ライフサイエンスコーパス: lysosome-associated membrane protein

1 oglobulin family receptors (e.g., CD44), and lysosome-associated membrane protein.

2 SifA recruits membranes enriched in lysosome associated membrane protein 1 (LAMP1) and is ne

3 In HPS-1, lysosome associated membrane protein 1 (LAMP1), and LAMP

4 ugh phagosomes from both cell types acquired lysosome-associated membrane protein 1 (LAMP-1) and MHC-

5 early endosome antigen 1 (EEA1) followed by lysosome-associated membrane protein 1 (LAMP-1), with pe

6 propose that MDV trafficking is mediated by lysosome-associated membrane protein 1 (LAMP-1)-positive

7 lemental mixture were more likely to contain lysosome-associated membrane protein 1 (LAMP-1).

8 afficking of tyrosinase-related proteins and lysosome-associated membrane protein 1 (Lamp-1).

9 IgaB cleaves lysosome-associated membrane protein 1 (LAMP1) at pHs ch

10 ced by intracellular bacteria also contained lysosome-associated membrane protein 1 (LAMP1), suggesti

11 lized tetherin is sequestered in a CD63- and lysosome-associated membrane protein 1 (LAMP1)-positive

12 compartment, followed by colocalization with lysosome-associated membrane protein 1 (LAMP1)-positive

13 idase (APEX) gene to the endogenous locus of lysosome-associated membrane protein 1 (LAMP1).

14 , including alpha-dystroglycan (alphaDG) and lysosome-associated membrane protein 1 (LAMP1).

15 However, they universally recruit lysosome-associated membrane protein 1 (LAMP1); the mech

16 A phagosomal integrity assay and lysosome-associated membrane protein 1 colocalization re

17 Lysosome-associated membrane protein 1 immunostaining an

18 ichia spp. were not labeled with either anti-lysosome-associated membrane protein 1 or anti-CD63.

19 Colocalization of Tyr with lysosome-associated membrane protein 1 was observed with

20 resulted in the loss of CD1d trafficking to lysosome-associated membrane protein 1(+) compartments.

21 t the Neisseria IgA1 protease cleaves LAMP1 (lysosome-associated membrane protein 1), a major integra

22 tions in neurons [beta-hexosaminidase, LAMP1(lysosome-associated membrane protein 1), SCMAS (subunit

23 The localization of internalized BCR to lysosome-associated membrane protein 1-positive late end

24 sE mutants were shown to undergo escape from lysosome-associated membrane protein 1-positive vacuoles

25 nfection, PCPLC colocalized with bacteria in lysosome-associated membrane protein 1-positive vacuoles

26 e CCR10/eNOS complex and colocalization with lysosome-associated membrane protein 1.

27 fected cells, as shown by immunostaining for lysosome-associated membrane protein 1.

28 Cells displayed increased surface MPRs and lysosome-associated membrane protein 1.

29 S did not acquire certain lysosomal markers (lysosome-associated membrane protein 1/2) but were posit

30 DC transfected with mRNA encoding a chimeric lysosome-associated membrane protein-1 (LAMP) hTERT prot

31 dly increased co-localization of mTORC1 with lysosome-associated membrane protein-1 (Lamp-1) (lysosom

32 Indeed, surface staining of lysosome-associated membrane protein-1 (Lamp-1) was dram

33 analysis showed that MTB phagosomes acquired lysosome-associated membrane protein-1 (LAMP-1), MHC-II,

34 with the eight COOH-terminal amino acids of lysosome-associated membrane protein-1 (TL).

35 e endosomes and lysosomes (labeled with anti-lysosome-associated membrane protein-1 [LAMP-1]), were r

36 By contrast, lysosome-associated membrane protein-1 distribution was

37 ociated protein 1 light chain 3B (LC3B) with lysosome-associated membrane protein-1, increased levels

38 d beclin 1) and effectors (LC3 and p62), and lysosome-associated membrane protein 2 (LAMP2) was obser

39 In the remaining 35 patients, PRKAG2, lysosome-associated membrane protein 2 (LAMP2), alpha-ga

40 with PX-866 increased protein levels of p62, lysosome-associated membrane protein 2 (LAMP2), and micr

41 n the late endosomal/lysosomal compartments (lysosome-associated membrane protein 2 (LAMP2)-positive)

42 the lysosomal abundance of the CMA receptor, lysosome-associated membrane protein 2 A (LAMP2A).

43 associated protein 1A/1B light chains 3, and lysosome-associated membrane protein 2.

44 a high frequency of autoantibodies to human lysosome-associated membrane protein-2 (hLAMP-2) in ANCA

45 The involvement of autoantibodies to human lysosome-associated membrane protein-2 (hLAMP-2) in anti

46 Several conserved isoforms of the lysosome-associated membrane protein-2 (LAMP-2) regulate

47 d in cells with diminished expression of the lysosome-associated membrane protein-2 (Lamp-2).

48 NPC1 gene product resides in a novel set of lysosome-associated membrane protein-2 (LAMP2)(+)/mannos

49 y reactive oxygen species-induced decline in lysosome-associated membrane protein-2 and upregulation

50 Restoration of lysosome-associated membrane protein-2 levels synergizes

51 ted BECLIN-1 upregulation and a reduction in lysosome-associated membrane protein-2, a critical deter

52 ated membrane protein-1, increased levels of lysosome-associated membrane protein-2, and increased ma

53 Vangl2 directly binds to lysosome-associated membrane protein 2A (LAMP-2A) and ta

54 observe that the autophagy markers LC3b and lysosome-associated membrane protein 2A (LAMP2A) localiz

55 Such treatment did not affect the levels of lysosome-associated membrane protein 2a or lysosomal hea

56 Previous studies showed that lysosome-associated membrane protein 3 (LAMP3) overexpre

57 patients identified increased expression of lysosome-associated membrane protein 3 (LAMP3/CD208/DC-L

58 cules as well as the DC maturation marker DC-lysosome-associated membrane protein, and they stimulate

59 orescence microscopic analysis using an anti-lysosome-associated membrane protein antibody identified

60 feron and showed increased expression of the lysosome-associated membrane protein CD107a on the cell

61 Mutations in X-linked lysosome-associated membrane protein gene (LAMP2; Danon

62 wild-type CLN3, were highly associated with lysosome-associated membrane protein II in non-neuronal

63 ation of LC3B paralogues and diminishment of lysosome associated membrane protein (LAMP)-1, LAMP-2 an

64 Lysosome-associated membrane protein (LAMP) 1/CD107a is

65 Using staining for the lysosome-associated membrane protein (LAMP) and by pharm

66 afficking of lysosomal membrane proteins via lysosome-associated membrane protein (LAMP) carriers fro

67 d with L. pneumophila, and then the acidity, lysosome-associated membrane protein (LAMP) content, and

68 The lysosome-associated membrane protein (LAMP) family inclu

69 nes encoding antigen chimeras containing the lysosome-associated membrane protein (LAMP) translocon,

70 h age because of a decrease in the levels of lysosome-associated membrane protein (LAMP) type 2A, a l

71 Cs showed impaired expression of CD83 and DC-lysosome-associated membrane protein (LAMP), low levels

72 monomeric CpG-B oligonucleotides localize to lysosome-associated membrane protein (LAMP)-1-positive e

73 was employed to study the function of p67, a lysosome-associated membrane protein (LAMP)-like type I

74 gosome-lysosome fusion was scored using both lysosome-associated membrane protein (LAMP-1) as a membr

75 nsfected with mRNA encoding a chimeric hTERT/lysosome-associated membrane protein (LAMP-1) protein, c

76 essing, we linked the sorting signals of the lysosome-associated membrane protein (LAMP-1) to the cyt

77 lved in cholesterol export from LEs, and the lysosome-associated membrane proteins (LAMP) 1 and 2 are

78 The lysosome-associated membrane proteins (LAMP), found in t

79 The extensively glycosylated lysosome-associated membrane proteins (LAMP)-2a, b, and

80 aining glycoproteins (Man 6-P GP) but little lysosome-associated membrane proteins (LAMP).

81 o unravel a key biological function of human lysosome-associated membrane proteins (LAMP-1 and LAMP-2

82 Unexpectedly, the lysosome-associated membrane proteins, LAMP1 and LAMP2,

83 pendent mannose 6-phosphate receptor and the lysosome-associated membrane proteins (LAMPs) 1 and 2.

84 a group of transmembrane glycoproteins named lysosome-associated membrane proteins (Lamps).

85 The lysosome-associated membrane protein LGP110 did not co-l

86 ome mobility, as well as accumulation of the lysosome-associated membrane protein LMP-1.

87 ing HIV-1 gag p24 do not express CD83 and DC-lysosome-associated membrane protein maturation markers.

88 These include detecting the appearance of lysosome-associated membrane protein on the cell's surfa

89 with the late endosomal and lysosomal marker lysosome-associated membrane protein revealed that fusio

90 with cDNA for HA flanked by sequences of the lysosome-associated membrane protein that direct efficie

91 , calreticulin, or the sorting signal of the lysosome-associated membrane protein type 1 (LAMP-1), en

92 rategies tested, mice vaccinated with Sig/E7/lysosome-associated membrane protein type 1 mixed with S

93 ing treatment with CpG ODN, TLR9 is found in lysosome-associated membrane protein type 1-positive lys

94 osa exotoxin A, or the sorting signal of the lysosome-associated membrane protein type 1.

95 shock cognate protein of 70 kDa (HSC70) and lysosome-associated membrane protein type 2 A (LAMP2A),

96 Components of CMA, namely the lysosome-associated membrane protein type 2A (LAMP-2A) a

97 was paralleled by a marked elevation of the lysosome-associated membrane protein type 2A (LAMP-2A) a

98 The lysosome-associated membrane protein type 2a (LAMP-2A) t

99 s bind to the lysosomal membrane through the lysosome-associated membrane protein type 2A (LAMP-2A),

100 utophagy is the binding of substrates to the lysosome-associated membrane protein type 2A (LAMP-2A).

101 ase activity triggers the degradation of the lysosome-associated membrane protein type 2a (lamp2a), a

102 mune system, due to a reduction in levels of lysosome-associated membrane protein type 2A (LAMP2A), a

103 A decrease in lysosomal levels of the lysosome-associated membrane protein type 2A (LAMP2A), t

104 ve age-related decrease in the levels of the lysosome-associated membrane protein type 2a that acts a

105 This accelerated degradation of lysosome-associated membrane protein type 2A, also descr

106 rease in the levels of the CMA receptor, the lysosome-associated membrane protein type 2A, because of

107 and increased glycosylation and stability of lysosome-associated membrane proteins, which are known t