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1 ct classes of polymerase to synthesize their exoskeleton.
2 walking can be reduced by an unpowered ankle exoskeleton.
3 olts, during which the animal produces a new exoskeleton.
4 windows (12- to 350-microm diameters) in the exoskeleton.
5 the partial degradation of the overlying old exoskeleton.
6 or the indirect flight muscles (IFMs) to the exoskeleton.
7 ntimately linked to remodeling the cell wall exoskeleton.
8 ating in emergence of an insect from its old exoskeleton.
9 ble and hardens and darkens the color of the exoskeleton.
10 esis, and potential contributions to the new exoskeleton.
11 he major component of the nematode cuticular exoskeleton.
12 eposition in fungal cell walls and arthropod exoskeletons.
13 al cell walls, crustacean shells, and insect exoskeletons.
14 a major component of fungal walls and insect exoskeletons.
15 wth, insects must periodically replace their exoskeletons.
16 agenous extracellular matrix which forms the exoskeleton and defines the shape of the worm.
17 re also associated with abnormalities in the exoskeleton and improper development of the epidermis.
18  mechanism for survival: A mosquito's strong exoskeleton and low mass renders it impervious to fallin
19 milar nature as a hard structural overlay on exoskeleton and teeth is because of convergent evolution
20                                              Exoskeletons and active prostheses promise to enhance hu
21 er, the rarity of fossilized CNSs, even when exoskeletons and appendages show high levels of integrit
22  with reductions in groups with hard exposed exoskeletons and domination by soft-bodied ascidians and
23 n nature, found in crustacean shells, insect exoskeletons and fungal cell walls.
24 s were approximately 100 times higher in the exoskeleton, and were unrelated to sampling location, st
25                  The major synthases of this exoskeleton are called penicillin-binding proteins (PBPs
26                    Carbon fibers and lobster exoskeleton as examples of biomineralized tissue have be
27  have developed a method for identifying the exoskeleton assistance that minimizes human energy cost
28 or muscle activity decreased slightly during exoskeleton-assisted walking compared to baseline, while
29                 Crustaceans shed their rigid exoskeleton at each molt yet are still capable of forcef
30 is behavior allows insects to shed their old exoskeleton at the end of every molt.
31 an be partly replaced by power input from an exoskeleton, but is it possible to reduce metabolic rate
32 dic synthesis and removal of a collagen-rich exoskeleton, but the underlying molecular mechanisms are
33 tors, including a custom-designed lower limb exoskeleton capable of delivering tactile feedback to su
34   Because of its importance to the arthropod exoskeleton, chitin biogenesis is an attractive target f
35 y their elegantly sculpted calcium carbonate exoskeletons (coccoliths), rendering them visible from s
36 owing a laboratory decision to test meat and exoskeleton combined.
37                                          The exoskeleton consumes no chemical or electrical energy an
38                              Using a robotic exoskeleton coupled with a virtual visual environment, p
39 rthropods periodically molt to replace their exoskeleton (cuticle).
40 eft circularly polarized light, possesses an exoskeleton decorated by hexagonal cells (approximately
41               We evaluated a novel pediatric exoskeleton designed to provide appropriately-timed exte
42 errestrial crabs repeatedly shed their rigid exoskeleton during moulting.
43 gels of proteins from the four layers of the exoskeleton, epidermis, limb buds and claw muscle were p
44   These findings support the use of wearable exoskeletons for the management of crouch gait and provi
45          Instead, we found evidence that the exoskeleton formation has been co-opted downstream of th
46 ution of elytra involved co-opting genes for exoskeleton formation into the wing development gene net
47                     Our understanding of the exoskeleton formation provides a unique insight into the
48           Many three-dimensionally preserved exoskeletons found from the middle Cambrian (Stage 5) Ga
49 ay, and the way in which broken parts of the exoskeleton fused during restoration seem to simulate mo
50 he uptake and distribution of Ag in over 650 exoskeletons, gills, hepatopancreas and muscles samples
51 s that function in the molting of the larval exoskeleton have been characterized previously.
52                                              Exoskeletons have evolved 18 times independently over 55
53 erall morphology confirms a role for the fly exoskeleton in determining body shape.
54 e evolution of other 'successful' phyla: the exoskeleton in ecdysozoan invertebrates and the internal
55 rganism: the skeleton in vertebrates and the exoskeleton in invertebrates.
56 signalling evolved with the emergence of the exoskeleton in the arthropods and that RR-1 containing c
57           Ecdysis (i.e., the shedding of the exoskeleton) in insects has served as a useful model for
58 re colonized by microorganisms on the insect exoskeleton, in the gut and hemocoel, and within insect
59                                   Biological exoskeletons, in particular those with unusually robust
60          These organisms build up protective exoskeletons incrementally by biologically-controlled mi
61 s in Caenorhabditis elegans suggest that the exoskeleton influences body shape in diverse organisms.
62 chitosan, a polymer isolated from crustacean exoskeletons, inhibits candidal biofilm formation in viv
63        Remodelling of the peptidoglycan (PG) exoskeleton is intimately tied to the growth and divisio
64                     Although their chitinous exoskeleton is largely resistant to chemical degradation
65 e mlt-10 gene in the hypodermis whenever the exoskeleton is remade.
66               Here we show that whenever its exoskeleton is shed, the blackback land crab Gecarcinus
67                       The evolution of their exoskeleton is well documented by fossils, but appendage
68        Production of their calcium carbonate exoskeletons is dependent not only on the environmental
69 ode of life and leathery, poorly mineralized exoskeleton makes preservation unlikely, and their fossi
70 the crystalline S-layer arrays that form the exoskeleton of many archaea and bacteria have been studi
71 zymes that cleave chitin, a component of the exoskeleton of many organisms including the house dust m
72 sive skeletogenic ability which produced the exoskeleton of more basal vertebrates.
73  in part to the fact that its members had an exoskeleton of numerous calcium carbonate valves that us
74 lating the intricate optical response of the exoskeleton of scarab beetles.
75                                          The exoskeleton of the free-living nematode, Caenorhabditis
76 years, the cell wall was considered an inert exoskeleton of the fungal cell.
77  of CCAP to inflate, pigment, and harden the exoskeleton of the next stage.
78 component of the cell walls of fungi and the exoskeletons of arthropods.
79  metabolite in this habitat is the chitinous exoskeletons of crustacean zooplankton.
80 nt, where a common nutrient is the chitinous exoskeletons of microscopic crustaceans.
81 in the environment attached to the chitinous exoskeletons of zooplankton.
82                                      Jointed exoskeletons permit rapid appendage-driven locomotion bu
83  the expected failures in wing expansion and exoskeleton pigmentation and hardening.
84                                    Cockroach exoskeletons provided biological inspiration for the man
85 y a well-organized endoskeleton to which the exoskeleton rays are connected.
86 f the epidermal layer (which synthesises new exoskeleton) remained with the shell and some remained w
87             We examined oxidative stress and exoskeleton structure, mineral content, and mechanical p
88 ndary-form infected insects retained a rigid exoskeleton structure.
89 urround themselves with a peptidoglycan (PG) exoskeleton synthesized by polysaccharide polymerases ca
90 urround themselves with a peptidoglycan (PG) exoskeleton synthesized by the penicillin-binding protei
91 nematodes and this is the only example of an exoskeleton that has been co-opted as an immune system.
92                      The shedding of the old exoskeleton that occurs in insects at the end of a molt
93 is an important constituent of the cuticular exoskeleton that plays a key role in the insect life cyc
94 ve acquired a covering, called a sacculus or exoskeleton, that made it stress-resistant.
95 legans is contained within a multifunctional exoskeleton, the cuticle, that contains a large number o
96 errestrial insects in nature, obtain a tough exoskeleton through the activity of an ancient bacterial
97 use cholera, and the arthropod intestine and exoskeleton to persist in the aquatic environment.
98 iniature medical devices to wearable robotic exoskeletons to large deployable structures for space ex
99 o create the morphology of the peptidoglycan exoskeleton together with cytoskeleton proteins that reg
100 ues in proteins incorporated into the insect exoskeleton, were characterized using electrospray ioniz
101 t in aquatic habitats (e.g., from crustacean exoskeletons), where it lives as an autochthonous microb
102            Optimized torque patterns from an exoskeleton worn on one ankle reduced metabolic energy c
103              The approach was effective with exoskeletons worn on one or both ankles, during a variet

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