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1 The corn1 locus was mapped using selected back-crosses.
2 d after successful interbreeding followed by back-crossing.
7 fortis and G. scandens, hybridize rarely and back-cross bidirectionally with little or no loss of fit
10 ies per plant) were maintained by continuous back-crossing into a phenotypically uniform inbred backg
11 ale and female progeny from an intraspecific back-cross involving BN: supports a gene order of cen-DX
12 nsgene-negative H2b/q F1 or first-generation back-crossed mice rejected H2b marrow grafts (hybrid res
13 neration in the hippocampus by assessing 331 back-cross (N2) progeny of two inbred mouse strains, C57
14 pulation can be generated either from double back-cross of immortalized F2 (IF2) to the two parents,
15 use the offspring (IL-10-NOD-scid mice) from back-crosses of IL-10-NOD mice with NOD-scid mice had no
16 d first exon were deleted ubiquitously, were back-crossed onto a BALB/c background, and studied with
19 genesis of the XLH, Mepe-deficient mice were back-crossed onto the Hyp mouse homologue of XLH and phe
23 an affect susceptibility to cranial NTDs, by back- crossing the splotch ( Sp (2H) ) mutant gene onto
24 role of 24p3, we derived 24p3 null mice and back-crossed them onto C57BL/6 and 129/SVE backgrounds.
26 Nu/nu F1 hybrid females were identified and back-crossed to homozygous male nude mice to produce AR-
27 es in disease progression, CD46(+) mice were back-crossed to T- and B-cell-deficient RAG-2 knockout m
28 lpha regulatory subunit of the PI3K and were back-crossed to ultimately generate offspring with cone-
29 ckground have normal eyelid development, but back-crossing to BALB/c background for four or five gene
30 uld be used with caution or with appropriate back-crossing to other C57BL/6J mouse substrain lines wi
31 ces in phenotype ratios among the reciprocal back-crosses were consistent with parental imprinting.
33 e and the mutagenized endonuclease gene; (3) back-crosses with the wild-type gene by ligation to the