ライフサイエンスコーパス: lemma

1 mental way through a complexity minimisation lemma.

2 anying the Rodl-Skokan hypergraph regularity lemma.

3 and Schacht succeeded in proving a counting lemma accompanying the Rodl-Skokan hypergraph regularity

4 teroskedasticity in quantitative traits, and LEMMA accounts for this by using robust standard error e

5 y, in some sections of the main veins in the lemma and glume, and in abaxial epidermis hair cells of

6 interaction of FUL2 with LHS1 could specify lemma and palea identity in the grass floret.

7 integuments (seed coat), the spikelet hull (lemma and palea) and the filial endosperm.

8 m1, expressed primarily in the outer organs (lemma and palea) that enclose developing florets and see

9 od for k-uniform hypergraphs, the regularity lemma and the counting lemma, have been obtained recentl

10 stem and also in determining the identity of lemmas and paleas; these two functions are separable, as

11 aploid subspecies of wheat with long glumes, lemmas, and grains.

12 ) result in gradual transitions of glumes to lemmas, and vice versa.

13 as modified petals and, possibly, palea and lemma as modified sepals.

14 Szemeredi's regularity lemma asserts that every graph can be decomposed into re

15 fferences in the relative expansion of awned lemma compartments can explain diversity in awn morpholo

16 ts, a putative prephonological signal (i.e., lemma) evoked by the object picture appears to have beco

17 rphism type, yielding the so-called counting lemma for graphs.

18 ation to a whole-genome regression approach (LEMMA) for estimating GxE heritability.

19 Awns, extensions of the bract-like lemma found in all grass inflorescences, are normally de

20 line references to Theorems, Definitions and Lemmas given in the main Article were incorrectly given

21 , and in abaxial epidermis hair cells of the lemma, glume, and rachis.

22 raphs, the regularity lemma and the counting lemma, have been obtained recently: Rodl and Skokan (bas

23 ecification of axillary floral meristems and lemma identity.

24 The counting lemma is proved by reducing the counting problem to a si

25 The lemma is then used to derive the Bayesian shrinkage esti

26 The combined application of these two lemmas is known as the regularity method for graphs and

27 nt height, more compact spikes, promotion of lemma-like characters in glumes and smaller lodicules.

28 eterminacy, with a large bouquet composed of lemma-like organs sprouting from the center of spikelets

29 where normal glumes enclose reiterated palea/lemma-like organs.

30 tamens into carpels and lodicules into palea/lemma-like structures.

31 The method is called LEMMA (Linear Environment Mixed Model Analysis) and esti

32 ff, hair-like structures which grow from the lemmas of wheat (Triticum aestivum) and other grasses th

33 LEMMA is more computationally efficient than LEMMA on large datasets, and produces results highly cor

34 gfp expression in coleoptiles, epicarps, and lemma/palea of developing spikes.

35 ticle bombardment, Gfp was expressed only in lemmas, paleas and awns of developing spikelets.

36 bristle-like structures extending from grass lemmas, provide protection against predators, contribute

37 An important lemma regarding the posterior mean of a normal likelihoo

38 ression of VRT2 resulted in leafy glumes and lemmas, reversion of spikelets to spikes, and downregula

39 These lemma-specific effects allow the spatiotemporal analysis

40 We discovered that awned lemmas that evolved independently share similarities in

41 mply, through an elementary "dual convexity" lemma, that s(alphaA + betaV) is also convex in alpha >

42 and Rodl) generalized Szemeredi's regularity lemma to k-uniform hypergraphs, and Nagle, Rodl, and Sch

43 es results highly correlated with those from LEMMA when applied to simulated data and real data from

44 strengthened by fulfillment of three logical lemmas which were extracted and assimilated in this work

45 e number of florets, each including a bract (lemma) with an axillary flower.