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1                       Orthologous genes from monocotyledonous and dicotyledonous C(3) species also co
2 accumulates during early seed development in monocotyledonous and dicotyledonous flowering plants.
3 istant APs, variation potentials, and SPs in monocotyledonous and dicotyledonous plant species (Horde
4 ction in the regulation of flowering time in monocotyledonous and dicotyledonous plants, but also unv
5 ting anther-specific gene expression in both monocotyledonous and dicotyledonous plants, pointing to
6 ion with endogenous proteins in a variety of monocotyledonous and dicotyledonous plants, suggesting b
7 rming the significance of methylomes in both monocotyledonous and dicotyledonous species.
8 port that an NLR immune receptor (MLA1) from monocotyledonous barley is fully functional in partially
9 erimental analysis of the MRP subfamily in a monocotyledonous crop plant.
10 g mechanisms is still limited, especially in monocotyledonous crop plants.
11 than 400 homologs, representing 26 genera of monocotyledonous, dicotyle-donous and one coniferous spe
12 dicotyledonous species yet distinct from the monocotyledonous grass species, Oryza sativa.
13  based on barley stripe mosaic virus, in the monocotyledonous host barley.
14                                           In monocotyledonous leaves, GA controls growth by regulatin
15                     An oleosin gene from the monocotyledonous maize (Zea mays L.) was transferred int
16                      The results show that a monocotyledonous oleosin possesses sufficient targeting
17            This first crystal structure of a monocotyledonous PAL displayed a unique conformation in
18            Sequence comparison of CCaMK from monocotyledonous plant (lily) and dicotyledonous plant (
19 ginal alc gene switch was ineffective in the monocotyledonous plant sugar cane, and describe a modifi
20 resents the first DHFR-TS gene cloned from a monocotyledonous plant.
21            In most NAS of dicotyledonous and monocotyledonous plants (class Ia and Ib), the core-NAS
22 ased on the analysis of related sequences in monocotyledonous plants an alternative classification of
23 important superfamily of regulatory genes in monocotyledonous plants and reveals a novel function for
24               Progress with this approach in monocotyledonous plants is limited so far by the availab
25                        Duckweeds are aquatic monocotyledonous plants of potential economic interest w
26                    Genetic transformation of monocotyledonous plants still presents a challenge for p
27 petitive sequences, of which the bulbous and monocotyledonous plants tulip and lily are examples.
28  orthologs of HQT in switchgrass or in other monocotyledonous plants with complete genome sequences.
29 r the purposes of gene expression or VIGS in monocotyledonous plants, and among these, the tripartite
30 ins are found in all dicotyledonous and some monocotyledonous plants, but additional crystalloid P-pr
31   Rice (Oryza sativa) is a model species for monocotyledonous plants, especially for members in the g
32 widely applicable to both dicotyledonous and monocotyledonous plants, especially those varieties that
33               In the developing endosperm of monocotyledonous plants, starch granules are synthesized
34 tile gene switch is functional in transgenic monocotyledonous plants, which include some of the most
35  acquired resistance is poorly understood in monocotyledonous plants.
36 tant model species for the Poaceae and other monocotyledonous plants.
37 rted from rice, which is a model species for monocotyledonous plants.
38 s for a major group of flowering plants, the monocotyledonous plants.
39 onent in dicotyledonous and non-graminaceous monocotyledonous plants.
40  of hosts, including both dicotyledonous and monocotyledonous plants.
41 utagenesis in several dicotyledonous and few monocotyledonous plants.
42 sm both in dicotyledonous tobacco plants and monocotyledonous rice cells.
43                     However, the capacity of monocotyledonous rice to recognize flagellins of key ric
44 onous Arabidopsis thaliana and 50% less than monocotyledonous rice.
45 rate assimilation in both dicotyledonous and monocotyledonous species depends on photorespiration.
46 milies together with the GS genes from other monocotyledonous species form four distinct clades.
47 nsgene expression in all organs of the model monocotyledonous species rice (Oryza sativa L. cv. Nippo
48 deae belongs to a different order than other monocotyledonous species that have been sequenced and co
49 ic module seems to be conserved in dicot and monocotyledonous species to prevent branching under ligh
50 ily of genes has functionally evolved in the monocotyledonous species wheat (Triticum aestivum).
51 le, with an average of -140 per thousand for monocotyledonous species, -107 per thousand for dicotyle
52 for the use of negative selection markers in monocotyledonous species.
53                                     The four monocotyledonous taxa with the highest number of seeds c