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1    The corn1 locus was mapped using selected back-crosses.
2                          Interspecific mouse back-cross analysis identified the loci for mouse 3Ost g
3 l rapid mapping strategy incorporating speed back-crosses and high throughput genotyping.
4                                              Back-cross animals were generated using in vitro fertili
5                     Therefore, we used an N2 back-cross between the inbred C57BL/6 and FVB/N strains
6                       In this study, we used back-crossed FVB wild-type (WT) and AIB1 mutant mice to
7 mice were generated in the 129S6 strain, and back-crossed into the C57BL/6J genetic background.
8 ies per plant) were maintained by continuous back-crossing into a phenotypically uniform inbred backg
9 ale and female progeny from an intraspecific back-cross involving BN: supports a gene order of cen-DX
10 nsgene-negative H2b/q F1 or first-generation back-crossed mice rejected H2b marrow grafts (hybrid res
11 neration in the hippocampus by assessing 331 back-cross (N2) progeny of two inbred mouse strains, C57
12 pulation can be generated either from double back-cross of immortalized F2 (IF2) to the two parents,
13 use the offspring (IL-10-NOD-scid mice) from back-crosses of IL-10-NOD mice with NOD-scid mice had no
14 d first exon were deleted ubiquitously, were back-crossed onto a BALB/c background, and studied with
15 king platelet supervillin were generated and back-crossed onto a C57BL/6 background.
16 ry tumor formation, the p53(null) allele was back-crossed onto the BALB/c genetic background.
17 genesis of the XLH, Mepe-deficient mice were back-crossed onto the Hyp mouse homologue of XLH and phe
18 egated as complex genetic traits in F(1) and back-cross progeny.
19                               Examination of back-crossed progeny confirmed that all the insertions e
20               B6Tg2576 mice were produced by back-crossing Tg2576 mice, an AD mouse model overexpress
21 an affect susceptibility to cranial NTDs, by back- crossing the splotch ( Sp (2H) ) mutant gene onto
22  role of 24p3, we derived 24p3 null mice and back-crossed them onto C57BL/6 and 129/SVE backgrounds.
23  Nu/nu F1 hybrid females were identified and back-crossed to homozygous male nude mice to produce AR-
24 es in disease progression, CD46(+) mice were back-crossed to T- and B-cell-deficient RAG-2 knockout m
25 lpha regulatory subunit of the PI3K and were back-crossed to ultimately generate offspring with cone-
26 ckground have normal eyelid development, but back-crossing to BALB/c background for four or five gene
27 ces in phenotype ratios among the reciprocal back-crosses were consistent with parental imprinting.
28         FVB.Ly49IB6+/- mice were crossed and back-crossed with 129 mice-H2b, 5E6-, poor responders to
29 e and the mutagenized endonuclease gene; (3) back-crosses with the wild-type gene by ligation to the
30              The transgene was eliminated by back-crossing with wild-type Arabidopsis.

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