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140 related items for PubMed ID: 22537104
1. A critical histidine residue within LIMP-2 mediates pH sensitive binding to its ligand β-glucocerebrosidase. Zachos C, Blanz J, Saftig P, Schwake M. Traffic; 2012 Aug; 13(8):1113-23. PubMed ID: 22537104 [Abstract] [Full Text] [Related]
2. Disease-causing mutations within the lysosomal integral membrane protein type 2 (LIMP-2) reveal the nature of binding to its ligand beta-glucocerebrosidase. Blanz J, Groth J, Zachos C, Wehling C, Saftig P, Schwake M. Hum Mol Genet; 2010 Feb 15; 19(4):563-72. PubMed ID: 19933215 [Abstract] [Full Text] [Related]
3. LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of beta-glucocerebrosidase. Reczek D, Schwake M, Schröder J, Hughes H, Blanz J, Jin X, Brondyk W, Van Patten S, Edmunds T, Saftig P. Cell; 2007 Nov 16; 131(4):770-83. PubMed ID: 18022370 [Abstract] [Full Text] [Related]
4. A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome. Balreira A, Gaspar P, Caiola D, Chaves J, Beirão I, Lima JL, Azevedo JE, Miranda MC. Hum Mol Genet; 2008 Jul 15; 17(14):2238-43. PubMed ID: 18424452 [Abstract] [Full Text] [Related]
5. Lysosomal integral membrane protein-2: a new player in lysosome-related pathology. Gonzalez A, Valeiras M, Sidransky E, Tayebi N. Mol Genet Metab; 2014 Feb 15; 111(2):84-91. PubMed ID: 24389070 [Abstract] [Full Text] [Related]
6. A novel SCARB2 mutation in progressive myoclonus epilepsy indicated by reduced β-glucocerebrosidase activity. Zeigler M, Meiner V, Newman JP, Steiner-Birmanns B, Bargal R, Sury V, Mengistu G, Kakhlon O, Leykin I, Argov Z, Abramsky O, Lossos A. J Neurol Sci; 2014 Apr 15; 339(1-2):210-3. PubMed ID: 24485911 [Abstract] [Full Text] [Related]
8. Progressive myoclonus epilepsy with nephropathy C1q due to SCARB2/LIMP-2 deficiency: clinical report of two siblings. Chaves J, Beirão I, Balreira A, Gaspar P, Caiola D, Sá-Miranda MC, Lima JL. Seizure; 2011 Nov 15; 20(9):738-40. PubMed ID: 21782476 [Abstract] [Full Text] [Related]
9. Lysosome sorting of β-glucocerebrosidase by LIMP-2 is targeted by the mannose 6-phosphate receptor. Zhao Y, Ren J, Padilla-Parra S, Fry EE, Stuart DI. Nat Commun; 2014 Jul 14; 5():4321. PubMed ID: 25027712 [Abstract] [Full Text] [Related]
10. Lysosomal integral membrane protein type-2 (LIMP-2/SCARB2) is a substrate of cathepsin-F, a cysteine protease mutated in type-B-Kufs-disease. Peters J, Rittger A, Weisner R, Knabbe J, Zunke F, Rothaug M, Damme M, Berkovic SF, Blanz J, Saftig P, Schwake M. Biochem Biophys Res Commun; 2015 Feb 13; 457(3):334-40. PubMed ID: 25576872 [Abstract] [Full Text] [Related]
11. Characterization of the complex formed by β-glucocerebrosidase and the lysosomal integral membrane protein type-2. Zunke F, Andresen L, Wesseler S, Groth J, Arnold P, Rothaug M, Mazzulli JR, Krainc D, Blanz J, Saftig P, Schwake M. Proc Natl Acad Sci U S A; 2016 Apr 05; 113(14):3791-6. PubMed ID: 27001828 [Abstract] [Full Text] [Related]
12. Hyperacidification of trans-Golgi network and endo/lysosomes in melanocytes by glucosylceramide-dependent V-ATPase activity. van der Poel S, Wolthoorn J, van den Heuvel D, Egmond M, Groux-Degroote S, Neumann S, Gerritsen H, van Meer G, Sprong H. Traffic; 2011 Nov 05; 12(11):1634-47. PubMed ID: 21810155 [Abstract] [Full Text] [Related]
13. Tubular proteinuria in mice and humans lacking the intrinsic lysosomal protein SCARB2/Limp-2. Desmond MJ, Lee D, Fraser SA, Katerelos M, Gleich K, Martinello P, Li YQ, Thomas MC, Michelucci R, Cole AJ, Saftig P, Schwake M, Stapleton D, Berkovic SF, Power DA. Am J Physiol Renal Physiol; 2011 Jun 05; 300(6):F1437-47. PubMed ID: 21429972 [Abstract] [Full Text] [Related]
14. The LIMP-2/SCARB2 binding motif on acid β-glucosidase: basic and applied implications for Gaucher disease and associated neurodegenerative diseases. Liou B, Haffey WD, Greis KD, Grabowski GA. J Biol Chem; 2014 Oct 24; 289(43):30063-74. PubMed ID: 25202012 [Abstract] [Full Text] [Related]
15. Mannose 6-phosphate-independent Lysosomal Sorting of LIMP-2. Blanz J, Zunke F, Markmann S, Damme M, Braulke T, Saftig P, Schwake M. Traffic; 2015 Oct 24; 16(10):1127-36. PubMed ID: 26219725 [Abstract] [Full Text] [Related]
16. Lysosomal membrane proteins: life between acid and neutral conditions. Saftig P, Schröder B, Blanz J. Biochem Soc Trans; 2010 Dec 24; 38(6):1420-3. PubMed ID: 21118100 [Abstract] [Full Text] [Related]
17. [Advances in research of SCARB2 functions and related disorders]. He M, Liu Z, Tang B, Wang J. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Oct 24; 32(5):723-7. PubMed ID: 26419000 [Abstract] [Full Text] [Related]
18. A shortcut to the lysosome: the mannose-6-phosphate-independent pathway. Coutinho MF, Prata MJ, Alves S. Mol Genet Metab; 2012 Nov 24; 107(3):257-66. PubMed ID: 22884962 [Abstract] [Full Text] [Related]
19. Localization of active endogenous and exogenous β-glucocerebrosidase by correlative light-electron microscopy in human fibroblasts. van Meel E, Bos E, van der Lienden MJC, Overkleeft HS, van Kasteren SI, Koster AJ, Aerts JMFG. Traffic; 2019 May 24; 20(5):346-356. PubMed ID: 30895685 [Abstract] [Full Text] [Related]
20. V-ATPase interacts with ARNO and Arf6 in early endosomes and regulates the protein degradative pathway. Hurtado-Lorenzo A, Skinner M, El Annan J, Futai M, Sun-Wada GH, Bourgoin S, Casanova J, Wildeman A, Bechoua S, Ausiello DA, Brown D, Marshansky V. Nat Cell Biol; 2006 Feb 24; 8(2):124-36. PubMed ID: 16415858 [Abstract] [Full Text] [Related] Page: [Next] [New Search]