ライフサイエンスコーパス: Z. mays

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1 Intraspecific diversity at chiB, chiI, and Z. mays ssp. parviglumis chiA are consistent with a neut

2 plotypes (from Z. mays spp. mexicana Chalco, Z. mays spp. parviglumis, and Z. luxurians) and a common

3 protects actin filaments in these cells from Z. mays profilin (ZmPRO5)-induced depolymerization, in a

4 ly distinct teosinte A1 Sh2 haplotypes (from Z. mays spp. mexicana Chalco, Z. mays spp. parviglumis,

5 ched plasma membrane fractions isolated from Z. mays leaves with an apparent K(d) of 1.3 nM and a Hil

6 In Z. mays Merit we conclude that phytochrome is the sole p

7 atural metabolite of indole-3-acetic acid in Z. mays seedlings.

8 e strong support for a CO2 response of gm in Z. mays, and indicate that gm in maize is probably drive

9 peculiarity of cultivation nor inbreeding in Z. mays.

10 nt phenotypes, including ones nonexistent in Z. mays.

11 Analysis of repeats in Z. mays and other species (Zea diploperennis, Zea luxuri

12 iglumis) was domesticated into modern maize (Z. mays ssp. mays).

13 We defined core sets of collections of Z. mays ssp. mexicana and ssp. parviglumis that attempt

14 diversity (32% of the level of diversity of Z. mays ssp. parviglumis).

15 Hybridization of Z. mays genomic BAC clones with the pac1 sequence identi

16 iption, correct a segment of the sequence of Z. mays chloroplasts and D. melanogaster LSU RNA, correl

17 o the tb1 cDNA confer pleiotropic effects on Z. mays morphology.

18 viglumis, Z. mays mexicana, and particularly Z. mays huehuetenangensis.

19 and its wild relatives Z. mays parviglumis, Z. mays mexicana, and particularly Z. mays huehuetenange

20 ions of teosinte (Zea mays ssp. parviglumis, Z. mays ssp. mexicana, and Z. diploperennis).

21 representing maize, its presumed progenitor (Z. mays ssp. parviglumis), and a more distant relative (

22 e (Zea mays ssp. mays), its wild progenitor (Z. mays ssp. parviglumis), a more distant species within

23 s, five populations of the maize progenitor, Z. mays ssp. parviglumis, six other Zea populations, and

24 centromeres in maize and its wild relatives Z. mays parviglumis, Z. mays mexicana, and particularly

25 espond to the previously defined subspecies, Z. mays ssp. parviglumis and ssp. mexicana, although the

26 n Tripsacum dactyloides, maize and teosinte (Z. mays ssp. parviglumis).

27 subsp mays) was domesticated from teosinte (Z. mays subsp parviglumis) through a single domesticatio

28 ays) from its wild ancestors, the teosintes (Z. mays ssp. parviglumis and mexicana).

29 The Z. mays cDNA clone contains an open reading frame encodi

30 t structural variations are pervasive in the Z. mays genome and are enriched at loci associated with

31 When placed under GALA regulation, the Z. mays cDNA functionally complemented the erg6 mutation

32 (AtHCX1) is 77% identical to CAX1 while the Z. mays homolog of CAX (ZmHCX1) is 64% identical to CAX1

33 se (10-40 degrees C) of C4 gm in S. viridis, Z. mays and Miscanthus x giganteus.

34 , inverted state is present only in the wild Z. mays subspecies parviglumis and mexicana and is compl

35 at a low level and appears most common with Z. mays ssp. mexicana.

36 Cytolines with Z. mays teosinte cytoplasms were generally indistinguish

37 Results show that ZmEXPB6 (Z. mays beta-expansin 6) protein is lacking in growth-in

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