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Intriguingly, the 2.1 Å density map of bovine CIII clearly shows that it contains two opposite orientations of the full-length UQCRFS1N peptide (1 78 amino acids), with the N terminal binding in one CIII protomer and the C terminal binding in the other CIII protomer (Fig. 1C E).
In the previous study, we reported the first descriptive map of bovine GV oocytes and their potentially-interacting cumulus cells with specific emphasis on membrane, nuclear proteins, receptor-ligand pairs, and transcription factors.
Here, we report the map of bovine CNVs.
In this study, we describe a map of bovine CNVs and provide important resources for future bovine genome research.
A 12 k Radiation hybrid map of bovine chromosome 14 was constructed using 843 single nucleotide polymorphism markers.
We have built a high resolution RH map of bovine chromosomes 19 and 29 consisting of 555 and 253 SNP markers, respectively.
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Cryo-electron microscopy and icosahedral image analysis was used to define the structural basis for this difference in transcriptase activity and to derive three-dimensional density maps of bovine UK and human Wa DLPs at 26 Å and 28 Å resolution, respectively.
Linkage maps of bovine autosomes with these SNPs represent 4585 markers in 2475 positions spanning 3058 cM.
The objective of the present study was to generate high resolution RH maps of bovine chromosomes 19 (BTand) and 29 (BTand), and compare them with the current 7.1X bovine genome sequence assembly (bovine build 3.1).
Such a temporal expression pattern, where peak production of IL-10 lags behind that of IFN-γ, has also been demonstrated in relation to MAP stimulation of bovine PBMC [ 50].
Here we report a second generation RH map of the bovine genome which can be used to improve the construction of an integrated bovine genomic map.
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