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1 nforced the multilayered architecture of the cotton fiber.
2 ould lead to novel ways to engineer superior cotton fiber.
3 nanoparticles throughout an entire volume of cotton fiber.
4 elongation, such as occurs in the developing cotton fiber.
5 ful in genetic engineering schemes to modify cotton fiber.
6 e cellulose biosynthesis stage in developing cotton fibers.
7 on species producing over 90% of the world's cotton fibers.
8 for alternative mRNA isoforms in developing cotton fibers.
9 een microtubules and actin microfilaments in cotton fibers.
10 aments, but never with axial actin cables in cotton fibers.
11 lpha-tubulin transcript levels in elongating cotton fibers.
12 ial sequencing of anonymous cDNA clones from cotton fibers.
13 ndary wall cellulose synthesis in developing cotton fibers.
14 ormal development or structural integrity of cotton fibers.
16 h seed, which helps explain how thousands of cotton fibers achieve their great length within a confin
19 ic immunolocalization of sucrose synthase in cotton fibers, and phylogenetic relationships between ce
20 characterization of rapid cell elongation in cotton fibers, approximately 14,000 unique genes were as
24 decreased from 3 to 8-DPA in the developing cotton fiber cells while transcript levels remained low.
26 nd specific activities on pectic material in cotton fibers compatible with their use in the scouring
28 eld emission-scanning electron microscopy of cotton fibers developing in situ within the boll demonst
29 the potential regulatory roles of miRNAs in cotton fiber development and the importance of miRNAs in
32 ta indicate significant roles of laccases in cotton fiber development, and presents an excellent oppo
33 ription factors are likely to play a role in cotton fiber development, the molecular evolutionary pro
34 istribution of gene networks responsible for cotton fiber development, we investigated the distributi
40 highly expressed in the elongation stages of cotton fiber differentiation, suggesting a role of this
41 n factor genes are specifically expressed in cotton fiber during different developmental stages, incl
43 sA1 ZnBD is rapidly degraded when exposed to cotton fiber extracts, whereas the oxidized dimer is res
44 em indicates that the N-terminal portions of cotton fiber GhCesA1 and GhCesA2 containing these domain
45 present work, we show that the half-life of cotton fiber GhCesA1 protein is <30 min in vivo, far les
47 This observation suggests that in developing cotton fibers, increased mitochondrial sublimon replicat
48 n wildtype Xu-142, 26 miRNAs are involved in cotton fiber initiation and 48 miRNAs are related to pri
50 Among 54 miRNAs, 18 miRNAs were involved in cotton fiber initiation and eight miRNAs were related to
55 orld's dominant renewable textile fiber, and cotton fiber is valued as a research model because of it
56 s been developed that introduces copper into cotton fibers, latex, and other polymeric materials.
58 the superior yield and quality of tetraploid cotton fibers may be explained by accelerated Dt to At c
60 ast two-hybrid system to identify a putative cotton fiber metallothionein and to confirm it as a prot
62 sms that govern developmental programming of cotton fiber morphogenesis in these two cultivated speci
63 cell, using as a model the seed trichomes ("cotton fiber") of allopolyploid (containing "A" and "D"
67 and distinct supramolecular structure of the cotton fiber provided a favorable environment for the co
71 New data are included on phosphorylation of cotton fiber sucrose synthase, possible regulation by Ca
72 be encouraged to 'self-fumigate' nests with cotton fibers that have been treated with permethrin.
75 are responsible for cellulose production in cotton fiber, very limited numbers of GhCesA genes have
76 ivity and biochemical analysis of developing cotton fibers was performed using G. arboreum species.
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