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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.
5 erated mutants, we identified an independent lethal allele and an RNAi off-target effect that prevent
6 ing depression in plants is primarily due to lethal alleles and possibly epistatic interactions.
7 e encoding a dominant acting poison product, lethal alleles, and viable but UV-sensitive alleles isol
8                                              Lethal alleles are mutations in the genome that cause em
9  for EDNRB function, four recessive juvenile lethal alleles created by either radiation or chemical m
10                            The conditionally lethal alleles exhibit a variety of phenotypes under res
11 eneration of the intercrosses showed that no lethal alleles have accumulated on any of the neo-Y chro
12 id individual, and high frequencies of haplo-lethal alleles in natural populations.
13  In an attempt to identify unknown recessive lethal alleles in the current dairy population, a search
14 aled unexpectedly low numbers of segregating lethal alleles in two species of fish.
15                     To examine the recessive-lethal alleles in vitro, we devised a novel method to re
16        We describe two temperature-sensitive lethal alleles (mus209(B1) and mus209(2735)) of the Dros
17                 Furthermore, we identified a lethal allele of MCM10 that stimulates initial DNA unwin
18 P1 in a suppressor screen with a conditional lethal allele of SPC29.
19 n for suppressors of a temperature-sensitive lethal allele of the C. elegans Aurora B kinase AIR-2.
20       We found that the protein encoded by a lethal allele of the DROSOPHILA: modifier of mdg4 [mod(m
21 tegy was applied to generate a conditionally lethal allele of yraM.
22 hila morphogenesis, we have isolated several lethal alleles of crossveinless-c (cv-c).
23 was isolated from a library of conditionally lethal alleles of DIM1.
24 nt maternal enhancers of recessive embryonic lethal alleles of dpp and screw.
25 as maternal enhancers of recessive embryonic lethal alleles of dpp.
26             We have isolated two late-larval lethal alleles of Drosophila Myb.
27                                    Embryonic lethal alleles of ed reveal a role of Ed in restricting
28                                              Lethal alleles of MCM6 reveal it is essential for mitoti
29                            In strong, larval lethal alleles of morula, the polytene ring gland cells
30                                              Lethal alleles of orc6 are defective in DNA replication
31                                              Lethal alleles of the Drosophila k43 gene result in smal
32                   We also identified several lethal alleles of the male sterile mutant, bobble (bob).
33  for genetic interactions with two recessive lethal alleles of zipper in a second-site noncomplementa
34 yprinidae), the average numbers of recessive lethal alleles per individual are 1.9 (95% confidence li
35 many individuals carry one or more recessive lethal alleles, posing an evolutionary conundrum for the
36  exons and splice sites for mutations in the lethal alleles qkl-1, qkkt1, qkk2, and qkkt3.
37 sses between F0 animals that carry embryonic lethal alleles recapitulate loss-of-function phenotypes,
38 ccurring and engineered sex-linked recessive lethal alleles (RLAs) to create sex separation strains f
39  the accumulation of strongly deleterious or lethal alleles, swamping the effect of any potentially a
40 es are distinct from those of two classes of lethal alleles (termed I and II) that show intergroup, i
41                 U. bromivora harbors a haplo-lethal allele that is linked to one mating type region.
42 a1) suppresses several temperature-sensitive lethal alleles that affect chromosome replication and ch
43 n defined by temperature-sensitive embryonic lethal alleles that strongly affect germline meiosis and
44 enomes) to generate three weaker, non-embryo-lethal, alleles (tps1-11, tps1-12 and tps1-13) and use t
45 s within the CRO1/She4p-like domain, and two lethal alleles were found to result from stop codon muta
46                       Unexpectedly, very few lethal alleles were identified, demonstrating the resili
47 tant plants from strong maternal gametophyte lethal alleles, which is not possible via conventional d
48  disrupting a target gene, forming recessive lethal alleles, while rescuing drive-carrying individual