiotic dogs. When compared with dogs given virulent R252-CDV, Vero R252-CDV was attenuated at passage level 14. In contrast, dogs inoculated with bovine R252-CDV at the same passage level experienced rapid fatal neurological disease. Virulence was not linked to ability to infect or replicate in canine pulmonary macrophage cultures. Retention of virulence by bovine R252-CDV is unique and worthy of further study.

Viroid Elimination by Thermotherapy, Cold Therapy, Tissue Culture, In Vitro Micrografting, or Cryotherapy

2017 ◽  
pp. 425-435 ◽  
Author(s):  
Marina Barba ◽  
Munetaka Hosakawa ◽  
Qiao-Chun Wang ◽  
Anna Taglienti ◽  
Zhibo Zhang
Keyword(s):  
Tissue Culture ◽  
Culture In Vitro ◽  
Cold Therapy ◽  
In Vitro Micrografting

Development of Hydrogel Bioinks and 3D Bioprinting Techniques to Support Extended 3D Lung Tissue Culture In Vitro

2019 ◽  
Author(s):  
K.E. Bailey ◽  
N.J. Darling ◽  
D. Velu ◽  
T.J. D'Ovidio ◽  
M.L. Floren ◽  
...  
Keyword(s):  
Tissue Culture ◽  
Lung Tissue ◽  
3D Bioprinting ◽  
Culture In Vitro

MULTIPLICATION OF TULIP BULB BY TISSUE CULTURE IN VITRO

1986 ◽  
pp. 279-284 ◽  
Author(s):  
Y. Nishiuchi
Keyword(s):  
Tissue Culture ◽  
Tulip Bulb ◽  
Culture In Vitro

β-Criptoxanthin stimulates bone formation and inhibits bone resorption in tissue culture in vitro

2004 ◽  
Vol 258 (1/2) ◽  
pp. 137-144 ◽  
Author(s):  
Masayoshi Yamaguchi ◽  
Satoshi Uchiyama
Keyword(s):  
Tissue Culture ◽  
Bone Resorption ◽  
Bone Formation ◽  
Culture In Vitro

A Simplified Method for Quantitative Tissue Culture in vitro.

1930 ◽  
Vol 28 (3) ◽  
pp. 282-284 ◽  
Author(s):  
M. Sano ◽  
L. W. Smith
Keyword(s):  
Tissue Culture ◽  
Culture In Vitro ◽  
Simplified Method

scholarly journals Effect of synthetic auxins on in vitro and ex vitro bromeliad rooting

2013 ◽  
Vol 43 (2) ◽  
pp. 138-146 ◽  
Author(s):  
João Paulo Rodrigues Martins ◽  
Edilson Romais Schimildt ◽  
Rodrigo Sobreira Alexandre ◽  
Breno Régis Santos ◽  
Gizele Cristina Magevski
Keyword(s):  
Tissue Culture ◽  
Acetic Acid ◽  
Naphthalene Acetic Acid ◽  
Root Induction ◽  
In Vitro Growth ◽  
Free Medium ◽  
Ex Vitro ◽  
Synthetic Auxins ◽  
Parameters Analysis

The tissue culture can contribute to the propagation of several economic species, such as the bromeliads. This research aimed at evaluating the auxins type and concentration in the in vitro and ex vitro rhizogenesis of Neoregelia concentrica bromeliad. N. concentrica shoots were induced in a growth medium with 15.0 µM of 6-benzylaminopurine, for 80 days, followed by sub-cultivation in phytoregulator-free medium, for 45 days. In the in vitro rhizogenesis, the shoots grew in a medium supplemented with indole-3-butyric acid (IBA) or naphthalene-acetic acid (NAA), at the concentrations of 0.0 µM, 1.0 µM, 2.0 µM, 3.0 µM and 4.0 µM. In the ex vitro rhizogenesis, the bases of shoots were immersed, for 60 minutes, in IBA or NAA solutions, at the concentrations of 0.0 µM, 5.0 µM, 10.0 µM and 15.0 µM. After immersion, the shoots were planted in plastic trays with vermiculite. At the end of each rhizogenesis method, the phytotechnical parameters analysis was carried out. For the in vitro rhizogenesis, a higher number of roots were observed when the shoots were cultivated in concentrations higher than 1.0 µM of NAA, when compared to the IBA. However, the rooting rate differed only at 30 days after the in vitro growth, with a higher root induction in the shoots grown with NAA. At 60 days, the rooting rate was higher than 90% and statistically similar in all treatments. In the ex vitro rhizogenesis, a better formation of the rooting system was observed when 5.0 µM of IBA was applied, with higher rooting averages and number of roots.

Technique of Tissue Culture "In Vitro."

JAMA ◽  
1925 ◽  
Vol 84 (25) ◽  
pp. 1943
Keyword(s):  
Tissue Culture ◽  
Culture In Vitro
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