ライフサイエンスコーパス: vacuolar type

1 Vesicular- or vacuolar-type adenosine triphosphatases (V-ATPases) are

2 Vacuolar-type adenosine triphosphatases (V-ATPases) are

3 Vacuolar-type adenosine triphosphatases (V-ATPases)(1-3)

4 ses energy from proton-pumping vesicular- or vacuolar-type adenosine triphosphatases (V-ATPases).

5 Vacuolar type ATPase (V-ATPase) has recently emerged as

6 ification of synaptic vesicles relies on the vacuolar-type ATPase (V-ATPase) and provides the electro

7 , we demonstrate that inhibition of the H(+) vacuolar-type ATPase (V-ATPase) caused drastic cell swel

8 The vacuolar-type ATPase (V-ATPase) is a proton pump compose

9 cells show impaired cleavage or shedding of vacuolar-type ATPase (V-ATPase) subunits Ac45 and proren

10 cells show impaired cleavage or shedding of vacuolar-type ATPase (V-ATPase) subunits Ac45 and proren

11 the antitumor activity of inhibitors of the vacuolar-type ATPase (V-ATPase), a heteromultimeric prot

12 ied the existence of a specific 'epithelial' vacuolar-type ATPase configuration.

13 Instead, an H+ translocating, vacuolar-type ATPase generates a voltage of approximatel

14 xpression of a family of proton-transporting vacuolar-type ATPase subtypes in the development of imGC

15 ion is strictly dependent on the function of vacuolar type-ATPase.

16 Vacuolar type ATPases (V-type ATPases) are highly conser

17 Vacuolar-type ATPases (V-ATPases) are ATP-powered proton

18 Vacuolar-type ATPases (V-ATPases) are membrane-embedded

19 Proton-translocating vacuolar-type ATPases (V-ATPases) are necessary for nume

20 Vacuolar-type ATPases (V-ATPases) exist in various cellu

21 Based upon the precedent of the subunit c in vacuolar-type ATPases, which are composed of four transm

22 This vacuolar-type Ca(2+)-ATPase could play an important role

23 Vacuolar type H(+) V-ATPase (VHA) in the endothelium aci

24 ipropylamine and stained weakly positive for vacuolar type H+ ATPase.

25 etreatment of oocytes with bafilomycin A1, a vacuolar type H+-ATPase inhibitor, abolished the increas

26 Vacuolar-type H(+) ATPase (VHA) protein is highly expres

27 afficking of soluble proteins, requires both vacuolar-type H(+) ATPase-dependent acidification as wel

28 ies have suggested that the V0 domain of the vacuolar-type H(+)-adenosine triphosphatase (V-ATPase) i

29 Without actin, lysosomes never recycle vacuolar-type H(+)-adenosine triphosphatase (V-ATPase) o

30 We show that the neuronal vacuolar-type H(+)-adenosine triphosphatase V0 subunit a

31 at the regulation occurs on the level of the vacuolar-type H(+)-adenosine triphosphatase.

32 and expression of the proton pumping enzyme vacuolar-type H(+)-adenosine triphosphatase.

33 scle has disclosed the endosomal proton pump vacuolar-type H(+)-ATPase (v-ATPase) as a key enzyme reg

34 Pharmacological inhibition of vacuolar-type H(+)-ATPase (V-ATPase) by its specific inh

35 clone encoding the c ("16 kDa') subunit of a vacuolar-type H(+)-ATPase (V-ATPase) from Kalanchoe daig

36 fication of endomembrane compartments by the vacuolar-type H(+)-ATPase (V-ATPase) is central to many

37 y and polarity-dependent localization of the vacuolar-type H(+)-ATPase (V-ATPase) mediate the impact

38 quality control factors - is the loss of the vacuolar-type H(+)-ATPase (v-ATPase), a key regulator of

39 by 25 microm bafilomycin-A1, an inhibitor of vacuolar-type H(+)-ATPase (v-ATPase), which actively pum

40 rom inhibition of proton pumping activity of vacuolar-type H(+)-ATPase (v-ATPase).

41 eceptor signaling, postsynaptic calcium, and vacuolar-type H(+)-ATPase activity in the postsynaptic c

42 but is not dependent on Na(+)-H+ exchange or vacuolar-type H(+)-ATPase activity.

43 ctor binds to the conserved Vo domain of the vacuolar-type H(+)-ATPase and causes deacidification of

44 Here, we show strong evidence that vacuolar-type H(+)-ATPase and plasma-accessible carbonic

45 Mutations in the vacuolar-type H(+)-ATPase B1 subunit gene ATP6V1B1 cause

46 ltaneously, MDMs increased the expression of vacuolar-type H(+)-ATPase components, acidified the peri

47 ng of phagosomal acidification by inhibiting vacuolar-type H(+)-ATPase enabled macrophages to elicit

48 ake in vesicles, because bafilomycin A(1), a vacuolar-type H(+)-ATPase inhibitor, reduced glutamate r

49 din B is structurally similar to more potent vacuolar-type H(+)-ATPase inhibitors, which all inhibite

50 Proton pumping of the vacuolar-type H(+)-ATPase into the lumen of the central

51 CO2 Bafilomycin A1, a specific inhibitor of vacuolar-type H(+)-ATPase that blocks lysosomal degradat

52 et membranes dictate its preference for host vacuolar-type H(+)-ATPase-containing membranes, indicati

53 e electrochemical gradient maintained by the vacuolar-type H(+)-ATPase.

54 The vacuolar-type H(+)-ATPases (V-ATPase) hydrolyze ATP to p

55 Vacuolar-type H(+)-ATPases (V-ATPases) contribute to pH

56 Vacuolar-type H(+)-ATPases (V-H(+)-ATPases) are the majo

57 ication of intracellular compartments by the vacuolar-type H(+)-ATPases (VHA) is known to energize io

58 e isolation and characterization of a type I vacuolar-type H(+)-pyrophosphatase (V-PPase), TgVP1, fro

59 The general consensus is that the vacuolar-type H(+)-translocating ATPase (V-ATPase) is cr

60 determinant of acidic pH at the Golgi is the vacuolar-type H(+)-translocating ATPase (V-ATPase), whos

61 The multisubunit vacuolar-type H(+)ATPases mediate acidification of vario

62 expression of one particular subunit of the vacuolar-type H+ ATPase (V-ATPase), which is responsible

63 Vacuolar-type H+-ATPase (V-ATPase) and calcineurin (Cn)

64 Vacuolar-type H+-ATPase (V-ATPase) is a multimeric compl

65 Vacuolar-type H+-ATPase was not colocalized with HGE age

66 ry of recurrent mutations in subunits of the vacuolar-type H+-translocating ATPase (v-ATPase) in foll

67 Vacuolar-type H+-translocating ATPases (V-ATPases or V-p

68 The vacuolar-type H+-transporting ATPase (V-ATPase), rather

69 imary murine CTLs that the a3-subunit of the vacuolar-type (H(+))-adenosine triphosphatase is require

70 The presence of the vacuolar-type (H+) ATPase (V-ATPase) within the Coxiella

71 filomycin, consistent with a major role of a vacuolar-type (H+)-ATPase in this process.

72 ept those with deletions of YCK3, encoding a vacuolar type I casein kinase; SVP26, encoding an endopl

73 Secreted A1AT carried vacuolar-type paucimannosidic N-glycans generated by the

74 The gene encoding the vacuolar-type proteolipid of the V-ATPase from Giardia l

75 ribution of the conserved residues among the vacuolar-type proteolipids suggest a zipper-type interac

76 The vacuolar type proton pump of clathrin-coated vesicles ha

77 era raised against a peptide sequence of the vacuolar type proton pyrophosphatase (H(+)-PPase) of Ara

78 The vacuolar type proton-translocating ATPase of clathrin-co

79 However, it affects vacuolar-type proton ATPase (V-ATPase) activity, thereby

80 The vacuolar-type proton pump of clathrin-coated vesicles is

81 oton gradient maintained by an ATP-dependent vacuolar-type proton pump.

82 erently to osmotic challenges, they both use vacuolar-type proton pumps for filling contractile vacuo

83 r assembly with the catalytic sector (V1) of vacuolar-type proton translocating ATPase (V-ATPase) and

84 Because vacuolar-type proton-pump-dependent contractile vacuole

85 idic calcium store in trypanosomatids with a vacuolar-type proton-pumping pyrophosphatase (V-H(+)-PPa

86 The multisubunit vacuolar-type proton-translocating ATPases (H(+)-ATPases

87 The vacuolar-type proton-translocating pyrophosphatase (V-H+

88 The vacuolar-type, proton-translocating ATPase (V-ATPase) is

89 Subunit a of the yeast vacuolar-type, proton-translocating ATPase enzyme comple

90 (Baf), a potent and specific blocker of the vacuolar-type (V-type) ATPase, which eliminates the driv

91 The membrane rotor ring from the vacuolar-type (V-type) sodium ion-pumping adenosine trip