Results 21 to 30 of about 170,575 (305)

The highly rearranged mitochondrial genomes of the crabs Maja crispata and Maja squinado (Majidae) and gene order evolution in Brachyura [PDF]

open access: yes, 2017
We sequenced the mitochondrial genomes of the spider crabs Maja crispata and Maja squinado (Majidae, Brachyura). Both genomes contain the whole set of 37 genes characteristic of Bilaterian genomes, encoded on both \u3b1- and \u3b2-strands.
AD Miller   +67 more
core   +1 more source

Cooperativity dominates the genomic organization of p53-response elements: a mechanistic view.

open access: yesPLoS Computational Biology, 2009
p53-response elements (p53-REs) are organized as two repeats of a palindromic DNA segment spaced by 0 to 20 base pairs (bp). Several experiments indicate that in the vast majority of the human p53-REs there are no spacers between the two repeats; those ...
Yongping Pan, Ruth Nussinov
doaj   +1 more source

Structural basis of copper-efflux-regulator-dependent transcription activation

open access: yesiScience, 2021
Summary: The copper efflux regulator (CueR), a representative member of mercury resistance regulator (MerR) family metalloregulators, controls expression of copper homeostasis-regulating genes in bacteria.
Wei Shi   +8 more
doaj   +1 more source

Functional analysis of transcribed spacers of yeast ribosomal DNA. [PDF]

open access: yesThe EMBO Journal, 1990
Making use of an rDNA unit, containing oligonucleotide tags in both the 17S and 26S rRNA gene, we have analyzed the effect of various deletions in the External Transcribed Spacer (ETS) and in one of the Internal Transcribed Spacers 1 (ITS1) on the process of ribosome formation in yeast.
W, Musters   +4 more
openaire   +2 more sources

Improved split fluorescent proteins for endogenous protein labeling. [PDF]

open access: yes, 2017
Self-complementing split fluorescent proteins (FPs) have been widely used for protein labeling, visualization of subcellular protein localization, and detection of cell-cell contact.
Feng, Siyu   +5 more
core   +2 more sources

An ancestral genomic sequence that serves as a nucleation site for de novo gene birth.

open access: yesPLoS ONE, 2022
The process of gene birth is of major interest with current excitement concerning de novo gene formation. We report a new and different mechanism of de novo gene birth based on the finding and the characteristics of a short non-coding sequence situated ...
Nicholas Delihas
doaj   +2 more sources

CRISPR interference directs strand specific spacer acquisition.

open access: yesPLoS ONE, 2012
BackgroundCRISPR/Cas is a widespread adaptive immune system in prokaryotes. This system integrates short stretches of DNA derived from invading nucleic acids into genomic CRISPR loci, which function as memory of previously encountered invaders.
Daan C Swarts   +3 more
doaj   +1 more source

RAG-1 Mutations Associated with B-Cell-Negative SCID Dissociate the Nicking and Transesterification Steps of V(D)J Recombination [PDF]

open access: yes, 2001
Some patients with B-cell-negative severe combined immune deficiency (SCID) carry mutations in RAG-1 or RAG-2 that impair V(D)J recombination. Two recessive RAG-1 mutations responsible for B-cell-negative SCID, R621H and E719K, impair V(D)J recombination
Chang, Fu-Chung   +2 more
core   +2 more sources

Evaluation of five regions as DNA barcodes for identification of Lepista species (Tricholomataceae, Basidiomycota) from China [PDF]

open access: yesPeerJ, 2019
Background Distinguishing among species in the genus Lepista is difficult because of their similar morphologies. Methods To identify a suitable DNA barcode for identification of Lepista species, we assessed the following five regions: internal ...
Siyu Wang   +5 more
doaj   +2 more sources

The structure of the maize ribosomal DNA spacer region

open access: yesNucleic Acids Research, 1986
A combination of a single stranded plasmid vector and ordered deletions were used to determine the complete nucleotide sequence of a rDNA spacer region isolated from the DNA of maize Black Mexican Sweet suspension cells. The sequence reveals the presence of ten "200 base" subrepeats within the maize rDNA spacer region.
M D, McMullen   +3 more
openaire   +3 more sources

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