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1 hite areas have small plastids that resemble proplastids.
2 seedlings have plastids which also resemble proplastids.
5 comparisons with proteomes of unfractionated proplastids and chloroplasts facilitated the determinati
6 diating the development of chloroplasts from proplastids and enhancing chloroplast growth and divisio
7 mes of highly enriched nucleoid fractions of proplastids and mature chloroplasts isolated from the ma
8 has been believed that the SAM contains only proplastids and that these become chloroplasts only in t
10 During this transition, promitochondria and proplastids develop into mature organelles and their DNA
13 d was observed in peroxisomes, mitochondria, proplastids, endoplasmic reticulum, cytoplasmic or perib
14 They exist in various types, which include proplastids, etioplasts, chloroplasts, amyloplasts, and
18 promotes the development of etioplasts from proplastids in dark-grown seedlings, subsequently enhanc
19 e globular stage of embryo development, when proplastids in normal embryos differentiate and acquire
20 of the ubiquitous expression of DCL and the proplastid-like appearance of dcl-affected plastids, the
21 carrots) containing chromoplasts, and 53% in proplastids of cultured cells when compared to chloropla
22 ndle sheath cell fate is determined, and the proplastids of each differentiate into the dimorphic chl
23 process that triggers the differentiation of proplastids or other noncolored plastids into chromoplas
27 enome, and the developmental transition from proplastid to chloroplast is regulated by nuclear genes.
29 opment from hundreds of genome copies in the proplastid to undetectable levels in the mature chloropl
31 scribes the transition of non-photosynthetic proplastids to photosynthetically active chloroplasts in
32 Chloroplasts of higher plants develop from proplastids, which are undifferentiated plastids that la