ライフサイエンスコーパス: tarsus

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1 he fly tibia also exhibits a fused tibia and tarsus.

2 n from an ancestral limb with an unsegmented tarsus.

3 distal axis: a proximal segment and a distal tarsus.

4 location in fornix (2% vs 6%, P = .0016) and tarsus (1% vs 4%, P = .0018), larger median basal diamet

5 rotein diets had reduced growth rates of the tarsus and delayed emergence of the 9th primary.

6 quired for the elaboration of pattern in the tarsus and its effects suggest a progressive model for t

7 ds to the distal-most region of the leg, the tarsus and the distal tibia.

8 nes accumulates in nuclei in the presumptive tarsus and the inter-joints of proximal leg segments and

9 y in the retina and CYP2J19B in the beak and tarsus and to a variable extent in the retina.

10 ction, with an adducted hallux, an elongated tarsus, and derived ankle and calcaneocuboid joints.

11 atory receptor neurons of the labial palpus, tarsus, and wing anterior margin, but not in olfactory r

12 ted levator aponeurosis onto to the superior tarsus approximate that aspect of native anatomic featur

13 ormally expressed in the central part of the tarsus domain but expands into distal and proximal regio

14 r and the LIM-domain binding protein Chip in tarsus four, and between Al, Lim1 and Chip in the pretar

15 conjunctiva in 31 (97%), fornix in 9 (28%), tarsus in 3 (9%), semilunar fold in 10 (31%), and carunc

16 levator aponeurosis attached to the anterior tarsus in both groups.

17 nes are expressed in distinct regions of the tarsus, including aristaless (al) and lim1 in the pretar

18 The distal region of the Drosophila leg, the tarsus, is divided into five segments (ta I-V) and termi

19 However, male mass and tarsus length showed no genetic correlation between week

20 The body size traits of mass and tarsus length were genetically correlated with each othe

21 ponent analysis (wing, culmen, head+bill and tarsus length).

22 specific relationships between telomeres and tarsus length, potentially reflecting differential costs

23 Across the presumptive tarsus, lines modulates the opposing expression landscap

24 or and inferior areas of bulbus, fornix, and tarsus of male Sprague-Dawley rats (n = 6).

25 nd lower fornix bilaterally and involved the tarsus of the right upper lid.

26 ketocarotenoids were absent in the beak and tarsus of yellowbeak birds.

27 in the wing and the segmentation of the leg tarsus (reviewed in [7-9]).

28 In the tarsus, ss is expressed only early, and is required for

29 gments and creates a chimeric nub-RNAi tibia-tarsus that retains a tibial identity in its proximal ha

30 Newer surgical treatments aim to preserve tarsus to improve eyelid stability and position.

31 tterning alterations in patella and proximal tarsus, to more closely resemble the corresponding forel

32 rtical blepharotomy through which a strip of tarsus was removed.

33 The tarsus, which has been proposed to be an ancestral struc

34 cation of the segments and annulation in the tarsus, while poorly developed thoracic wing pads sugges

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