ライフサイエンスコーパス: curling

1 ntrast to wild-type plants that exhibit root curling.

2 ubulin-associated GTP promotes protofilament curling.

3 is elegans, egg laying and male ventral tail curling.

4 ntial cell elongation responses such as root curling.

5 w to copulate because of maladroit abdominal curling.

6 th a marked decrease in root hair growth and curling.

7 uxin deficient mutant cytokinin induced root curling 2 (ckrc2) in this work reveal that CKRC2 encodes

8 ; P=0.042), prevalence of posterior systolic curling (34 [94%] versus 3 [19%]; P<0.001), and basal to

9 The procedure of curling a ribbon by running it over a sharp blade is com

10 of the leaflets caused by posterior systolic curling accounts for a mechanical stretch of the inferob

11 s had early-onset parkinsonism (dystonic toe curling, action tremor, masked face, bradykinesia, stoop

12 The model identifies factors that optimize curling and clarifies the physical mechanisms underlying

13 ited severe compound leaf defects, including curling and deep serration of leaf margins, shortened pe

14 males also produces defects in ventral tail curling and enhances the turning defects in ser-1 mutant

15 ngs exhibit altered responses to NPA in root curling and hypocotyl elongation.

16 These phenotypes include leaf curling and the partial conversion of later-arising caul

17 ferential topology recapitulate the observed curling and thickening, in support of an 'inside-to-outs

18 Medium with 2 mM ATP induces root curling, and 3 mM ATP stimulates lateral root growth.

19 ion and morphological damage (fragmentation, curling, and aggregation).

20 al abnormalities that include stunting, leaf curling, and the loss of apical dominance.

21 a His tag being approximately 65 A long and curling around the base of the structure.

22 odes placed within prey items show that this curling behavior at least doubles the field strength wit

23 6 unit cells there is a complex flux-closure curling behaviour resembling an incommensurate phase.

24 he Mtnin mutants undergo excessive root hair curling but are impaired in infection and fail to form n

25 itiate 10 to 20 h after the completion of RH curling, by which time major modifications have occurred

26 rates into the interlayers of h-BN along the curling edge, followed by an immediate drastic gasificat

27 tin pentamer, inactive in inducing root hair curling (HAD) or cortical cell division (NOI) in G. soja

28 n uterine muscles, and the reduced abdominal curling in males correlates with alteration in motor neu

29 racterizations of a phot1-5 rcn1-1 (for root curling in n-naphthylphthalamic acid1) double mutant, in

30 played a similar ability to induce root hair curling in response to rhizobia or Nod lipochitooligosac

31 e and a passive layer show rapid, reversible curling in response to stimulus DNA strands added to sol

32 er, it was observed that the absence of root curling in response to touch can be reverted by jasmonic

33 to chemicals used in hair straightening and curling increased the odds that the infant was preterm o

34 ence of association between brain tumors and curling iron, heating pad, vibrating massager, electric

35 Leaf curling is suppressed by sep3 and ft mutations and enhan

36 of axr1, namely, short petioles, downwardly curling leaves, short inflorescence, and reduced fertili

37 A spin vortex consists of an in-plane curling magnetization and a small core region (~10 nm) w

38 ic topological structures characterized by a curling magnetization around a highly stable nanometric

39 terized as a negative regulator of rice root curling mediated by jasmonic acid.

40 is ruled by the geometrical conformations of curling MT-protofilaments entangled in kinetochore fibri

41 The curling of a graphitic sheet to form carbon nanotubes pr

42 r) sides of lateral organs results in upward curling of leaf blades.

43 red growth, leaf chlorosis, and necrosis and curling of leaf margins.

44 the tips of microtubules, tea1p prevents the curling of microtubules around the cell ends, whereas it

45 ss of EIR1/AGR1/PIN2 function abolishes root curling of mlo4, mlo11, and wild-type seedlings.

46 agl24 svp mutations, the plants show upward curling of rosette and cauline leaves, in addition to ea

47 rature variation initiates the expansion and curling of the bulk h-BN.

48 al part of the neural tube, which forms by a curling of the neural plate.

49 ability of the NodC- mutant to induce marked curlings or infection threads within root hairs.

50 d with a higher expression rice ROOT MEANDER CURLING (OsRMC), which encodes a receptor-like kinase ch

51 ends with the ruptured erythrocyte membrane curling outwards, buckling, everting and vesiculating.

52 esults demonstrate that the exaggerated root curling phenotypes of the mlo4 and mlo11 mutants depend

53 tronic devices, it is wise to investigate if curling polarization structures are innate to ferroelect

54 Protofilament curling presumably drives the transition from tip struct

55 ly demonstrate the spring-like elasticity of curling protofilaments.

56 found between mitral annulus disjunction and curling (R=0.85).

57 hylphthalamic acid on the inhibition of root curling, raising the possibility that transport of auxin

58 ype seedlings mimics the rcn1 defect in root curling, root waving and hypocotyl hook formation assays

59 nsertion mutation at this locus impairs root curling, seedling organ elongation and apical hypocotyl

60 nvolves the union in space of two edges of a curling sheet and results in a substantial number of unc

61 ll as shoot phenotypes including upward leaf curling, shortened siliques and narrow lateral branch an

62 moters, derived from the Cestrum yellow leaf curling virus, drives levels of constitutive transgene e

63 initiating pore opening and outward membrane curling, we develop a model of the dynamics of the red b