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1 rpret geographic patterns of isolation among Z. mays subspecies considering these findings and sugges
2   Intraspecific diversity at chiB, chiI, and Z. mays ssp. parviglumis chiA are consistent with a neut
3 g the lncRNAs of A. thaliana, O. sativa, and Z. mays, respectively.
4 plotypes (from Z. mays spp. mexicana Chalco, Z. mays spp. parviglumis, and Z. luxurians) and a common
5                               In C. elegans, Z. mays, D. melanogaster, D. simulans and H. sapiens, al
6 protects actin filaments in these cells from Z. mays profilin (ZmPRO5)-induced depolymerization, in a
7 ly distinct teosinte A1 Sh2 haplotypes (from Z. mays spp. mexicana Chalco, Z. mays spp. parviglumis,
8 ched plasma membrane fractions isolated from Z. mays leaves with an apparent K(d) of 1.3 nM and a Hil
9  plant growth, the question arises as to how Z. mays produces high levels of zealexins without negati
10                                           In Z. mays Merit we conclude that phytochrome is the sole p
11 atural metabolite of indole-3-acetic acid in Z. mays seedlings.
12 sive characterization of leaf delta(13) C in Z. mays.
13 tion and evolution of the fps gene family in Z. mays enabled it to produce dedicated FPSs for develop
14 hree farnesyl diphosphate synthases (FPS) in Z. mays and examined the resultant impacts on different
15 e strong support for a CO2 response of gm in Z. mays, and indicate that gm in maize is probably drive
16 peculiarity of cultivation nor inbreeding in Z. mays.
17 nt phenotypes, including ones nonexistent in Z. mays.
18                       Analysis of repeats in Z. mays and other species (Zea diploperennis, Zea luxuri
19 umber of studies have explored this trait in Z. mays.
20 iglumis) was domesticated into modern maize (Z. mays ssp. mays).
21 d defense could contribute to the ability of Z. mays to produce high levels of phytoalexins without n
22       We defined core sets of collections of Z. mays ssp. mexicana and ssp. parviglumis that attempt
23  diversity (32% of the level of diversity of Z. mays ssp. parviglumis).
24                             Hybridization of Z. mays genomic BAC clones with the pac1 sequence identi
25    We found that upon U. maydis infection of Z. mays, KWL1-b is expressed at significantly lower leve
26 f delta(13) C exists across diverse lines of Z. mays, which we show to be heritable across several en
27 iption, correct a segment of the sequence of Z. mays chloroplasts and D. melanogaster LSU RNA, correl
28 fferentially distributed across the walls of Z. mays stomatal complexes.
29 o the tb1 cDNA confer pleiotropic effects on Z. mays morphology.
30 viglumis, Z. mays mexicana, and particularly Z. mays huehuetenangensis.
31  and its wild relatives Z. mays parviglumis, Z. mays mexicana, and particularly Z. mays huehuetenange
32 ions of teosinte (Zea mays ssp. parviglumis, Z. mays ssp. mexicana, and Z. diploperennis).
33 representing maize, its presumed progenitor (Z. mays ssp. parviglumis), and a more distant relative (
34 e (Zea mays ssp. mays), its wild progenitor (Z. mays ssp. parviglumis), a more distant species within
35 s, five populations of the maize progenitor, Z. mays ssp. parviglumis, six other Zea populations, and
36  centromeres in maize and its wild relatives Z. mays parviglumis, Z. mays mexicana, and particularly
37 espond to the previously defined subspecies, Z. mays ssp. parviglumis and ssp. mexicana, although the
38 n Tripsacum dactyloides, maize and teosinte (Z. mays ssp. parviglumis).
39  subsp mays) was domesticated from teosinte (Z. mays subsp parviglumis) through a single domesticatio
40 ays) from its wild ancestors, the teosintes (Z. mays ssp. parviglumis and mexicana).
41                                          The Z. mays cDNA clone contains an open reading frame encodi
42 t structural variations are pervasive in the Z. mays genome and are enriched at loci associated with
43       When placed under GALA regulation, the Z. mays cDNA functionally complemented the erg6 mutation
44  (AtHCX1) is 77% identical to CAX1 while the Z. mays homolog of CAX (ZmHCX1) is 64% identical to CAX1
45 se (10-40 degrees C) of C4 gm in S. viridis, Z. mays and Miscanthus x giganteus.
46 , inverted state is present only in the wild Z. mays subspecies parviglumis and mexicana and is compl
47  at a low level and appears most common with Z. mays ssp. mexicana.
48                               Cytolines with Z. mays teosinte cytoplasms were generally indistinguish
49                   Results show that ZmEXPB6 (Z. mays beta-expansin 6) protein is lacking in growth-in