ライフサイエンスコーパス: co-transport

1 els (138 A long) to allow for intermolecular CO transport.

2 , Thr(39), and Met(46) participate in sodium co-transport.

3 ng site that is essential in the coupling of co-transport.

4 ng a functional role during sodium/bile acid co-transport.

5 xchanger and that protons are unlikely to be co-transported.

6 Because NKCC1 co-transports 1 Na(+), 1 K(+) and 2 Cl(-), it is electro

7 Na:2Cl:K co-transport activity was assessed as the initial rate o

8 of Ang II and the inhibitory effect of NO on co-transport activity, and, furthermore, Ang II failed t

9 led by the action of Muller-cell Na(+)-HCO3- co-transport and carbonic anhydrase.

10 dicate that MD-NO directly inhibits Na:2Cl:K co-transport and that NO and Ang II independently alter

11 re complex mechanisms involve having the two co-transported and then opsin finds its way into the pla

12 during hyperosmotic stress and functions by co-transporting betaine and Na(+) into bacterial cells.

13 ighly cooperative and suggests that CmpA may co-transport bicarbonate and calcium or that calcium act

14 Proton and SO(4)(2-) are co-transported by AtSULTR4;1 and a proton gradient signi

15 anic anions (e.g. leukotriene C(4)) and also co-transports certain unmodified xenobiotics (e.g. vincr

16 ssible mechanism for lactose/proton symport (co-transport) consistent with both the structure and a l

17 cipient food webs(1,2) that may be offset by co-transported contaminants(3,4).

18 -dependent equations of heat conductance and CO transport, coupled with respective photo-chemical pro

19 This gene encodes the ZIP8 protein which co-transports divalent metal cations, including heavy me

20 ture, intermediates involved in lactose/H(+) co-transport have been suggested.

21 neurons, AdV induced CAR internalization and co-transport in axons, suggesting that CAR was linked to

22 pathway mediates sodium-dependent phosphate co-transport in LLC-PK1 cells.

23 lomerular feedback (TGF) depends on Na-K-2Cl co-transport in the macula densa (MD), but it is less cl

24 anger NHE3 and is increased by Na(+)-glucose co-transport in vitro, but the mechanisms of this up-reg

25 cids from the distal ileum via active sodium co-transport, in a multistep process, orchestrated by ke

26 In villus cells, Na-glutamine co-transport inhibition observed during inflammation was

27 ing precise binding sites for substrates and co-transported ions and changes in the tertiary structur

28 , and show the transporter's engagement with co-transported ions and the binding mode of inhibitors.

29 ded state of the transporter upon binding to co-transported ions was formed and LPS-Lips triggered th

30 ne, brush border membrane (BBM) Na-glutamine co-transport is inhibited in villus cells (mediated by B

31 Physiologically, FNT-mediated proton co-transport is vital when monocarboxylic acid products

32 of GlcP(Se) and crucial for the glucose/H(+) co-transport mechanism.

33 mpartment into the extracellular medium by a co-transport mechanism; and (c) disruption of the gene e

34 cted for the electrogenic inward movement of co-transported Na(+) In contrast, glutamate application

35 ctions as a Na(+) sensor, binding one of two co-transported Na(+) ions, (ii) Asp-124 interacts with 7

36 he uptake of anionic substrates to typically co-transported Na(+).

37 In Xenopus oocytes, HvHKT2;1 co-transports Na+ and K+ over a large range of concentra

38 roteins, Na+-H+ exchange (NHE) and Na+-HCO3- co-transport (NBC) in guinea-pig isolated ventricular my

39 Na(+)/H(+) exchange (NHE1) and Na(+)-HCO3(-) co-transport (NBC) is essential for maintaining a low cy

40 s grown either in the presence or absence of CO transported Ni(2+) with a K(m) of 19 +/- 4 microM and

41 Activity of Na+-K+-2Cl- co-transport (NKCC1) in epithelia is thought to be highl

42 Capillary osmotic (CO) transport of electrolytic liquids driven by a concen

43 We here demonstrate axonal co-transport of BRP and RBP using intravital live imagin

44 rters (CCCs) are responsible for the coupled co-transport of Cl(-) with K(+) and/or Na(+) in an elect

45 melibiose permease (MelB(St)) catalyzes the co-transport of galactosides with cations (H(+), Li(+),

46 hat relies exclusively or mainly on GLUT for co-transport of glucose and DHA including neurons, epith

47 The transport mechanism involves co-transport of glutamic acid with three Na(+) ions foll

48 The uptake of C3G by AtABCC2 depended on the co-transport of glutathione (GSH).

49 DASS from Vibrio cholerae that catalyses the co-transport of Na(+) and succinate.

50 reasoned that the N723S mutant may alter the co-transport of Nrxn1alpha at axonal processes to presyn

51 a dimer but only the Gpd1 dimer facilitates co-transport of Pnc1 into peroxisomes.

52 Importantly, a strictly substrate dependent co-transport of protons was also observed in in vitro tr

53 nsporters facilitate potassium uptake by the co-transport of protons.

54 Using two-color imaging we demonstrate co-transport of Rab11A and IAV vRNA in infected cells an

55 ke up glutamate into the cell, driven by the co-transport of sodium ions down their transmembrane con

56 ansmitters from the synapse, assisted by the co-transport of sodium ions.

57 cid transport by the EAATs is coupled to the co-transport of three Na(+) ions and one proton, and the

58 y amino acid carrier 1 (EAAC1) catalyzes the co-transport of three Na(+) ions, one H(+) ion, and one

59 cells is energetically driven by coupling to co-transport of three Na(+) ions.

60 to the cytoplasm, which could facilitate the co-transport of two cationic species.

61 mechanism is likely to be either folate/H(+) co-transport or folate/OH(-) exchange.

62 ressing the HBV receptor sodium taurocholate co-transporting polypeptide (NTCP) after lentiviral tran

63 and efflux transporters, sodium taurocholate co-transporting polypeptide (NTCP) and the bile salt exp

64 ocholate (TC) uptake and sodium taurocholate co-transporting polypeptide (Ntcp) translocation in hepa

65 to the receptor protein, Na(+)/taurocholate co-transporting polypeptide (NTCP), and for the subseque

66 hepatobiliary transporter Na(+)-taurocholate co-transporting polypeptide (NTCP).

67 kidney clones co-expressing Na+-taurocholate co-transporting polypeptide (Ntcp).

68 ues of the HBV receptor, sodium taurocholate co-transporting polypeptide (NTCP).

69 c bile acid importer, the Na(+)/taurocholate co-transporting polypeptide (Ntcp, Slc10a1).

70 epatic recirculation, the Na(+)-taurocholate co-transporting polypeptide (NTCP; also known as SLC10A1

71 tudies indicated that 17 is an organic anion co-transporting polypeptide 1B1 (OATP1B1) substrate.

72 B virus and its receptor Na(+)/taurocholate co-transporting polypeptide that can be used for structu

73 The CO transport process is not due to gas-phase transport b

74 The ligand (CO) transport process involves an initial, small amplitu

75 embrane proteins, including sodium-phosphate co-transport protein 2A (NPT2A) at the plasma membrane.

76 Membrane co-transport proteins that use a five-helix inverted rep

77 lease, as well as that of coupling to sodium co-transport, remain largely unknown for this important

78 he increase in GABA-evoked current, ion/GABA co-transport remained tightly coupled.

79 s (S1 for substrate, and Na1 and Na2 for two co-transported sodium ions) have been resolved, we still

80 SGLT1-mediated Na-glucose co-transport stimulates NHE3 activity in vivo by an Akt-

81 In contrast, in crypt cells, Na-glutamine co-transport stimulation was reversed to normal levels b

82 rotransmitter released into the synapse in a co-transport (symport) mechanism driven by the Na(+) ele

83 We show that calsyntenin-1 and APP are co-transported through axons and that siRNA-induced loss

84 ately 10 nm diameter nanostructures and that CO transports to Pt adsorption sites by an activated sur

85 illing, suggesting that these sequences were co-transported to the cytosol.

86 PS1 binds Notch in the ER/Golgi and is then co-transported to the plasma membrane as a complex.

87 Jip3 and Ret51 were also retrogradely co-transported, ultimately suggesting Jip3 is a retrogra

88 For motor pairs from both species, the co-transport velocities very nearly matched the single-m

89 PLC activity and sodium-dependent phosphate co-transport were essentially abolished.

90 Tau protein suggest motor protein-dependent co-transport with microtubule fragments and diffusion of

91 tion along neurites and at neurite tips, and co-transport with ribosomes, with beta-actin mRNA locali

92 nhancement with hydrophobicity indicated PAH co-transport with the motile organisms.

93 RV-G pseudotyped vectors were co-transported with both the tetanus neurotoxin-binding

94 eptide stoichiometry of 3:1, di-peptides are co-transported with either 4 or 5 protons.

95 The delivery of Pi to the mitochondrion, co-transported with protons, is required for oxidative p

96 nd by osmotic steps indicates that water was co-transported with sugar.

97 rmination, are selectively recruited by, and co-transported with, localizing transcripts in blastoder