ライフサイエンスコーパス: inner face

1 e was modeled as a box with receptors on one inner face.

2 logy, with a longer outer face and a shorter inner face.

3 rial insertions into the outer face than the inner face.

4 mbranes and severs membrane necks from their inner face.

5 The salience of inner face components was enhanced by presenting them in

6 recombinant MAOA is situated on the opposite inner face in Pichia mitochondria.

7 s, on average, 5-10 ribbon synapses with the inner face of a calyx ending.

8 CrvA self-assembles into filaments at the inner face of cell curvature.

9 of nucleotides from the solution bathing the inner face of excised patches of frog atrial membranes w

10 t the G(Talpha) C-terminal tail binds to the inner face of helix 6 in a retinal-linked manner.

11 Syntaxin is anchored to the inner face of presynaptic plasma membrane via a single C

12 ly of spectrin and actin associated with the inner face of the axolemma, could be involved in bringin

13 eutralization of phosphate charges along the inner face of the bent double helix.

14 te GLUT4-containing vesicles adjacent to the inner face of the cell surface membrane but that was not

15 se activation specificity are located on the inner face of the core shell, distinct from the amino te

16 ther than to its ectopic localization at the inner face of the cytoplasmic membrane.

17 distinct subset of neurons positioned at the inner face of the dentate gyrus, whereas Abeta42 bound s

18 rticipate in hydrophobic interactions on the inner face of the flap; (iii) Ile-50 has hydrophobic int

19 urements indicate that a bimane label on the inner face of the helix (at V250C) detects changes in th

20 secretion of Yops and LcrV, possibly at the inner face of the inner membrane.

21 nctional subdomains; one associated with the inner face of the inner mitochondrial membrane and the o

22 out the cell cycle, predominantly around the inner face of the interphase SPB, adjacent to the nucleu

23 onine 56 is in direct contact with the re or inner face of the isoalloxazine ring of the FMN cofactor

24 ngly inhibited by application of Ca2+ to the inner face of the membrane (IC50 = 122 nM); this inhibit

25 phore, suggesting that direct binding to the inner face of the membrane accounts for the effects of c

26 ComGA, a putative ATPase, is located on the inner face of the membrane as a peripheral membrane prot

27 which presents a specific surface toward the inner face of the membrane that can interact to varying

28 by an increased rate of deprotonation on the inner face of the membrane, leading to an increase in th

29 n homology domain-containing proteins on the inner face of the membrane.

30 cause the N terminus remains anchored to the inner face of the membrane.

31 rmeability transition pore must occur at the inner face of the mitochondrial inner membrane.

32 counterions adsorption sites located on the inner face of the NT walls are responsible for this size

33 noelectron microscopy localized NUP-1 to the inner face of the nuclear envelope, suggesting that it i

34 However, this NES, located at the inner face of the PCNA trimer, was not functional in wil

35 minantly exists juxtaposed to and lining the inner face of the plasma membrane (cortical actin) with

36 the ligand binding site of TRPV1 lies on the inner face of the plasma membrane and that much of the T

37 ular systems, PLAC8 protein localizes to the inner face of the plasma membrane in pancreatic cancer c

38 RAC in D. discoideum to binding sites on the inner face of the plasma membrane reflects activation of

39 sent in the cortical granules located at the inner face of the plasma membrane.

40 aces of this half doughnut suggests that the inner face of the PUM-HD binds RNA while the outer face

41 oteins with disordered regions that line the inner face of the scaffold.

42 ssential and part of a stable network at the inner face of the trypanosome nuclear envelope, since kn

43 residues in specific protein surfaces of the inner face of the viral matrix and at the Cyclophilin A

44 x proteins are found in association with the inner face of the viral membrane.

45 th at least one curved region contacting the inner face of the viral membrane.

46 on to the MII form did residues found on the inner "face" of this helix react with the PyMPO-maleimid

47 ssed per afferent, there are, on average, 15 inner-face ribbon synapses, 0.38 outer-face ribbons, and

48 s are similar, reinforcing the importance of inner-face ribbons in synaptic transmission.

49 Inner-face synapses outnumber those on calyx outer faces