ライフサイエンスコーパス: curly

1 olymerized on lipid membranes decorated with curly.

2 ransformations, from normal to semicoiled to curly 1 and then, when the motor again spun CCW, back to

3 to occur in the sequence normal, semicoiled, curly 1, with changes in the direction of movement of th

4 Here, we show that 'curly', a region from the IQGAP family of proteins from

5 tributing to the formation of heterogeneous, curly, and tangled fibrils.

6 The "curly arrow" of Robinson and Ingold is the primary tool

7 heory." In contrast with counting rules and "curly-arrow" descriptions of destructive QI, magic numbe

8 Our results clarify that curly arrows are rooted in physical reality-a notion whi

9 rt that the bond rearrangements expressed by curly arrows can be directly observed in ab initio compu

10 The new mutation, curly bare (cub), was mapped to distal Chr 11 and the mo

11 es of morphology: monopolar, simple bipolar, curly bipolar and radial shaped; they were localized in

12 The curly bipolar cells had a higher membrane conductance, h

13 urons (monopolar, radial, simple bipolar and curly bipolar) were identified.

14 quations (2) and (4) erroneously displayed a curly bracket on the right hand side of the equation.

15 oiety containing a {Se(V)-Se(V)} bond (where curly brackets indicate a moiety, not a molecule) and re

16 lis and results in the formation of aberrant curly cells.

17 of the dominant Mcub allele confers a full, curly coat in cub/cub mice.

18 association studies for milk production and curly coat, using imputed sequence variants, and identif

19 lotype spanning ~600 Kb was found in all the curly coated cats.

20 trol association study was conducted using 9 curly coated Selkirk Rex and 29 controls, including stra

21 well as a coding SNP that is associated with curly-coated dogs.

22 could form open-coiled, straight, normal, or curly conformations.

23 In the present study, curly endive (Cichorium endivia L. var. crispum) and esc

24 were significantly affected by variety, with curly endive showing on average higher scores in compari

25 ominated by a straight body segment but with curly entangled top, we have created gecko-foot-mimetic

26 d at lower concentrations, whereas short and curly fibrils containing a mixture of alpha-helical and

27 The formation of short and curly fibrils is preceded by the formation of a small nu

28 conditions, the oligomers convert into thin, curly fibrils that interact with thioflavin-T, suggestin

29 The zebrafish curly fry (cfy) mutation leads to embryonic lethality an

30 ment, and differentiation, between Caucasian curly hair and naturally straight hair was performed.

31 lude taurodontism, enamel hypoplasia, kinky, curly hair at birth and increased thickness and density

32 he principal clinical features include kinky/curly hair in infancy, enamel hypoplasia, taurodontism,

33 features with Lrrc8a(-/-) mice that include curly hair, infertility, reduced longevity, and kidney a

34 hair xenografts obtained from straight- and curly-haired individuals was found to result in the decr

35 muscle myosin II filaments and expression of curly in mammalian cells leads to highly curved actin st

36 Strikingly, curly induced actin filament rings contract upon the add

37 nrichment with frozen (13%) and freeze-dried curly kale (3%), the naturally cloudy apple juice was ch

38 vegetable, spinach, broccoli, savoy cabbage, curly kale and green pepper, by measuring the ferritin r

39 Curly kale is a robust, cold tolerant plant with a high

40 ice with addition of frozen and freeze-dried curly kale leaves.

41 t activity of beverages with the addition of curly kale ranged from 6.6 to 9.4mumol Trolox/mL.

42 A combination of eol1 with the curly leaf (clf) allele, carrying a mutation in the cata

43 onents of polycomb-group proteins, including CURLY LEAF (CLF) and LIKE HETERCHROMATIN PROTEIN 1 (LHP1

44 , the repressive histone methyl transferases CURLY LEAF (CLF) and SWINGER (SWN), and the gene silenci

45 The plant Polycomb-group (Pc-G) protein CURLY LEAF (CLF) is required to repress targets such as

46 come by partial loss of polycomb activity in curly leaf (clf) mutants, implicating the SWI2/SNF2 chro

47 CURLY LEAF (CLF), an Arabidopsis homolog of enhancer of

48 llele of the Enhancer of Zeste E(z) ortholog CURLY LEAF (CLF), clf-59.

49 at of severe mutations in another Pc-G gene, CURLY LEAF (CLF), suggesting that the two genes may act

50 gated the molecular mechanism underlying the curly leaf and early flowering phenotypes caused by redu

51 It is shown here that the CURLY LEAF gene of Arabidopsis is necessary for stable r

52 d by the suppression of petal defects of the curly leaf mutant by the pie1 mutation.

53 but defines a locus distinct from phyB, clf (curly leaf), and elf3 (early-flowering 3).

54 redundantly by the E(z) homologs SWINGER and CURLY LEAF.

55 t counteracts the PcG-repressive activity of CURLY LEAF.

56 oss in MIPS1 resulted in smaller plants with curly leaves and spontaneous production of lesions.

57 der plants of the over-expressing lines have curly leaves and were generally smaller in stature.

58 notypes including long and bending petioles, curly leaves, accelerated senescence, and constitutive e

59 s due to the shear-induced alignments of the curly segments of the nanotubes.

60 placed with those of closely related tobacco curly shoot virus (isolate Y35).

61 ed, both ssDNA and dsDNA, regions of tobacco curly shoot virus (TCSV) and hepatitis B virus (HepBV) g

62 The two mutant strains examined, curly tail (ct) and splotch-delayed (Pax3Sp-d), develop

63 Conversely, loss of Irf6 function caused a curly tail and coincided with a reduction of Tfap2a and

64 scued morphological abnormalities, including curly tail and cyst formation in the pronephric kidney,

65 recently identified as a candidate gene for curly tail based on chromosomal location and the occurre

66 PKC expression and applied PKC inhibitors to curly tail embryos developing in culture.

67 Under normal maternal dietary conditions, curly tail embryos that developed cranial NTDs had signi

68 is known to lead directly to spina bifida in curly tail embryos.

69 ave previously been found to prevent NTDs in curly tail embryos.

70 rmate has also been found to prevent NTDs in curly tail embryos.

71 ed in the spinal region of neurulation-stage curly tail embryos.

72 revention, we examined cell proliferation in curly tail embryos.

73 the known cellular defect leading to NTDs in curly tail is unknown.

74 sion of Grhl3, we generated Grhl3-expressing curly tail mice by bacterial artificial chromosome-media

75 Curly tail mice do not carry a coding region mutation in

76 to test the hypothesis that spina bifida in curly tail mice results from insufficient expression of

77 tly reducing the incidence of spinal NTDs in curly tail mice, a genetic model of folate-resistant NTD

78 ake on embryonic MI status and metabolism in curly tail mice, which are genetically predisposed to NT

79 ogenesis and etiology of spina bifida in the curly tail mouse closely resemble defects in humans, pro

80 hl3 expression in causing spinal NTDs in the curly tail mouse model.

81 In curly tail mutant mice, there can be a failure of the ne

82 The curly tail mutant mouse provides a model of folate-resis

83 However, the causative curly tail mutation has not been established, while the

84 Z construct is sufficient to rescue both the curly tail phenotype and the skeletal defects observed i

85 Mutant mice display a curly tail phenotype consistent with Zic2 loss-of-functi

86 neralization and reduces the severity of the curly tail phenotype.

87 fest severe bone calcification defects and a curly tail phenotype.

88 Spina bifida in curly tail results from a cell type-specific proliferati

89 s characteristic of defective cilia, such as curly tail up, edema, and abnormal pronephric kidney dev

90 nd is also characterized by transient edema, curly tail, generalized organ hypoplasia, including the

91 ding neural tube defects, a shortened and/or curly tail, no genital tubercle, blind-ended colons, hyd

92 ramatically reduced body length and a short, curly tail.

93 f the pathogenic sequence leading to NTDs in curly tail.

94 klc2 in Danio rerio revealed mild to severe curly-tail phenotype, which is suggestive of a neuromusc

95 s sagrei, and one of its main predators, the curly-tailed lizard Leiocephalus carinatus.

96 We show that curly-tailed lizards destabilized the coexistence of com

97 resence/absence of predatory ground-dwelling curly-tailed lizards in a replicated set of island ecosy

98 eover, whereas adding either green anoles or curly-tailed lizards lengthened food chains on the islan

99 nolis smaragdinus) and/or new top predators (curly-tailed lizards, Leiocephalus carinatus).

100 d develop a symptomless infection and severe curly top symptoms, respectively.

101 tious clones corresponding to CaLCuV or Beet curly top virus (BCTV), which are classified in differen

102 viruliferous and viruliferous [carrying beet curly top virus (BCTV)] beet leafhoppers [Circulifer ten

103 determine if the related L2 protein of Beet curly top virus (BCTV, genus Curtovirus) also has suppre

104 ng the replication origin of the Beet severe curly top virus (BSCTV), a model DNA virus, was created.

105 The related L2 protein of Beet curly top virus (genus Curtovirus) lacks transcription a

106 The related L2 protein of Beet curly top virus (genus Curtovirus) shares the pathogenic

107 Finally, we demonstrate that Beet curly top virus L2- mutant DNA present in tissues that h

108 syringae pv tomato DC3000 bacterium and Beet curly top virus.

109 s, which is consistent with the feature of a curly type, regardless of motor switching; the flagella

110 The zebrafish mutation curly up (cup) affects the zebrafish ortholog of polycys

111 ture formation in polycystin 2 morphants and curly up polycystin 2 mutants.

112 nt monomers in properdin oligomers conform a curly vertex that holds together the AP convertase, inte

113 ltaCR1, display a phenotype characterized by curly vibrissae and wavy hair.

114 eyelids open and demonstrate a wavy coat and curly vibrissae.

115 ld be easily identified by the phenotypes of curly whiskers and wavy, sheen pelage hair.

116 e are viable and fertile but have wavy hair, curly whiskers, and abnormal hair follicle shape and arr

117 These mice have a mild phenotype (wavy coat, curly whiskers, and runted stature) and normally develop

118 n a phenotype characterized by wavy hair and curly whiskers, and was associated with increased EGFR a

119 s, such as delayed growth, a waved coat, and curly whiskers, correlated with decreased transforming g

120 o a phenotype characterized by wavy hair and curly whiskers.

121 e Trpv3 gene also exhibit wavy hair coat and curly whiskers.

122 Surprisingly, curly-wing co-occurs with similarly protective silent "f

123 crosses and genomic and mRNA sequencing that curly-wing expression is associated with variation on a

124 Curly-wing inhibits males' ability to sing, protecting t

125 nted the emergence of an adaptive phenotype "curly-wing" in Hawaiian populations of field crickets (T

126 nown to accompany flatwing, and we find that curly-wing, too, negatively impacts male courtship abili

127 sistence length of ~10 um, binding of mobile curly within lipid membranes generates actin filament ar