ライフサイエンスコーパス: body length

1 e.g., decreasing sensitivity with increasing body length).

2 which plays a key role in the development of body length.

3 which prey typically moved approximately one body length.

4 uction of body weight as well as a decreased body length.

5 f long-horned bees bear antennae that exceed body length.

6 l skeleton, kinked pectoral fins and a short body length.

7 itoid) of length to diameter with increasing body length.

8 ecies, achieving projection distances of 2.5 body lengths.

9 romone trails that can be followed over many body lengths.

10 ballistically project their tongue up to two body lengths, achieving power outputs nearly three times

11 testine-specific sma-5(RNAi) Besides reduced body length, an increased time of development, reduced b

12 generation of fish with dramatically reduced body length and a short, curly tail.

13 )/Vc ratio remained constant with increasing body length and did not differ for infants with BPD and

14 uble heterozygotes demonstrate the increased body length and head size.

15 otypic variability in developmental rate but body length and mass at hatching were largely insensitiv

16 fferent C. elegans developmental phenotypes, body length and sex ratio, as examples, we showed that t

17 Fetal head circumference and body length and weight were estimated by repeated ultras

18 ition, synergistic effects were observed for body length and weight, suggesting possible compensatory

19 8.2% and captured variation in ramus height, body length, and anterior cranial base orientation.

20 tion of fat and lean mass, food consumption, body length, and blood levels of cholesterol and nonfast

21 FT subjects after adjustment for race, sex, body length, and corrected age.

22 owever, growth as determined by body weight, body length, and femoral length did not differ from wild

23 ing to a smaller head circumference, shorter body length, and lower body weight at birth (all P < 0.0

24 l vault length, maxillary length, mandibular body length, and mandibular shape index.

25 accompanied by reduced body mass, shortened body length, and reduced bone mineral density (BMD) and

26 They were significantly shorter in overall body length as well as in the femur and tibia lengths.

27 of the turn, the parasite moves forward one body length at a rate of approximately 1-3 microm/s.

28 Body length at settlement, but not condition, affected g

29 Biweekly body weight (BW), body length (BL), waist circumstance (WC), and body mass

30 d (FG) was applied to the spinal cord at 40% body length (BL; measured from anterior to posterior fro

31 ns) were performed in the spinal cord at 30% body length (BL; normalized distance from the head) or 5

32 Body length, BMC and BMD, but not body mass, are rescued

33 Phenotypic data on individual adult body length, body depth, stream entry timing and reprodu

34 Possible associations of age, body length, body weight, body surface area, and heart r

35 rats, STZ rats had reduced body weight, and body length, but minimally affected corneal size.

36 mage analysis protocols are used to quantify body length, circulation, heart rate, pericardial area (

37 Body length decreased sharply during the first 6 to 12 m

38 Increase in both maximum and minimum body length early in plesiosaurian history suggests a dr

39 ted for filter-feeding with an unprecedented body length exceeding 2 m, indicating a new direction in

40 fter 7 weeks, developed reduced body weight, body length, fat mass, lean mass, and leptin levels.

41 al capacity (FVC) was highly correlated with body length; however, after accounting for length, age w

42 D(M) and Vc increased with increasing body length; however, infants with BPD had significantly

43 s a BMP-like signaling pathway that controls body length in C. elegans lon-2 acts genetically upstrea

44 of bone morphogenetic protein (BMP)-mediated body length in C. elegans.

45 lines, accompanied with a small reduction in body length in the Negr1-I87N mutants.

46 ial mates are often separated by hundreds of body lengths in a 3D environment.

47 The slope of FRC (in milliliters) versus body length (in centimeters) for all 23 recipients studi

48 he relationship between aphid and parasitoid body length is substantially increased, if the average l

49 ogenous mechanism that determines vertebrate body length is unknown but must involve loss of chordo-n

50 of M (i.e., G proportional to M(3/4)); plant body length L (i.e., cell length or plant height) scales

51 ruct tunnels with diameter, D, comparable to body length, L = 3.5 +/- 0.5 mm.

52 chromosome 2 occurred in the same region as body length, lean tissue mass, and bone mineral content

53 analyzes hundreds of individual animals for body length, locomotion speed, and lifespan.

54 After adjustment for body length, males had greater Crs values than did femal

55 In rare cases, changes of body length may occur in response to harsh environmental

56 und in children with FA, including shortened body length, microcephaly, and microophthalmia, which ar

57 directional locomotion (310 microm/s or 1.3 body lengths/min) and 2D rotational steering (2 degrees

58 ator is estimated to have grown to a maximum body length of at least 11 to 12 meters and body weight

59 from an Early Cambrian arthropod that had a body length of several centimetres.

60 Total body length of the species is estimated to have reached

61 zooplankton biomass inferred by density and body length of zooplankton.

62 aphids and 37 species of their parasitoids), body lengths of 2,151 parasitoid individuals were, to an

63 Capinatator praetermissus reached body lengths of nearly 10 cm exclusive of fins, a much l

64 o an excellent approximation, related to the body lengths of their individual aphid hosts by a power

65 ture, watershed area, resident fish species, body length, or lipid content.

66 Accordingly, body weight, body length, organ weight, and bone mass acquisition wer

67 ionship is maintained between fin length and body length over the lifespan of the growing fish.

68 e 3 mo predicted greater subsequent gains in body length (P < 0.001 and P = 0.007 in formula milk-fed

69 Crs and V30E increased with increasing body length (p < 0.001).

70 proximately 156 mum s(-1), which is over 1.5 body lengths per min.

71 irection of the Pt end at speeds of up to 10 body lengths per second.

72 etween masseter muscle weight and mandibular body length (r = 0.68; p < 0.01), cranial vault length (

73 AT correlated positively with age (r=0.848), body length (r=0.871), body surface area (r=0.856), and

74 engraftment had a median 7.5-cm increase in body length (range, 6.5-8.0 cm) 6 months after transplan

75 ar mislocalization of birefringent material, body-length retraction, and NaCl sensitivity, phenotypes

76 self-propelled at a very high speed (of ~20 body lengths s(-1)) in a 0.001% hydrazine solution due t

77 propelled at an ultrafast speed (of over 350 body lengths s(-1)), and can operate in very low levels

78 est 2 orders of magnitude smaller than the 2 body lengths/s (approximately 60 cm/s) for motion on har

79 play an ultrafast propulsion (as high as 100 body lengths/s) along with attractive capabilities inclu

80 Regression equations, based on scutal index (body length/scutal width), were developed to determine t

81 ants show a strongly increased head size and body length, suggesting a greater contribution from fam5

82 posterior lateral line system and decreased body length, suggesting that RL-TGR is involved in depos

83 pulations had larger heads relative to their body length than mainland populations; larger heads are

84 When the toads hopped a distance of two body lengths, the proximal and central segments strained

85 n diameters do not increase in proportion to body length, then absolute and relative conduction delay

86 allions and over one-hundred times a mouse's body length, there are few functions known aside from sp

87 Overall, there was no improvement in body length, tibial length, and growth plate width at th

88 Body length, tibial length, and growth plate width did n

89 Tick engorgement index (TEI), ratio of body length to scutal width, was identified to be the on

90 The model also indicates that the number of body lengths travelled by walking and swimming migrants