Results 201 to 210 of about 33,908 (236)
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RAPD in the analysis of isolates of Entamoeba histolytica
Acta Tropica, 2000Genetic variability in Entamoeba histolytica was analyzed by random amplified polymorphic DNA (RAPD) using ten arbitrary primers. Due to intrinsic characteristics of the RAPD technique only axenic samples were analyzed. since the presence of any microorganism in the cultures interfered in the DNA profile by generating RAPDs not pertaining to E ...
M A, Gomes +4 more
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Inheritance of RAPDs in F1 hybrids of corn
Theoretical and Applied Genetics, 1993Random amplified polymorphic DNA (RAPD) markers were analyzed in materials from a partial diallel, including 16 corn F1 hybrids (with five reciprocals) and their five parental inbreds. Using 21 primers, we scored a total of 140 different fragments for their presence/absence and intensity variation, where appropriate.
M, Heun, T, Helentjaris
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Competition as a source of errors in RAPD analysis
TAG Theoretical and Applied Genetics, 1996We have used artificial 1∶1 DNA mixtures of all pairwise combinations of four doubled haploid Brassica napus lines to test the ability of RAPDs to function as reliable dominant genetic markers. In situations where a specific RAPD band is present in one homozygous line but absent in the other, the band is expected in the artificial heterozygote, i.e. in
C, Halldén +4 more
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2002
Randomly amplified polymorphic DNA (RAPD)- polymerase chain reaction (PCR) is a simple and inexpensive tool enabling the study of genetic variation at population level. It can also be applied at the species or subgeneric level to examine phylogenetic questions (e.g., Yoon and Bae 1995, Altomare et al 1997, Gandeboeuf et al. 1997).
H. Thorsten Lumbsch, Imke Schmitt
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Randomly amplified polymorphic DNA (RAPD)- polymerase chain reaction (PCR) is a simple and inexpensive tool enabling the study of genetic variation at population level. It can also be applied at the species or subgeneric level to examine phylogenetic questions (e.g., Yoon and Bae 1995, Altomare et al 1997, Gandeboeuf et al. 1997).
H. Thorsten Lumbsch, Imke Schmitt
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2014
?????????????????????? ?????????????? ?????????????????????? ?????????????? ???? ?????????? ?????? (Glycine max L., Merr.) ?? ???????????????????? ?? ?????????????????? (WR) ?????????????????? ??????????. WR-?????????? ???????????????????? ???????????????????????? ???????????????????????? ?? ?????????????????????? V??????. ?????????????????????? ???????
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?????????????????????? ?????????????? ?????????????????????? ?????????????? ???? ?????????? ?????? (Glycine max L., Merr.) ?? ???????????????????? ?? ?????????????????? (WR) ?????????????????? ??????????. WR-?????????? ???????????????????? ???????????????????????? ???????????????????????? ?? ?????????????????????? V??????. ?????????????????????? ???????
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2021
By random amplified polymorphic DNA we studied trasgeneration consequences of radiation treatment. We estimated RAPD-patterns in offspring of experimental and control groups according to the rates of new ???not parental bands??? and the average frequency of appearance new bands per mouse. We revealed increase of rate and frequency not parental bands in
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By random amplified polymorphic DNA we studied trasgeneration consequences of radiation treatment. We estimated RAPD-patterns in offspring of experimental and control groups according to the rates of new ???not parental bands??? and the average frequency of appearance new bands per mouse. We revealed increase of rate and frequency not parental bands in
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2017
Genetic variability of amaranth collection was studied with RAPD-analysis. A high level of polymorphism of studied accessions was determined and amounted 85 % in mean. The unique bends characteristic only for the definite accessions, and 18 monomorphic loci proper for all amaranth accessions were detected with some primers. The genetic distances of Nei
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Genetic variability of amaranth collection was studied with RAPD-analysis. A high level of polymorphism of studied accessions was determined and amounted 85 % in mean. The unique bends characteristic only for the definite accessions, and 18 monomorphic loci proper for all amaranth accessions were detected with some primers. The genetic distances of Nei
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2010
???????????????? RAPD-PCR ???????????? ?????????????? ???????????????? ?????????? ?????????????????? ?????? (46 ????????????). ???????? ???????????? ?????????????????????????? ?????????????????? ?????????????????????? ?????????????????? ?????????????????? ???????????? Acipenser schrenckii Brandt, 1869 ?? ???????????? Huso dauricus (Georgi, 1775). ??????
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???????????????? RAPD-PCR ???????????? ?????????????? ???????????????? ?????????? ?????????????????? ?????? (46 ????????????). ???????? ???????????? ?????????????????????????? ?????????????????? ?????????????????????? ?????????????????? ?????????????????? ???????????? Acipenser schrenckii Brandt, 1869 ?? ???????????? Huso dauricus (Georgi, 1775). ??????
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Optimization of RAPD Fingerprinting
1997RAPD fingerprinting has been extensively used to detect DNA sequence polymorphism in many plant, bacterial and fungal species (Williams et al. 1990; Kresovich et al. 1992; Cobb and Clarkson 1993). In addition, tightly linked RAPD markers have been used to detect breeding lines containing specific gene blocks facilitating marker-based selection and ...
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?????????????? ???????????????????????????? ?????? ???? ???????????????????? RAPD-PCR
2015The results of reamplification of flax DNA with random primers are represented. It was shown that eight of 17 decameric primers used in the experiments had an reamplification effect: the intensity of the bands increased; new bands and/or new polymorphic bands appeared in the gel sample.
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