ライフサイエンスコーパス: unsegmented

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1 es into rhombomeres, the spinal cord remains unsegmented.

2 e in nature has always been characterized as unsegmented.

3 In severe cases embryos appear unsegmented.

4 uniform Wingless activity are added back to unsegmented embryos (wingless- engrailed-).

5 Unsegmented embryos are much shorter than wild type.

6 (Jingmenvirus) related to the prototypically unsegmented Flaviviridae.

7 Lox22-Otx RNA is primarily restricted to an unsegmented head domain, including tissues in the foregu

8 n peripheral ectoderm or endoderm, or in the unsegmented head region (prostomium).

9 During segmentation of vertebrate embryos, unsegmented mesenchymal mesoderm is divided into epithel

10 e neural tube, and dramatically expanded the unsegmented mesenchymal PSM while blocking somitogenesis

11 tebrates have a relatively extensive zone of unsegmented mesenchyme (i.e., presomitic mesoderm) inter

12 The unsegmented, mud-dwelling echiuran spoon worms and the g

13 The cells exhibit unsegmented nuclei, have Gr-1(dim)Ly-6G(dim)CD11b(+) phe

14 that was either coextensive with the target (unsegmented) or appeared segmented from it due to a gap

15 5-6 embryos and subsequently in somites and unsegmented paraxial and lateral plate mesoderm overlapp

16 anisms the gene is specifically expressed in unsegmented paraxial mesoderm and its immediate progenit

17 -helix transcription factor expressed in the unsegmented paraxial mesoderm and throughout epithelial

18 ecause when pieces of dorsal neural tube and unsegmented paraxial mesoderm are combined in tissue cul

19 analysis of lunatic fringe expression in the unsegmented paraxial mesoderm of chick embryos.

20 ntation in vertebrates first arises when the unsegmented paraxial mesoderm subdivides to form paired

21 ically expressed in developmentally immature unsegmented paraxial mesoderm, causes complete failure o

22 Both genes are transcribed in the unsegmented presomitic mesoderm (PSM), newly formed somi

23 ls cyclic initiation of transcription in the unsegmented presomitic mesoderm (PSM).

24 ective somites cause them to detach from the unsegmented presomitic mesoderm [1-3].

25 ntrols the periodic cleavage of somites from unsegmented presomitic mesoderm during vertebrate segmen

26 tation clock') intrinsic to the cells in the unsegmented presomitic mesoderm, and is manifested in cy

27 Somites form by an iterative process from unsegmented, presomitic mesoderm (PSM).

28 Importantly, the unsegmented region does not generate additional tissue v

29 With unsegmented retinal angiograms, the sensitivity and spec

30 nce space by a viral genome (in this case an unsegmented RNA) can reach a point of the space in which

31 nsion of the hindbrain at the expense of the unsegmented spinal cord.

32 Segmentations of 36 further unsegmented target images of developing brains yielded v

33 d have arisen from an ancestral limb with an unsegmented tarsus.

34 ern of double segment periodicity in overtly unsegmented tissue.

35 ves of clock gene expression sweeping in the unsegmented tissue.

36 scillatory Her1 protein production along the unsegmented tissue.

37 segmented vertebral column as well as other unsegmented tissues.

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