BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 9571243)

  • 1. Lumenal and transmembrane domains play a role in sorting type I membrane proteins on endocytic pathways.
    Reaves BJ; Banting G; Luzio JP
    Mol Biol Cell; 1998 May; 9(5):1107-22. PubMed ID: 9571243
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Specificity of interaction between adaptor-complex medium chains and the tyrosine-based sorting motifs of TGN38 and lgp120.
    Stephens DJ; Banting G
    Biochem J; 1998 Nov; 335 ( Pt 3)(Pt 3):567-72. PubMed ID: 9794796
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cytoplasmic determinants involved in direct lysosomal sorting, endocytosis, and basolateral targeting of rat lgp120 (lamp-I) in MDCK cells.
    Höning S; Hunziker W
    J Cell Biol; 1995 Feb; 128(3):321-32. PubMed ID: 7844146
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The NH(2)-terminal transmembrane and lumenal domains of LGP85 are needed for the formation of enlarged endosomes/lysosomes.
    Kuronita T; Hatano T; Furuyama A; Hirota Y; Masuyama N; Saftig P; Himeno M; Fujita H; Tanaka Y
    Traffic; 2005 Oct; 6(10):895-906. PubMed ID: 16138903
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Efficient trafficking of TGN38 from the endosome to the trans-Golgi network requires a free hydroxyl group at position 331 in the cytosolic domain.
    Roquemore EP; Banting G
    Mol Biol Cell; 1998 Aug; 9(8):2125-44. PubMed ID: 9693371
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The targeting of Lamp1 to lysosomes is dependent on the spacing of its cytoplasmic tail tyrosine sorting motif relative to the membrane.
    Rohrer J; Schweizer A; Russell D; Kornfeld S
    J Cell Biol; 1996 Feb; 132(4):565-76. PubMed ID: 8647888
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chimeric forms of furin and TGN38 are transported with the plasma membrane in the trans-Golgi network via distinct endosomal pathways.
    Mallet WG; Maxfield FR
    J Cell Biol; 1999 Jul; 146(2):345-59. PubMed ID: 10465644
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lysosome associated membrane protein 1 (Lamp1) traffics directly from the TGN to early endosomes.
    Cook NR; Row PE; Davidson HW
    Traffic; 2004 Sep; 5(9):685-99. PubMed ID: 15296493
    [TBL] [Abstract][Full Text] [Related]  

  • 9. TGN38 recycles basolaterally in polarized Madin-Darby canine kidney cells.
    Rajasekaran AK; Humphrey JS; Wagner M; Miesenböck G; Le Bivic A; Bonifacino JS; Rodriguez-Boulan E
    Mol Biol Cell; 1994 Oct; 5(10):1093-103. PubMed ID: 7865877
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A dileucine motif and a cluster of acidic amino acids in the second cytoplasmic domain of the batten disease-related CLN3 protein are required for efficient lysosomal targeting.
    Storch S; Pohl S; Braulke T
    J Biol Chem; 2004 Dec; 279(51):53625-34. PubMed ID: 15469932
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The pathway and targeting signal for delivery of the integral membrane glycoprotein LEP100 to lysosomes.
    Mathews PM; Martinie JB; Fambrough DM
    J Cell Biol; 1992 Sep; 118(5):1027-40. PubMed ID: 1512288
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Protein targeting by tyrosine- and di-leucine-based signals: evidence for distinct saturable components.
    Marks MS; Woodruff L; Ohno H; Bonifacino JS
    J Cell Biol; 1996 Oct; 135(2):341-54. PubMed ID: 8896593
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Transport of the lysosomal membrane glycoprotein lgp120 (lgp-A) to lysosomes does not require appearance on the plasma membrane.
    Harter C; Mellman I
    J Cell Biol; 1992 Apr; 117(2):311-25. PubMed ID: 1560028
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Role of adaptor complex AP-3 in targeting wild-type and mutated CD63 to lysosomes.
    Rous BA; Reaves BJ; Ihrke G; Briggs JA; Gray SR; Stephens DJ; Banting G; Luzio JP
    Mol Biol Cell; 2002 Mar; 13(3):1071-82. PubMed ID: 11907283
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sorting of mannose 6-phosphate receptors and lysosomal membrane proteins in endocytic vesicles.
    Geuze HJ; Stoorvogel W; Strous GJ; Slot JW; Bleekemolen JE; Mellman I
    J Cell Biol; 1988 Dec; 107(6 Pt 2):2491-501. PubMed ID: 2849607
    [TBL] [Abstract][Full Text] [Related]  

  • 16. TGN38-green fluorescent protein hybrid proteins expressed in stably transfected eukaryotic cells provide a tool for the real-time, in vivo study of membrane traffic pathways and suggest a possible role for ratTGN38.
    Girotti M; Banting G
    J Cell Sci; 1996 Dec; 109 ( Pt 12)():2915-26. PubMed ID: 9013339
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Syntaxin 7 mediates endocytic trafficking to late endosomes.
    Nakamura N; Yamamoto A; Wada Y; Futai M
    J Biol Chem; 2000 Mar; 275(9):6523-9. PubMed ID: 10692457
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Derived protein sequence, oligosaccharides, and membrane insertion of the 120-kDa lysosomal membrane glycoprotein (lgp120): identification of a highly conserved family of lysosomal membrane glycoproteins.
    Howe CL; Granger BL; Hull M; Green SA; Gabel CA; Helenius A; Mellman I
    Proc Natl Acad Sci U S A; 1988 Oct; 85(20):7577-81. PubMed ID: 3174652
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The tyrosine-based lysosomal targeting signal in lamp-1 mediates sorting into Golgi-derived clathrin-coated vesicles.
    Höning S; Griffith J; Geuze HJ; Hunziker W
    EMBO J; 1996 Oct; 15(19):5230-9. PubMed ID: 8895568
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lysosomal targeting of Limp II membrane glycoprotein requires a novel Leu-Ile motif at a particular position in its cytoplasmic tail.
    Ogata S; Fukuda M
    J Biol Chem; 1994 Feb; 269(7):5210-7. PubMed ID: 8106503
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.