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1 tion for what is usually considered a highly polygenic trait.
2 the case in H. pylori, Mtz(r) might not be a polygenic trait.
3 adult height, a highly heritable and classic polygenic trait.
4 majority of human obesity is inherited as a polygenic trait.
5 Human height is a highly heritable, classic polygenic trait.
6 into the genetic architecture of this model polygenic trait.
7 Breast cancer risk is a polygenic trait.
8 o many autoimmune diseases is inherited as a polygenic trait.
9 D. sechellia and D. simulans appears to be a polygenic trait.
10 carcinoma susceptibility in the COP rat is a polygenic trait.
11 es over marker-assisted selection for highly polygenic traits.
12 tudies identified>1,000 genetic variants for polygenic traits.
13 Behaviors are often highly heritable, polygenic traits.
14 on of major gene(s) responsible for complex, polygenic traits.
15 ntly for simplifying the genetic analysis of polygenic traits.
16 be used to sensitize the genetic analysis of polygenic traits.
17 ingle-gene models are quite robust, even for polygenic traits.
18 We present a novel way to select for highly polygenic traits.
20 successful in identifying genes involved in polygenic traits and are valuable for crop improvement.
21 y be applied to GWA studies for other common polygenic traits and diseases, thus providing a new gene
23 ution is thought to be less likely in highly polygenic traits and distantly related species, this has
24 the genetic architecture of a set of related polygenic traits and the skeleton of the domestic dog (C
25 table hybrid strain that contains a complex, polygenic trait, and identifies new avenues for metaboli
26 on genetic variants that are associated with polygenic traits, and have typically been performed with
28 icate that human height is not only a highly polygenic trait, but also has high allelic heterogeneity
30 rmation can favor genetic analysis of highly polygenic traits, but not genome-wide prediction accurac
31 g of monogenic traits, genetic dissection of polygenic traits, construction of genome-wide physical m
32 at variation in the frequency of a heritable polygenic trait depends on spatial variation in two domi
35 effect, but unlike these other prototypical polygenic traits, genetic influence on anxiety is not we
37 within the Croatian data, and for the highly polygenic traits height and BMI when predicting into the
42 del the genetic architecture of quantitative polygenic traits in both the general European and the Fi
43 iphering the genetic architecture underlying polygenic traits in perennial species can inform molecul
45 ts to explore rare variants' contribution to polygenic traits, it is of great importance to character
46 alone for moderately complex but not highly polygenic traits measured in the maize nested associatio
47 the possibility remains that this is a truly polygenic trait or that multiple, rare variants contribu
49 Understanding the genetic architecture of polygenic traits requires investigating how complex netw
53 However, the evolutionary paths along which polygenic traits, such as size, evolve are poorly unders
56 hat autoantibody production in NZW mice is a polygenic trait that is influenced by contributions from
58 lelic heterogeneity is a frequent feature of polygenic traits, that comprehensive explorations of alr
59 roblem, we have used pigmentation as a model polygenic trait, three common human polymorphisms though
62 experimental model for the analysis of adult polygenic traits, we measured a mouse population for mul
63 mineral density is known to be a heritable, polygenic trait whereas genetic variants contributing to
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