ライフサイエンスコーパス: wing hair

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1 urn function as a group upstream of multiple wing hairs.

2 in the epithelium and differentiate abnormal wing hairs.

3 s two roles in the development of Drosophila wing hairs.

4 rmin Homology 3 (GBD-FH3) domain in Multiple Wing Hairs, a downstream component of the pathway sugges

5 m components including Inturned and Multiple Wing Hairs accumulate on the proximal side of wing cells

6 Wing hair alignment and ommatidial rotation, functional

7 ferentiation, and the expression of multiple wing hairs and DE-Cadherin.

8 Epithelial structures, such as the wing hairs and ommatidia in Drosophila, are aligned in t

9 The Fz6 phenotype strongly resembles the wing-hair and bristle patterning defects observed in Dro

10 /Dsh signalling that regulates the number of wing hairs, and blocks non-cell-autonomous repolarisatio

11 l vertex of each cell; in forming unbranched wing hairs; and in the correct positioning of veins and

12 ata argue that inturned, fuzzy, and multiple wing hairs are downstream components of the frizzled pat

13 phenotype of frizzled, inturned and multiple wing hairs are needed in the responding cells but not in

14 actin cytoskeleton to produce one actin-rich wing hair at the distal-most vertex of each cell.

15 strabismus and prickle, function to regulate wing hair, bristle and ommatidial polarity.

16 g is not only required in the manufacture of wing hairs, but also in the PCP read-out that directs wh

17 The polarity of Drosophila wing hairs displays remarkable fidelity.

18 ned regulates planar cell polarity (PCP) and wing hair formation in Drosophila wings.

19 ts; in the formation of a single actin-based wing hair from the distal vertex of each cell; in formin

20 wnstream genes inturned, fuzzy, and multiple wing hairs (inturned-like genes) and upstream genes such

21 tessellation model in which the alignment of wing hairs is dependent on cell shape and need not refle

22 We examined cytoskeleton formation during wing hair morphogenesis using both confocal and electron

23 candidate genes that functioned in wing and wing hair morphogenesis.

24 Wing hairs mostly preferred reversed airflow, which occu

25 ue that in the Drosophila epidermis multiple wing hairs (mwh) acts as a downstream component of the p

26 The downstream PCP gene multiple wing hairs (mwh) plays a key role in this process and ac

27 Here we describe the role of Multiple Wing Hairs (Mwh), a novel formin homology 3 (FH3)-domain

28 tion pathway disrupt tissue polarity; on the wing, hairs normally point distally but their polarity i

29 simultaneously mutant for inturned, multiple wing hairs, or dishevelled but it was blocked when the e

30 ing was mutant for inturned, fuzzy, multiple wing hairs, or dishevelled.

31 in the inturned (in) gene result in abnormal wing hair polarity and in many wing cells forming two or

32 cle formation and pigmentation, and abnormal wing hair polarity.

33 ommatidia formation in the compound eye, and wing hair polarization.

34 We found inturned, fuzzy, and multiple wing hairs were required for a gradient of frizzled, sta

35 n parallel with the Fz/PCP effector multiple wing hairs, which restricts prehair formation along the

36 lso in the PCP read-out that directs where a wing hair will be secreted.

37 irectional sensitivity to stimulation of the wing hairs with low-speed airflow.

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