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1 ability to complement the dU2AF50 recessive lethal allele.
2 s mutation in a known carrier of a recessive lethal allele.
3 d random mutagenesis to create conditionally lethal alleles.
4 well as a limited subset of tub1 conditional-lethal alleles.
6 e encoding a dominant acting poison product, lethal alleles, and viable but UV-sensitive alleles isol
7 for EDNRB function, four recessive juvenile lethal alleles created by either radiation or chemical m
9 eneration of the intercrosses showed that no lethal alleles have accumulated on any of the neo-Y chro
11 In an attempt to identify unknown recessive lethal alleles in the current dairy population, a search
17 n for suppressors of a temperature-sensitive lethal allele of the C. elegans Aurora B kinase AIR-2.
31 for genetic interactions with two recessive lethal alleles of zipper in a second-site noncomplementa
32 yprinidae), the average numbers of recessive lethal alleles per individual are 1.9 (95% confidence li
33 many individuals carry one or more recessive lethal alleles, posing an evolutionary conundrum for the
35 sses between F0 animals that carry embryonic lethal alleles recapitulate loss-of-function phenotypes,
36 the accumulation of strongly deleterious or lethal alleles, swamping the effect of any potentially a
37 es are distinct from those of two classes of lethal alleles (termed I and II) that show intergroup, i
39 a1) suppresses several temperature-sensitive lethal alleles that affect chromosome replication and ch
40 n defined by temperature-sensitive embryonic lethal alleles that strongly affect germline meiosis and
41 enomes) to generate three weaker, non-embryo-lethal, alleles (tps1-11, tps1-12 and tps1-13) and use t
42 s within the CRO1/She4p-like domain, and two lethal alleles were found to result from stop codon muta
44 tant plants from strong maternal gametophyte lethal alleles, which is not possible via conventional d
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