Spontaneous production of a C-type rna virus in rat tissue culture lines

1973 ◽  
Vol 12 (3) ◽  
pp. 654-666 ◽  
Author(s):  
V. Klement ◽  
M. O. Nicolson ◽  
W. Nelson-Rees ◽  
R. V. Gilden ◽  
S. Oroszlan ◽  
...  
Keyword(s):  
Tissue Culture ◽  
Rna Virus ◽  
Spontaneous Production ◽  
Rat Tissue

Highly efficient heritable genome editing in wheat using an RNA virus and bypassing tissue culture

2021 ◽  
Author(s):  
Tingdong Li ◽  
Jiacheng Hu ◽  
Yu Sun ◽  
Boshu Li ◽  
Dingliang Zhang ◽  
...  
Keyword(s):  
Tissue Culture ◽  
Genome Editing ◽  
Rna Virus ◽  
Highly Efficient

Cytotoxic Effect of Nephrotoxic Serum on Rat Tissue Culture.

1957 ◽  
Vol 95 (2) ◽  
pp. 331-335 ◽  
Author(s):  
C. T. Liu ◽  
W. W. McCrory ◽  
J. A. Flick
Keyword(s):  
Tissue Culture ◽  
Cytotoxic Effect ◽  
Rat Tissue

Induction of an endogenous B-tropic type C RNA virus from SWR/J mouse embryo cells in tissue culture

Virology ◽  
1976 ◽  
Vol 70 (2) ◽  
pp. 352-359 ◽  
Author(s):  
John R. Stephenson ◽  
Stuart A. Aaronson
Keyword(s):  
Tissue Culture ◽  
Mouse Embryo ◽  
Rna Virus ◽  
Embryo Cells ◽  
Type C

Toxicity of Bilirubin and Bilirubin Diglucuronide to Rat Tissue Culture Fibroblasts

1988 ◽  
Vol 20 (3) ◽  
pp. 190-194 ◽  
Author(s):  
M. Taube ◽  
P. Elliot ◽  
H. Ellis
Keyword(s):  
Tissue Culture ◽  
Rat Tissue

Glass-ionomer cement implant/bone interface in primate and rat tissue culture models

Bone ◽  
1992 ◽  
Vol 13 (1) ◽  
pp. 98-98 ◽  
Author(s):  
P.V. Hatton ◽  
I.M. Brook ◽  
L.M. Jonck
Keyword(s):  
Tissue Culture ◽  
Glass Ionomer Cement ◽  
Glass Ionomer ◽  
Bone Interface ◽  
Culture Models ◽  
Rat Tissue ◽  
Ionomer Cement

scholarly journals The Presence of C-type RNA Virus Particles in a Rat Embryo Cell Line Spontaneously Transformed in Tissue Culture

1971 ◽  
Vol 12 (3) ◽  
pp. 303-311 ◽  
Author(s):  
L. Gazzolo ◽  
D. Simkovic ◽  
M. C. Martin-Berthelon
Keyword(s):  
Tissue Culture ◽  
Cell Line ◽  
Rna Virus ◽  
Embryo Cell ◽  
Rat Embryo ◽  
Virus Particles

Production of clonal plantlets of tropical pine in tissue culture via axillary shoot activation

1989 ◽  
Vol 19 (10) ◽  
pp. 1338-1342 ◽  
Author(s):  
R. Baxter ◽  
S. N. Brown ◽  
N. F. England ◽  
C. H. M. Ludlow ◽  
S. L. Taylor ◽  
...  
Keyword(s):  
Tissue Culture ◽  
Activated Charcoal ◽  
Shoot Elongation ◽  
Axillary Bud ◽  
Axillary Shoot ◽  
Axillary Shoots ◽  
Spontaneous Production ◽  
Bud Initiation

A method for the production of multiple clonal plantlets of Pinuscaribaea var. hondurensis Morlet, P. oocarpa Schiede, and P. tecunumanii Equiluz and Perry (P. patula Schiede and Deppe ssp. tecunumanii (Equiluz and Perry) Styles) from juvenile sources is described. The procedure is based on the spontaneous production of axillary shoots following shoot elongation. Much interclonal variation exists with respect to expiant multiplication. The addition of activated charcoal (0.1%) stimulates shoot elongation, especially in recalcitrant clones of P. caribaea. Axillary bud initiation may be stimulated by 6-benzylaminopurine, but levels above 1 μM can result in failure of induced buds to form shoots. Rooting occurs at about 50% in nonsterile peat–perlite medium without auxin pretreatment. Rooted plantlets can be readily hardened and will grow normally in the glasshouse.

Spontaneous Production of a C-Type RNA Virus in a Cell Line Derived from Rat Glioma

1979 ◽  
Vol 23 (1) ◽  
pp. 1-15 ◽  
Author(s):  
Koichi Igarashi ◽  
Reiko Sasada ◽  
Yasuhiko Niiyama ◽  
Yoshio Kozai ◽  
Yukio Sugino
Keyword(s):  
Cell Line ◽  
Rna Virus ◽  
Rat Glioma ◽  
Spontaneous Production ◽  
A Cell

Tissue section lifting for electron microscopy

1978 ◽  
Vol 36 (2) ◽  
pp. 86-87
Author(s):  
Adrian F. van Dellen
Keyword(s):  
Infectious Disease ◽  
Electron Microscopy ◽  
Tissue Culture ◽  
Organ System ◽  
Surrounding Tissue ◽  
Paraffin Sections ◽  
Surface Areas ◽  
Specific Determination ◽  
High Degree ◽  
Accuracy And Repeatability

The morphologic pathologist may require information on the ultrastructure of a non-specific lesion seen under the light microscope before he can make a specific determination. Such lesions, when caused by infectious disease agents, may be sparsely distributed in any organ system. Tissue culture systems, too, may only have widely dispersed foci suitable for ultrastructural study. In these situations, when only a few, small foci in large tissue areas are useful for electron microscopy, it is advantageous to employ a methodology which rapidly selects a single tissue focus that is expected to yield beneficial ultrastructural data from amongst the surrounding tissue. This is in essence what "LIFTING" accomplishes. We have developed LIFTING to a high degree of accuracy and repeatability utilizing the Microlift (Fig 1), and have successfully applied it to tissue culture monolayers, histologic paraffin sections, and tissue blocks with large surface areas that had been initially fixed for either light or electron microscopy.

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