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Abstract Exposure levels without appreciable human health risk may be determined by dividing a point of departure on a dose–response curve (e.g., benchmark dose) by a composite adjustment factor (AF). An “effect severity” AF (ESAF) is employed in some regulatory contexts.
Barbara L. Parsons +17 more
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Dataset of 16S ribosomal DNA sequence-based identification of bacteriocinogenic lactic acid bacteria isolated from fermented food samples. [PDF]
Imade EE +5 more
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Circular ribosomal DNA and ribosomal DNA: replication in somatic amphibian cells
Chromosoma, 1975Pulse labelled rDNA from cultured somatic cells of Xenopus laevis was examined by electron microscope autoradiography. The pattern of replication closely resembles that of bulk chromosomal DNA and differs considerably from rDNA synthesis during amplification in the oocyte.
J D, Rochaix, A P, Bird
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Heterogeneity in cucumber ribosomal DNA
Theoretical and Applied Genetics, 1986Restriction and hybridization analysis of cucumber native ribosomal (r) DNA purified from actinomycin-D/CsCl gradients suggested that the repeat units were heterogeneous in both length and sequence. Several full length rDNA repeat units were cloned and five are described which account for all the EcoR I and Xba I fragments present in native DNA. One of
T A, Kavanagh, J N, Timmis
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Ribosomal DNA of Caenorhabditis elegans
Journal of Molecular Biology, 1981Abstract We have characterized the organization of the genes coding for 18 S, 5·8 S and 26 S ribosomal RNAs in the nematode Caenorhabditis elegans . These ribosomal genes, present in about 55 copies per haploid genome, alternate in a repeating tandem array.
J G, Files, D, Hirsh
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Nature, 1969
THE amount of DNA complementary to ribosomal RNA (rDNA) has been shown to be constant in several tissues varying in rRNA synthesis1,2. There is, however, a dramatic exception to this in amphibian and insect oocytes3–5, where amplification of the rDNA occurs and results in high rates of rRNA synthesis during oogenesis6.
J, Mohan, A, Dunn, L, Casola
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THE amount of DNA complementary to ribosomal RNA (rDNA) has been shown to be constant in several tissues varying in rRNA synthesis1,2. There is, however, a dramatic exception to this in amphibian and insect oocytes3–5, where amplification of the rDNA occurs and results in high rates of rRNA synthesis during oogenesis6.
J, Mohan, A, Dunn, L, Casola
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Non-canonical DNA structures in the human ribosomal DNA
Histochemistry and Cell Biology, 2023Non-canonical structures (NCS) refer to the various forms of DNA that differ from the B-conformation described by Watson and Crick. It has been found that these structures are usual components of the genome, actively participating in its essential functions.
Evgeny, Smirnov +4 more
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Circular ribosomal DNA during ribosomal magnification in Drosophila melanogaster
Journal of Molecular Biology, 1977DNA from excised testes of Drosophila melanogaster males undergoing ribosomal DNA magnification shows two peaks on an ethidium bromide/CsCl density gradient: a minor peak that bands to a density of 1·570 g/cm3 and a main peak corresponding to 1·540 g/cm3 density.
F. GRAZIANI +2 more
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Structure and organization of ribosomal DNA
Biochimie, 1991Three trends are seen in the organization of ribosomal DNA genes during evolution: 1) gradual separation and separability of the regulation of transcription of 5S and larger subunit rRNAs; 2) retention of a transcription unit containing both large and small rRNAs; and 3) clustering of genes for both 5S and 18S-28S rDNAs, with the possible association ...
A K, Srivastava, D, Schlessinger
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