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

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

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

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

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

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

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

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

14 Lysosome-associated membrane protein 1 immunostaining an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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