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Previous efforts to map variation in other species include strain specific mouse resequencing [ 3, 4], a haplotype mapping in rat [ 5], as well as data mining of public domain resources such as NCBI's dbSNP [ 6].
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Thus, there was no clear correlation between R-band and GC3 of the mapped genes in rat snake.
By using β-radio imager whole-body mapping in rats, we have shown that systematically administered HB-19 is rapidly cleared from blood to become distributed selectively in tissues expressing enhanced levels of surface nucleolin, where a significant proportion still persists even after 24 hours in its active form [39].
We have also successfully demonstrated the capability of the system for sentinel lymph node mapping in rats.
We conducted a non-invasive preclinical study of fluorescent sentinel lymph node mapping in rats (n = 5) with our fiber-based, video-rate fluorescence DOT system.
They prefer simple visual cues, so there seems no reason to assume multimodal cognitive mapping in rats; their behavior would be fully explainable in terms of tracking environmental cues, just like tropisms or taxis are used in simpler organisms.
We discovered that the emergence of a direction map in rat barrel cortex occurs long after all known critical periods in the somatosensory system.
Similar numbers of loci have been mapped in rat models of arthritis: 29 for CIA, 39 for PIA, eight for oil-induced arthritis and five controlling adjuvant-induced arthritis [ 67].
In the absence of reliable antibodies for the GLP-1 receptor, the targets for GLP-1 in the brain have been mapped in rat either by identifying GLP-1 binding sites [ 26] or by in situ hybridisation for GLP-1 receptor mRNA [ 17].
The use of genetic markers for mapping traits in rat strains has been exploited for long time already.
Traditionally, QTL mapping studies in rat (Rattus norvegicus) have been limited by the availability of markers and often focused marker development was needed to successfully link genomic regions to a specific trait (for example [ 5, 6]).
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