ライフサイエンスコーパス: cation transport

1 and transference number t(m,+) for membrane cation transport.

2 metal recognition and discrimination during cation transport.

3 contributes to forming a pathway for organic cation transport.

4 confined spacings as nanochannels for rapid cation transport.

5 occurs as part of the catalytic cycle during cation transport.

6 e examined further for phenotype relating to cation transport.

7 lation and reordering, and thus a slowing of cation transport.

8 e 11 are responsible for altering monovalent cation transport.

9 to the membrane-embedded part that mediates cation transport.

10 led receptor pathway, membrane potential and cation transport.

11 raction with PTS rather than eserine-induced cation transport.

12 nt energy barrier, thus permitting efficient cation transport.

13 rmal surface area in RBCs and for normal RBC cation transport.

14 ittle is known about how disorder influences cation transport.

15 may be required for energy transduction and cation transport.

16 ATPase cation transporting 13A2 (ATP13A2) is an endolysosomal P

17 However, the mechanisms governing cation transport across these membranes under different

18 Significant organic cation transport activities have been found in gene fami

19 hough it has been suggested that TMEM165 has cation transport activity, direct evidence for its Ca(2+

20 Glu(206) (E206Q) resulted in loss of organic cation transport activity, whereas conserving the negati

21 alanine or tryptophan fully restored organic cation transport activity.

22 nthesis, carbohydrate uptake and metabolism, cation transport, amino acid metabolism, ubiquinone and

23 ating solution chamber, effectively blocking cation transport and eliminating conditions conducive to

24 L5 of NHE1 as important elements involved in cation transport and inhibitor sensitivity, which may in

25 t remains unclear how TRPM6 affects divalent cation transport and whether this involves functional ho

26 tive Neosepta CMS is known to block divalent cations transport and can therefore mitigate reductions

27 th faster solvent exchange leading to faster cation transport), and (3) an interfacial model wherein

28 rs implicated genes and pathways involved in cation transport, angiotensin production, and regulators

29 ring xylem refilling and for the activity of cation transport as having a significant role in the gen

30 lation and cation binding domains in various cation transport ATPase.

31 This putative cation-transporting ATPase 13A5 (Atp13a5) marker was ide

32 ATP4 is thought to be a cation-transporting ATPase responsible for maintaining l

33 ATP-binding cassette (ABC) transporter and a cation-transporting ATPase were upregulated in GECs.

34 These results suggest that PepO, a cation-transporting ATPase, and an ABC transporter are r

35 The gastric H,K-ATPase is related to other cation transport ATPases, for example, Na,K-ATPase and C

36 high degree of sequence homology with other cation transport ATPases.

37 TPase, which belongs to the P-type family of cation-transporting ATPases, is activated up to 10-fold

38 evisiae, which belongs to the P2 subgroup of cation-transporting ATPases, is encoded by the PMA1 gene

39 Within the large family of P-type cation-transporting ATPases, members differ in the numbe

40 ) RBCs demonstrate an abnormal regulation of cation transport by cell volume.

41 t 5 (M5) is thought to play a direct role in cation transport by the sarcoplasmic reticulum Ca2+-ATPa

42 Proton and sodium cation transport by these compounds has been demonstrate

43 Pump-mediated K(+)-like organic cation transport challenges the concept of rigid structu

44 ress in understanding altered red blood cell cation transport characteristics of SCD.

45 not undergo large-scale movements during the cation transport cycle.

46 hibits the Na, K-ATPase by disruption of the cation transport domain rather than the catalytic domain

47 carnitine transport function and the organic cation transport function of OCTN2.

48 mutations may not interfere with the organic cation transport function.

49 ion but significantly stimulated the organic cation transport function.

50 These couple ATP hydrolysis with cation transport, generating cation gradients across mem

51 les induce coupled chloride anion and sodium cation transport in both liposomal models and cells, and

52 ive channel regulation, leading to increased cation transport in erythroid cells.

53 r understanding of the mechanisms of organic cation transport in rat liver, little is known about the

54 n inhibitor of NKCC1, alters transepithelial cation transport in rat OMCD.

55 oposed role of this protein as a mediator of cation transport in RBC.

56 Fast cation transport in solids underpins energy storage.

57 that the filament growth can be dominated by cation transport in the dielectric film.

58 that the cAMP pathway regulates PC2-mediated cation transport in the hST.

59 for elucidation of the mechanisms of organic cation transport in the human liver and understanding of

60 tle is known about the mechanisms of organic cation transport in the human liver.

61 ransporter, which may play a role in organic cation transport in vivo.

62 SF-level gating modalities control selective cation transport in wild-type (WT) and mutant (N629D) hE

63 resulted in (i) greater pyrophosphate-driven cation transport into root vacuolar fractions, (ii) incr

64 Available data indicate that cation transport is impaired in many cells in chronic re

65 Electrogenic cation transport is known to reside in the principal cel

66 transport is Na(+)-dependent whereas organic cation transport is Na(+)-independent, we investigated t

67 PY photo-caged Zn(II) transporters, in which cation transport is triggered by photo-decaging with UV

68 wever, how the channel pore opens to mediate cation transport is unclear.

69 d human organic cation transporters, organic cation transport kinetics differed markedly.

70 cales ranging from 0.5 mus to 5 ms), (2) the cation transport mechanism is a mixture of vehicular and

71 eriments and surface analysis elucidated the cation transport mechanism, highlighting the impact of N

72 diated Fe acquisition, Fe storage, and other cation transport mechanisms.

73 ta-synthase (CBS)-pair domain divalent metal cation transport mediators (CNNMs) are an evolutionarily

74 ases and bind CBS-pair domain divalent metal cation transport mediators (CNNMs) to regulate magnesium

75 ctance is accompanied by a sharp increase in cation transport number and by pronounced open-channel l

76 utated in genes involved in gene regulation, cation transport or stress tolerance were shown to be hi

77 ode a protein of 732 amino acids, similar to cation transport P-type ATPases in the Cpx-type family.

78 the Saccharomyces cerevisiae Atx1 is Ccc2, a cation transporting P-type ATPase located in secretory v

79 ne encodes a highly homologous member of the cation-transport P-type ATPase family.

80 st Ccc2 protein, which are integral membrane cation-transporting P-type ATPases involved in copper tr

81 ses resembles that of the well-characterized cation-transporting P-type ATPases, and it is unknown wh

82 rotein (WNDP) belongs to the large family of cation-transporting P-type ATPases, however, the detaile

83 le proposed for the more extensively studied cation-transporting P-type ATPases.

84 endocytic compartments, but their kinship to cation-transporting P-type transporters raised doubts ab

85 s 5 and 8 of the P-ATPases contribute to the cation transport pathway and that the fundamental mechan

86 t the absorption of light by an electron and cation-transporting polymer film reversibly modulates it

87 bule has 2 main secretory cell types: active cation-transporting principal cells, wherein the aquagly

88 A carrier-mediated organic cation transport process appears to exist in the conjunc

89 ine, but not by substrates for other organic cation transport processes identified in blLPM vesicles,

90 bbit (rb) exhibit differences in citrate and cation transport properties.

91 d the phylogenetic relationships of over 150 cation transport proteins.

92 extramembraneous ATP binding domain and the cation transport regions of the Na,K-ATPase.

93 analysis predicted that the hub gene CHAC1 (cation transport regulator homolog 1) was regulated by t

94 that an Arabidopsis thaliana protein with a cation transport regulator-like domain, hereafter referr

95 CHAC1 (cation transport regulator-like protein 1), a novel gene

96 Our work sheds light on the design of cation transport requirements for high-energy reversible

97 eexisting networks designed for adhesion and cation transport/response and that its regulation occurs

98 The cation transport selectivities of the Ca2+ ionophores A2

99 of artificial channels presenting proton vs cation transport selectivity performances.

100 Furthermore, the structure reveals that cation transport site II is occupied by Mg(2+), and crys

101 hrough conformational changes induced at the cation transport site located within the membrane or at

102 the carnitine transport site and the organic cation transport site were not identical.

103 n the cardiac glycoside binding site and the cation transport sites of the Na,K-ATPase transpires giv

104 ubnetwork was enriched for genes involved in cation transport, synaptic transmission, and transmissio

105 or the components of an ATP-binding cassette cation-transport system (troABCD) and a DtxR-like transc

106 W solution as assessed by tetraethylammonium cation transport (TEA).

107 n pairing generally has an adverse effect on cation transport, thereby slowing down charge transport.

108 with the previously known role of SLC11A1 in cation transport, these effects were enhanced by elevati

109 nt adsorption and hydrodynamic dispersion on cation transport through a reactive porous medium with a

110 x 10(-14) cm(2)/s for ambipolar electron and cation transport throughout the film.

111 n gerO spores but not the ability to restore cation transport to E. coli cells defective in K(+) upta

112 The electrodriven cation transport together with the use of highly Cs+ sel

113 ing the ED stack design to restrict divalent cation transport toward the cathode.

114 In peripheral tissues, organic cation transport via some OCTs is inhibited by corticost

115 Plots of the log of the rate of cation transport vs the log of the ionophore concentrati

116 Long-distance radical cation transport was studied in DNA condensates.

117 d without external Na(+) and K(+) represents cation transport when normal occlusion at sites I and II

118 compared with SGLT1 and the sugar-activated cation transport without sugar transport that occurs in