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1 olved relatively recently and only a few are heteromorphic.
2 t the threespine stickleback Y chromosome is heteromorphic and has suffered both inversions and delet
3            In many taxa, sex chromosomes are heteromorphic and largely non-recombining.
4 ytologically homomorphic sex chromosomes are heteromorphic at the molecular level.
5  Therefore, br is necessary for the mutable (heteromorphic) changes that occur during hemimetabolous
6  be simultaneously present in a structurally heteromorphic chromatin fiber with uniform 30 nm diamete
7 from standard animal models in that it lacks heteromorphic chromosomes (instead, sex determination is
8 ean fruits on an individual plant, and these heteromorphic diaspores give rise to plants that differ
9 3:1, and 1:3, evidence of perfect duplex and heteromorphic duplex complexes is found in all cases.
10 es, the sequence dependent features of these heteromorphic duplex states and their thermodynamic stab
11      This is indicative of a melting hybrid, heteromorphic duplex states formed from two nonperfectly
12 ed, TRD was present only in those inheriting heteromorphic dyads.
13                                              Heteromorphic flower development in Primula is controlle
14                               Development of heteromorphic flowers is coordinated by genes at the S l
15                                              Heteromorphic hybrid duplex DNA complexes are duplex sta
16 autosomal block of heterochromatin, which is heteromorphic in 6-8% of humans, whereas pericentric inv
17  this chromosomal pair is characteristically heteromorphic in a broad range of organisms.
18               Purification of these enlarged heteromorphic lamellar structures by buoyant density cen
19 nation demonstrated the presence of enlarged heteromorphic lamellar structures undergoing degeneratio
20 d some plasticity such as the development of heteromorphic leaves and well-developed roots system.
21 twork shifted towards geographically closer, heteromorphic male neighbour associations.
22 lds have been hybridized to create the novel heteromorphic nucleoside 5-(2-amino-3-cyano-5-oxo-5,6,7,
23 s the pathways of folding of three different heteromorphic pairs, displaying increasingly high-sequen
24    We propose an evolutionary model in which heteromorphic pericentromeric repeat structures such as
25                 Because collagen type V is a heteromorphic protein in which molecules may be composed
26                   Because the homologous but heteromorphic proteins are identical at most positions i
27   We describe the design of these homologous heteromorphic proteins, their structural properties as d
28                                          The heteromorphic regions of chromosomes 1, 9, 15, 16, and Y
29    Differences in the DAPI lifetimes for the heteromorphic regions suggest differences in the structu
30 ics of ancestral functional and structurally heteromorphic S haplotypes or resulting from decay conco
31 ed by both a translocation event between the heteromorphic satellite regions of chromosomes 14 and 15
32  fish (Gasterosteus aculeatus) do not have a heteromorphic sex chromosome pair, although recent genet
33 n intermediate pattern compared to taxa with heteromorphic sex chromosomes and taxa without sex chrom
34 f this finding in regard to the evolution of heteromorphic sex chromosomes and the mechanisms that en
35                           Unique features of heteromorphic sex chromosomes are produced as a conseque
36                                              Heteromorphic sex chromosomes are thought to represent a
37 in species with homomorphic sex chromosomes, heteromorphic sex chromosomes are thought to represent a
38 otype is a key factor: Smaller autosomes and heteromorphic sex chromosomes become weak links when DSB
39                                       As the heteromorphic sex chromosomes evolved from a pair of aut
40                             The evolution of heteromorphic sex chromosomes has repeatedly resulted in
41                                              Heteromorphic sex chromosomes have originated independen
42 chromosomes in boas (Boidae), but completely heteromorphic sex chromosomes in both garter snakes (Col
43                        Our data suggest that heteromorphic sex chromosomes in males (that is, a hyper
44                    Recombination in ancient, heteromorphic sex chromosomes is typically suppressed at
45 sex chromosomes, Viperidae having completely heteromorphic sex chromosomes, and Colubridae showing pa
46                                              Heteromorphic sex chromosomes, such as the X/Y pair in m
47           The mosquito Anopheles gambiae has heteromorphic sex chromosomes, while the mosquito Aedes
48 female individuals) and has a pair of highly heteromorphic sex chromosomes, with XY males.
49  segregating at a single locus, sometimes on heteromorphic sex chromosomes.
50 motion the evolutionary processes generating heteromorphic sex chromosomes.
51 sex-determining factors in species that lack heteromorphic sex chromosomes.
52   Silene latifolia is a dioecious plant with heteromorphic sex chromosomes.
53 ination in Silene latifolia is controlled by heteromorphic sex chromosomes.
54 ammals and many insects, determine sex using heteromorphic sex chromosomes.
55            One involves physically distinct (heteromorphic) sex chromosomes (X and Y, or Z and W) tha
56  plants do not have cytologically different (heteromorphic) sex chromosomes.
57 hic gametophytic, homomorphic sporophytic or heteromorphic SI.
58 sion screening, which guarantee formation of heteromorphic superbeads-on-a-string structures that com
59 on of the Y chromosomes in many species with heteromorphic X/Y chromosomes.
60 n homomorphic sex chromosomes, and show that heteromorphic ZW chromosomes in rattlesnakes lack chromo
61 aracidium gomesi, a species with conspicuous heteromorphic ZW/ZZ sex chromosomes.

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