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1 storage molecule) in the stem (a long-term C storage organ).
2 perm to the female's spermathecae (long-term storage organs).
3 gold standard because the liver is the major storage organ.
4 te metabolism, consistent with its role as a storage organ.
5 vegetables, and plants producing underground storage organs.
6 h of new vegetative tissues, seeds, or other storage organs.
7 ng to the normal localization of SP to sperm-storage organs.
8 e lumen of the uterus and the female's sperm storage organs.
9 sperm and Acp36DE to a limited area near the storage organs.
10 e female, and in only one of her three sperm-storage organs.
11 rmatozoa and is retained in the female sperm storage organs.
12 t (FRT), such as a uterus, glands, and sperm storage organs.
13 pathways exclusive to epiphytic species with storage organs.
15 s shown they have evolved two separate sperm storage organs, allowing them to make post-copulatory pa
16 esulting in marked reduction of sperm in the storage organs and decreased fecundity, whereas enhancem
17 ly in vacuolar membranes of cotyledons (seed storage organs) and is synthesized during seed maturatio
22 onal climates invest carbon into belowground storage organs (e.g. rhizomes) to support growth when ph
24 e, stems elongate at the expense of leaf and storage organ expansion, branching is inhibited, and flo
25 needed for the accumulation of sperm in the storage organs, fail to complete the full sequence of th
26 this role, Acp29AB localizes to female sperm storage organs following mating, although it does not ap
27 e once considered the adipocyte as a passive storage organ for efficient storage of long-term energy
28 photosynthetic tissues and within dedicated storage organs has been characterized extensively in man
30 ind that specialized cell types in the sperm storage organs heavily invest in expressing SFP genes.
31 opersicum) fruits representing heterotrophic storage organs important for agriculture and human diet.
33 of the three-dimensional structure of sperm storage organs in any vertebrate to the best of our know
34 d manipulation of carbon partitioning within storage organs in favour of starch synthesis, and attemp
37 n heterotrophic tissues other than dedicated storage organs is poorly characterized, and its function
40 enes to elucidate how sperm and female sperm-storage organ length co-evolved into one of nature's mos
41 d for divergent sperm length or female sperm-storage organ length, we experimentally show that male f
42 ted with the rapid evolution of female sperm-storage organ morphology and corresponding sperm quality
43 ace in the female, and by which female sperm-storage organ morphology biases fertilization in favour
44 ing interval, progeny production rate, sperm-storage organ morphology, and a number of sperm performa
45 in the fat body, the major immune and lipid storage organ of the fruit fly, Drosophila melanogaster,
51 eir glycocalyx is shed in the female's sperm storage organs, sperm transition from a period of dorman
52 xtended lifespan of sperm within the queen's storage organ (the spermatheca) after mating is largely
53 co modeling predicted that, in the two grain storage organs (the endosperm and embryo), the light-ind
54 The length of the female's primary sperm-storage organ, the seminal receptacle, has undergone rap
55 lives and must use sperm stored in the sperm storage organ, the spermatheca, to fertilize a lifetime'
57 the fate of sperm inside the female's sperm storage organs, to quantify sperm competition, and to as
59 has been hypothesized that plant underground storage organs (USOs) played key roles in the initial ho
61 ption that circulating factors released from storage organs were able to signal bodily energy reserve