ライフサイエンスコーパス: costal

1 ommunity detection using Leiden's algorithm (CosTaL).

2 constitutive low signaling by titrating out Costal.

3 ndent vasodilatation was 21% lower in medial costal 1A arterioles from O rats (p < 0.001).

4 reased ACh-mediated vasodilatation of medial costal 1A arterioles from Y and O rats but did not elimi

5 The Drosophila kinesin-family protein Costal 2 (Cos2) and its mammalian ortholog Kif7 play dua

6 uding the role of the kinesin-family protein Costal 2 (Cos2), which directs Ci processing in Drosophi

7 We also found that the Ci binding partner, Costal 2 (Cos2), which silences Ci in the absence of Hh,

8 with or without the kinesin-related protein Costal 2 (Cos2).

9 -threonine kinase Fused (Fu) and the kinesin Costal 2 (Cos2, also known as Cos), yet Fu does not have

10 Fused (Fu), Suppressor of fused (Sufu), and Costal-2 (Cos2) or the vertebrate homologs Kif27/Kif7.

11 plex containing Ci, the kinesin-like protein Costal-2 (Cos2), the serine-threonine kinase Fused (Fu),

12 lded and stabilized by the atypical kinesin, Costal-2 (Cos2).

13 Further our data show that loss of PKA or Costal-2 activity does not fully mimic Hh signaling, dem

14 erary border cells, was found to disrupt the costal-2 locus, indicating a role for Hedgehog signaling

15 es now show that the kinesin-related protein Costal-2 provides a physical link between the transmembr

16 ontaining Ci and the kinesin-related protein Costal-2 to bind microtubules.

17 find Sex-lethal in a complex with Fused and Costal-2, both downstream components of the pathway.

18 mponents, including the kinesin-like protein Costal-2, the serine-threonine kinase Fused, and Suppres

19 )), and with the microtubule-binding protein Costal-2.

20 patterns of response were identical for the costal and crural diaphragms.

21 rating Smoothened cytoplasmic tails activate Costal and Fused, driving the regulatory complex to its

22 Recently, Costales and colleagues (J.

23 be found in other tetrapods that breathe by costal aspiration and locomote with a lateral undulatory

24 have been an exaptation for the evolution of costal aspiration breathing in stem amniotes.

25 Specifically, CosTaL builds an exact kNN graph using cosine similarity

26 Purpose To assess the incidence of costal cartilage (CC) fractures in whole-body computed t

27 oups: control (n = 5), irradiated homologous costal cartilage (IHCC, n = 10), and expanded polytetraf

28 29), prominent convexity of anterior rib or costal cartilage (n = 19), prominent asymmetric costal c

29 tal cartilage (n = 19), prominent asymmetric costal cartilage (n = 20), well-defined paracostal subcu

30 Purpose To evaluate whether adding costal cartilage calcification (CCC) to coronary artery

31 ficant age-related elastic behavior of human costal cartilage could be shown with the unconfined comp

32 n addition, embryos with paternal UPD12 have costal cartilage defects and hypo-ossification of mesode

33 imal aesthetic outcomes and morbidity at the costal cartilage donor site.

34 d rhinoplasty, nasal vestibular stenosis, or costal cartilage grafts or if the second surgery did not

35 r cartilage, the biomechanical properties of costal cartilage have not yet been extensively explored.

36 all (< 1-cm) subcutaneous nodule adjacent to costal cartilage in five.

37 tilted" sternum in six; prominent asymmetric costal cartilage in four; bifid rib in one; and well-def

38 Extensive subperiosteal costal cartilage resection and perichondrial sheath deta

39 me the anisotropic elastic behavior of human costal cartilage.

40 After exposing the deformed costal cartilages, a short chip was resected medially ad

41 Costal chondrocyte and mixture constructs were morpholog

42 Costal chondrocyte constructs produced almost 40 times m

43 between human NK cells and isolated porcine costal chondrocytes (PCC).

44 uman articular chondrocytes and immortalized costal chondrocytes (TC28 cells).

45 ondrocytes and immortalized NTPPPH-deficient costal chondrocytes (TC28 cells).

46 e found that wild-type Col11a1 expression in costal chondrocytes suppresses expression of Pax1 and of

47 This study demonstrates the ability of costal chondrocytes to produce extracellular matrix that

48 rtilage derived from highly passaged minipig costal chondrocytes, a species relevant to the preclinic

49 linically relevant cell sources by comparing costal chondrocytes, dermal fibroblasts, a mixture of th

50 e articular chondrocytes to expanded minipig costal chondrocytes, yielding a 46% improvement in aggre

51 ects in collagen matrix protein secretion by costal chondrocytes.

52 consist of highly disorganised vertebrae and costal defects, are similar to those associated with the

53 ol I, fifteen normal subjects maintained the costal diaphragm at inferior/superior positions by full

54 fiber type proportions and FEV1, we obtained costal diaphragm biopsies on 40 subjects whose FEV1 rang

55 Costal diaphragm biopsies were taken from five patients

56 The number of medial costal diaphragm FAs was lower in old rats.

57 d (O) Fischer-344 rats, the number of medial costal diaphragm FAs was quantified.

58 n microvascular PO2 (PO2m) within the medial costal diaphragm of control (C, n = 10) and emphysematou

59 In the medial costal diaphragm vasculature, ageing is associated with

60 We hypothesized that, in the medial costal diaphragm with old age, there would be fewer feed

61 c and sternohyoid muscles, as well as in the costal diaphragm.

62 of first-order (1A) arterioles in the medial costal diaphragm.

63 Costal diaphragmatic biopsy samples were obtained from 7

64 We obtained biopsy specimens from the costal diaphragms of 14 brain-dead organ donors before o

65 The average number of medial costal FAs was lower in the rat diaphragm with old age (

66 We demonstrate that CosTaL generally achieves equivalent or higher effective

67 ndicated by the combined evaluation metrics, Costal has high efficiency with small datasets and accep

68 odel where low signaling is initiated when a Costal inhibitory site on the Smoothened cytoplasmic tai

69 dition, alterations in transverse processes, costal joints, and zygapophyses were detected.

70 esence of splenomegaly > or = 5 cm below the costal margin (BCM) or thrombocytosis > or = 700 x 10(9)

71 plenomegaly greater than 5 cm below the left costal margin or splenomegaly-related symptoms should re

72 s underestimated the distance from the right costal margin to the liver edge by only about 2.4 centim

73 alpable splenomegaly (>/=5 cm below the left costal margin), Eastern Cooperative Oncology Group perfo

74 on the midway of the xiphoid process and the costal margin, and 1 cm above the umbilicus, respectivel

75 icularly when exceeding 15 cm below the left costal margin, or with splenomegaly-related symptoms, co

76 f the ribs into the turtle shell negates the costal movements that effect lung ventilation in other a

77 Depiction of the undersurface of the long costal muscle slips of the diaphragm on supine plain rad

78 On the CT scans, the costal muscle slips were clearly defined as bands or sma

79 SmoC mimics costal mutants.

80 (smooth or nonsmooth), and attachment to the costal pleura (broad or narrow) were documented.

81 f solid noncalcified nodules attached to the costal pleura (CP-NCNs) at baseline low-dose CT and to i

82 the lungs, only lesions in contact with the costal pleura are accessible to ultrasound-guided interv

83 e noncalcified solid nodules attached to the costal pleura less than 10.0 mm in average diameter with

84 Muscle slips of the costal portion of the diaphragm were depicted in the rig

85 muscle were obtained from the anterolateral costal regions of the stimulated and inactive hemidiaphr

86 f both cv HI10 and cv Spence contained dense costal ridges of papillae.

87 ce a regulatory complex that includes Fused, Costal, Suppressor of Fused and Cubitus interruptus.

88 As a graph-based clustering method, CosTaL transforms the cells with high-dimensional featur

89 bears long, cranially and ventrally oriented costal (transverse) processes, implying powerful trunk m

90 ride length [10], and they inhibit effective costal ventilation [9, 11].