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2 rosatellite scan together with outcrosses to Mus spretus and M. castaneous followed by a subsequent t
4 k contrast, CDK3 from two wild-mice species (Mus spretus and Mus mus castaneus) lack this mutation.
5 tribution of IAPE elements in the genomes of Mus spretus and Mus musculus inbred strains and wild-cau
6 ngth variation between Mus musculus spp. and Mus spretus, and 32% showed variation between Mus muscul
7 wild mouse species, including Mus musculus, Mus spretus, and Mus spicelegus, as well as some inbred
8 o a second locus on proximal Chromosome 6 in Mus spretus, and this partial duplication was confirmed
9 length and ageing in mice, we have utilized Mus spretus as a model species because it has telomere l
10 other loci in three separate Mus musculus x Mus spretus backcross panels, we established the order o
12 channel 4) to band F4 of the X chromosome in Mus spretus but to chromosome 7 in laboratory strains.
13 is X-linked and subject to X inactivation in Mus spretus, but that the same gene is autosomal in labo
15 e performed RNA sequencing in Mus musculus x Mus spretus cells with complete skewing of X inactivatio
16 To determine if the polytropic proviruses of Mus spretus contain functional genes, we inoculated neon
20 c backcross panel from the cross (C57BL/6J x Mus spretus)F1 x Mus spretus probed with the mouse COX V
21 p16) and Cdkn2b(p15), and between BALB/c and Mus spretus for Cdkn2c(p18(INK4c)) were used to position
22 terspecific crosses between Mus musculus and Mus spretus for the detection of strong genetic interact
23 imprinting is investigated by introducing a Mus spretus H19 gene into heterologous locations in the
26 susceptibility in interspecific Mus musculus/Mus spretus hybrid mice and have identified another seve
27 interspecific mouse crosses (Mus musculus x Mus spretus) identified the gene encoding Aurora2 (Stk6
29 everal wild mice (Mus dunni, SC-1 cells, and Mus spretus) mediated infections by both X-MLVs and P-ML
34 ed to cytoplasts prepared from Mus musculus, Mus spretus, or rat (Rattus norvegicus), a comparable nu
37 rom 45 different strains of Mus musculus and Mus spretus revealed extensive polymorphism involving al
40 ween C57BL/6J (B6) and either C3H/HeJ (H) or Mus spretus (SPRET) occurred in four zones (A-D); zone A
41 omal clones) to map sequence variation among Mus spretus (SPRET/Ei and SPRET/Glasgow) and Mus musculu
42 Mus musculus (telomere length >25 kb) and Mus spretus (telomere length 5-15 kb) were used to gener
43 SPRET/Ei is an inbred strain derived from Mus spretus that has approximately 1% sequence differenc
46 musculus domesticus) and the Algerian mouse (Mus spretus), using samples from the ranges of sympatry
47 olymorphism in intron 2 between C57BL/6J and Mus spretus was used to map this gene to Chromosome 5 ne
48 hat are polymorphic between Mus musculus and Mus spretus, we used The Jackson Laboratory (TJL) inters
50 of three independent Mus musculus NIH/Ola x (Mus spretus x M. musculus NIH/Ola)F1 backcrosses, to ide
52 ed by the backcross of (lean C57BL/6J x lean Mus spretus) x C57BL/6J, provides an excellent model of
53 [F1 female Spd/+ (female Spd/+ B6 x male +/+ Mus spretus) x male +/+ B6] exhibit highly variable cran
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