Results 251 to 260 of about 93,372 (292)
Some of the next articles are maybe not open access.

Ribosomal RNA and rDNA sequence analyses

Gene, 1992
The potential of ribosomal (r) RNA and the encoding genes (rDNA) to elucidate natural relationships has been dramatically extended by improved sequencing approaches and the application of polymerase chain reaction. Sequence information on 16S and 23S rRNA/DNA from 69 strains of 53 Streptomyces species allows determination of regions that can be used as
Stackebrandt, Erko   +2 more
openaire   +4 more sources

Amplification of rDNA and type I sequences in Drosophila males deficient in rDNA

Cell, 1983
rDNA magnification is a heritable change in rDNA content that occurs in D. melanogaster males when chromosomes deficient in rDNA are placed together for several generations. We have examined the restriction endonuclease cleavage pattern of the rDNA from an X chromosome undergoing magnification, and find no evidence for the selective amplification of ...
D V, de Cicco, D M, Glover
openaire   +2 more sources

rDNA magnification in D. melanogaster: State of rDNA copies following the first step

Molecular and General Genetics MGG, 1979
D. melanogaster males of XYbb/O genetic constitution undergoing rDNA magnification were mated singly to XXbb+/O females, yielding XYbb/O male progeny, and to XNO- w sn bb+ females, yielding XYbb/XNO- females. The male and female offspring were scored for the bb+ phenotype.
Graziani F, LA MANTIA, GIROLAMA
openaire   +3 more sources

SSU rDNA phylogeny of cladoniiform lichens

American Journal of Botany, 1998
To examine phylogenetic relationships among the “cladoniiform” lichenized fungi, i.e., the families Cladoniaceae, Baeomycetaceae, Icmadophilaceae, Stereocaulaceae, and Siphulaceae, and to provide evidence for the anticipated independent origins of podetia and pseudopodetia, we conducted phylogenetic analyses of SSU (small subunit) rDNA sequences from ...
S K, Stenroos, P T, Depriest
openaire   +2 more sources

16S rDNA methods in soil microbiology

Current Opinion in Biotechnology, 1999
With the introduction of molecular methods, the past decade has seen renewed interest in soil microbiology. New and exciting molecular technologies and the promise of finally opening the microbial black box in soil drive much of this interest. Although these pioneering studies have added much to our knowledge of microbial diversity in soils, it is ...
, O'Donnell, , Gorres
openaire   +2 more sources

rDNA Transcription during Xenopus laevis Oogenesis

Biochemical and Biophysical Research Communications, 2002
It is generally believed that, during Xenopus laevis oogenesis, polymerase I transcription is high in the early vitellogenic oocytes (stages III and IV) and very low in later stages. We used a combination of RNA labeling, nuclease S1 protection assays, Northern blot, and half-life measurement of preribosomal RNA to reinvestigate the pattern of ...
Roger, B.   +3 more
openaire   +3 more sources

Regulation of rDNA stability by sumoylation

DNA Repair, 2009
Repair of DNA lesions by homologous recombination relies on the copying of genetic information from an intact homologous sequence. However, many eukaryotic genomes contain repetitive sequences such as the ribosomal gene locus (rDNA), which poses a risk for illegitimate recombination.
Eckert-Boulet, Nadine, Lisby, Michael
openaire   +3 more sources

rDNA Amplification: Application of 16S rDNA-Based Methods for Bacterial Identification

2000
Continuing improvements in PCR and automated sequencing technologies, resulting in rapid acquisition of sequence data, have allowed these methods to be applied to the task of bacterial identification. The sequence of the 16S rDNA/RNA of bacterial strains has been demonstrated to be useful for phylogenetic analysis of different taxa.
Frederick A. Rainey, Erko Stackebrandt
openaire   +1 more source

Citrus 16S rDNA microbiom

16S rDNA amplicon sequencing of citrus rhizosphere and endophyte microbiome.
openaire   +1 more source

การจำแนกสปีชีส์ของเชื้อมัยโคแบคทีเรียมโดยหาลำดับเบสของชิ้นส่วน 16S rDNA ที่เพิ่มจำนวน

ทำการศึกษาเพื่อแยกสปีชีส์ของเชื้อมัยโคแบคทีเรีย โดยการหาลำดับเบสของชิ้นส่วน 16S rDNA ที่เพิ่มจำนวนด้วยเทคนิค polymerase chain reaction เปรียบเทียบกับวิธีที่ใช้อยู่ประจำ (conventional method) โดยอาศัยลักษณะของโคโลนี การสร้างสี อัตราการเจริญเติบโตปฏิกิริยาชีวเคมี และ Accuprobe ในการศึกษาใช้เชื้อมัยโคแบคทีเรียมาตรฐาน 16 สปีชีส์ และเชื้อมัยโคแบคทีเรียท ...
openaire   +1 more source

Home - About - Disclaimer - Privacy