ライフサイエンスコーパス: etioplast

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1 oplasts) versus the yellow base of the leaf (etioplasts).

2 s localized to the prolamellar bodies within etioplasts.

3 component of metabolism and redox sensing in etioplasts.

4 f large amounts of Pchlide b in the isolated etioplasts.

5 es, including chloroplasts, amyloplasts, and etioplasts.

6 ytochrome f, and in protein targeting in the etioplast, a nonphotosynthetic plastid type.

7 Mutant seedlings also display defects in etioplast and amyloplast development.

8 4VCR is a membrane-bound enzyme, embedded in etioplast and etiochloroplast membranes.

9 aracterized by smaller prolamellar bodies in etioplasts and decreased thylakoid stacking in chloropla

10 -kDa immunoreactive protein were detected in etioplasts, and no immunoreactive proteins were observed

11 (Pchlide) b is an abundant pigment in barley etioplasts but is rather unstable, as it is rapidly conv

12 mediating the transcriptional output during etioplast-chloroplast transition.

13 in various types, which include proplastids, etioplasts, chloroplasts, amyloplasts, and chromoplasts.

14 n the cue mutants, which correlates with the etioplast defect.

15 ishes a quantitative requirement for PORA in etioplast development by demonstrating significant membr

16 rtant for skotomorphogenesis by assisting in etioplast development, and normal photomorphogenic devel

17 l chloroplast differentiation and absence of etioplast development.

18 oprotective activities required to poise the etioplast for light development.

19 0-fold purification of P Phi B synthase from etioplasts from dark-grown oat (Avena sativa L. cv Garry

20 Moreover, the high pleomorphy of etioplasts from dark-grown seedlings, leucoplasts from r

21 rexpression also promotes the development of etioplasts from proplastids in dark-grown seedlings, sub

22 ght-induced development of chloroplasts from etioplasts in Arabidopsis (Arabidopsis thaliana).

23 amellar bodies (PLBs) and the development of etioplasts in darkness.

24 o green seedlings involves the conversion of etioplasts into mature chloroplasts via a multifaceted,

25 n etiolated barley leaves or isolated barley etioplasts irrespective of the extraction protocol.

26 lles, and that it plays an essential role in etioplast metabolism by participating in the desaturatio

27 show that the redox state of the PQ pool in etioplasts might control chlorophyll biosynthesis, perha

28 to gain insight into the function of PTOX in etioplasts of dark-grown seedlings.

29 cialized plastid types, such as proplastids, etioplasts, or amyloplasts.

30 st that they define a respiratory process in etioplasts that we have termed "etiorespiration".

31 RNA accumulation, and the differentiation of etioplasts to chloroplasts, are retarded in their abilit

32 tructural membrane transformation during the etioplast-to-chloroplast transition in runner bean (Phas

33 trastructural changes characteristic for the etioplast-to-chloroplast transition.

34 also been claimed that extraction of barley etioplasts with 100% acetone containing 0.1% diethyl pyr

35 The mutants have underdeveloped etioplasts, with increasing impairments in cue6, cue8 an

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