Mannose phosphorylation in health and disease

Kollmann K, Pohl S, Marschner K, Encarnacao M, Sakwa I, Tiede S, Poorthuis BJ, Lübke T, Müller-Loennies S, Storch S, Braulke T (2010)
European Journal of Cell Biology 89(1): 117-123.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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DOI
Autor*in
Kollmann, Katrin; Pohl, Sandra; Marschner, Katrin; Encarnacao, Marisa; Sakwa, Imme; Tiede, Stephan; Poorthuis, Ben J.; Lübke, TorbenUniBi ; Müller-Loennies, Sven; Storch, Stephan; Braulke, Thomas
Einrichtung
Fakultät für Chemie > Biochemie I
Erscheinungsjahr
2010
Zeitschriftentitel
European Journal of Cell Biology
Band
89
Ausgabe
1
Seite(n)
117-123
ISSN
0171-9335
Page URI
https://pub.uni-bielefeld.de/record/1939885

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Kollmann K, Pohl S, Marschner K, et al. Mannose phosphorylation in health and disease. European Journal of Cell Biology. 2010;89(1):117-123.
Kollmann, K., Pohl, S., Marschner, K., Encarnacao, M., Sakwa, I., Tiede, S., Poorthuis, B. J., et al. (2010). Mannose phosphorylation in health and disease. European Journal of Cell Biology, 89(1), 117-123. https://doi.org/10.1016/j.ejcb.2009.10.008
Kollmann, Katrin, Pohl, Sandra, Marschner, Katrin, Encarnacao, Marisa, Sakwa, Imme, Tiede, Stephan, Poorthuis, Ben J., et al. 2010. “Mannose phosphorylation in health and disease”. European Journal of Cell Biology 89 (1): 117-123.
Kollmann, K., Pohl, S., Marschner, K., Encarnacao, M., Sakwa, I., Tiede, S., Poorthuis, B. J., Lübke, T., Müller-Loennies, S., Storch, S., et al. (2010). Mannose phosphorylation in health and disease. European Journal of Cell Biology 89, 117-123.
Kollmann, K., et al., 2010. Mannose phosphorylation in health and disease. European Journal of Cell Biology, 89(1), p 117-123.
K. Kollmann, et al., “Mannose phosphorylation in health and disease”, European Journal of Cell Biology, vol. 89, 2010, pp. 117-123.
Kollmann, K., Pohl, S., Marschner, K., Encarnacao, M., Sakwa, I., Tiede, S., Poorthuis, B.J., Lübke, T., Müller-Loennies, S., Storch, S., Braulke, T.: Mannose phosphorylation in health and disease. European Journal of Cell Biology. 89, 117-123 (2010).
Kollmann, Katrin, Pohl, Sandra, Marschner, Katrin, Encarnacao, Marisa, Sakwa, Imme, Tiede, Stephan, Poorthuis, Ben J., Lübke, Torben, Müller-Loennies, Sven, Storch, Stephan, and Braulke, Thomas. “Mannose phosphorylation in health and disease”. European Journal of Cell Biology 89.1 (2010): 117-123.

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Bajaj L, Lotfi P, Pal R, Ronza AD, Sharma J, Sardiello M., J Neurochem 148(5), 2019
PMID: 30092616
TGF-ß Regulates Cathepsin Activation during Normal and Pathogenic Development.
Flanagan-Steet H, Christian C, Lu PN, Aarnio-Peterson M, Sanman L, Archer-Hartmann S, Azadi P, Bogyo M, Steet RA., Cell Rep 22(11), 2018
PMID: 29539424
The Lysosomal Protein Arylsulfatase B Is a Key Enzyme Involved in Skeletal Turnover.
Pohl S, Angermann A, Jeschke A, Hendrickx G, Yorgan TA, Makrypidi-Fraune G, Steigert A, Kuehn SC, Rolvien T, Schweizer M, Koehne T, Neven M, Winter O, Velho RV, Albers J, Streichert T, Pestka JM, Baldauf C, Breyer S, Stuecker R, Muschol N, Cox TM, Saftig P, Paganini C, Rossi A, Amling M, Braulke T, Schinke T., J Bone Miner Res 33(12), 2018
PMID: 30075049
Traffic from the endosome towards trans-Golgi network.
Saimani U, Kim K., Eur J Cell Biol 96(2), 2017
PMID: 28256269
Origin of α-mannosidase activity in CSF.
Tasegian A, Paciotti S, Ceccarini MR, Codini M, Moors T, Chiasserini D, Albi E, Winchester B, van de Berg WDJ, Parnetti L, Beccari T., Int J Biochem Cell Biol 87(), 2017
PMID: 28359775
Altered Met receptor phosphorylation and LRP1-mediated uptake in cells lacking carbohydrate-dependent lysosomal targeting.
Aarnio-Peterson M, Zhao P, Yu SH, Christian C, Flanagan-Steet H, Wells L, Steet R., J Biol Chem 292(36), 2017
PMID: 28724630
Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease.
Zrhidri A, Amasdl S, Lyahyai J, Elouardi H, Chkirate B, Raymond L, Egéa G, Taoudi M, El Mouatassim S, Sefiani A., Pediatr Rheumatol Online J 15(1), 2017
PMID: 28950892
Cathepsin-Mediated Alterations in TGFß-Related Signaling Underlie Disrupted Cartilage and Bone Maturation Associated With Impaired Lysosomal Targeting.
Flanagan-Steet H, Aarnio M, Kwan B, Guihard P, Petrey A, Haskins M, Blanchard F, Steet R., J Bone Miner Res 31(3), 2016
PMID: 26404503
Alteration of cathepsin D trafficking induced by hypoxia and extracellular acidification in MCF-7 breast cancer cells.
Achour O, Ashraf Y, Bridiau N, Kacem M, Poupard N, Bordenave-Juchereau S, Sannier F, Lamerant-Fayel N, Kieda C, Liaudet-Coopman E, Piot JM, Maugard T, Fruitier-Arnaudin I., Biochimie 121(), 2016
PMID: 26582416
Analysis of zwitterionic and anionic N-linked glycans from invertebrates and protists by mass spectrometry.
Paschinger K, Wilson IB., Glycoconj J 33(3), 2016
PMID: 26899268
Sweet complementarity: the functional pairing of glycans with lectins.
Gabius HJ, Manning JC, Kopitz J, André S, Kaltner H., Cell Mol Life Sci 73(10), 2016
PMID: 26956894
Identification of the interaction domains between α- and γ-subunits of GlcNAc-1-phosphotransferase.
Velho RV, De Pace R, Tidow H, Braulke T, Pohl S., FEBS Lett 590(23), 2016
PMID: 27736005
Subcellular Trafficking of Mammalian Lysosomal Proteins: An Extended View.
Staudt C, Puissant E, Boonen M., Int J Mol Sci 18(1), 2016
PMID: 28036022
Dried blood spots allow targeted screening to diagnose mucopolysaccharidosis and mucolipidosis.
Cobos PN, Steglich C, Santer R, Lukacs Z, Gal A., JIMD Rep 15(), 2015
PMID: 24798265
Exome sequencing for mucolipidosis III: Detection of a novel GNPTAB gene mutation in a patient with a very mild phenotype.
Sperb-Ludwig F, Alegra T, Velho RV, Ludwig N, Kim CA, Kok F, Kitajima JP, van Meel E, Kornfeld S, Burin MG, Schwartz IVD., Mol Genet Metab Rep 2(), 2015
PMID: 28649523
Cathepsin inhibition-induced lysosomal dysfunction enhances pancreatic beta-cell apoptosis in high glucose.
Jung M, Lee J, Seo HY, Lim JS, Kim EK., PLoS One 10(1), 2015
PMID: 25625842
Association study of stuttering candidate genes GNPTAB, GNPTG and NAGPA with dyslexia in Chinese population.
Chen H, Xu J, Zhou Y, Gao Y, Wang G, Xia J, Huen MS, Siok WT, Jiang Y, Tan LH, Sun Y., BMC Genet 16(), 2015
PMID: 25643770
Analyses of disease-related GNPTAB mutations define a novel GlcNAc-1-phosphotransferase interaction domain and an alternative site-1 protease cleavage site.
Velho RV, De Pace R, Klünder S, Sperb-Ludwig F, Lourenço CM, Schwartz IV, Braulke T, Pohl S., Hum Mol Genet 24(12), 2015
PMID: 25788519
Retromer-Mediated Trafficking of Transmembrane Receptors and Transporters.
Klinger SC, Siupka P, Nielsen MS., Membranes (Basel) 5(3), 2015
PMID: 26154780
Lysosomal integral membrane protein-2: a new player in lysosome-related pathology.
Gonzalez A, Valeiras M, Sidransky E, Tayebi N., Mol Genet Metab 111(2), 2014
PMID: 24389070
Mucolipidosis II-related mutations inhibit the exit from the endoplasmic reticulum and proteolytic cleavage of GlcNAc-1-phosphotransferase precursor protein (GNPTAB).
De Pace R, Coutinho MF, Koch-Nolte F, Haag F, Prata MJ, Alves S, Braulke T, Pohl S., Hum Mutat 35(3), 2014
PMID: 24375680
Introduction to glycopathology: the concept, the tools and the perspectives.
Gabius HJ, Kayser K., Diagn Pathol 9(), 2014
PMID: 24443956
Filter-aided N-glycan separation (FANGS): a convenient sample preparation method for mass spectrometric N-glycan profiling.
Abdul Rahman S, Bergström E, Watson CJ, Wilson KM, Ashford DA, Thomas JR, Ungar D, Thomas-Oates JE., J Proteome Res 13(3), 2014
PMID: 24450425
Molecular characterization of arylsulfatase G: expression, processing, glycosylation, transport, and activity.
Kowalewski B, Lübke T, Kollmann K, Braulke T, Reinheckel T, Dierks T, Damme M., J Biol Chem 289(40), 2014
PMID: 25135642
Transport of the GlcNAc-1-phosphotransferase α/β-subunit precursor protein to the Golgi apparatus requires a combinatorial sorting motif.
Franke M, Braulke T, Storch S., J Biol Chem 288(2), 2013
PMID: 23192343
Mass spectrometric analysis of neutral and anionic N-glycans from a Dictyostelium discoideum model for human congenital disorder of glycosylation CDG IL.
Hykollari A, Balog CI, Rendić D, Braulke T, Wilson IB, Paschinger K., J Proteome Res 12(3), 2013
PMID: 23320427
Synthesis of novel bivalent mimetic ligands for mannose-6-phosphate receptors.
Liu Y, Marshall J, Li Q, Edwards N, Chen G., Bioorg Med Chem Lett 23(8), 2013
PMID: 23473680
Ultrastructural analysis of neuronal and non-neuronal lysosomal storage in mucolipidosis type II knock-in mice.
Schweizer M, Markmann S, Braulke T, Kollmann K., Ultrastruct Pathol 37(5), 2013
PMID: 24047352
Decreased bone formation and increased osteoclastogenesis cause bone loss in mucolipidosis II.
Kollmann K, Pestka JM, Kühn SC, Schöne E, Schweizer M, Karkmann K, Otomo T, Catala-Lehnen P, Failla AV, Marshall RP, Krause M, Santer R, Amling M, Braulke T, Schinke T., EMBO Mol Med 5(12), 2013
PMID: 24127423
Excessive activity of cathepsin K is associated with cartilage defects in a zebrafish model of mucolipidosis II.
Petrey AC, Flanagan-Steet H, Johnson S, Fan X, De la Rosa M, Haskins ME, Nairn AV, Moremen KW, Steet R., Dis Model Mech 5(2), 2012
PMID: 22046029
The C proteins of human parainfluenza virus type 1 block IFN signaling by binding and retaining Stat1 in perinuclear aggregates at the late endosome.
Schomacker H, Hebner RM, Boonyaratanakornkit J, Surman S, Amaro-Carambot E, Collins PL, Schmidt AC., PLoS One 7(2), 2012
PMID: 22355301
Vertebrate protein glycosylation: diversity, synthesis and function.
Moremen KW, Tiemeyer M, Nairn AV., Nat Rev Mol Cell Biol 13(7), 2012
PMID: 22722607
Lysosomal dysfunction causes neurodegeneration in mucolipidosis II 'knock-in' mice.
Kollmann K, Damme M, Markmann S, Morelle W, Schweizer M, Hermans-Borgmeyer I, Röchert AK, Pohl S, Lübke T, Michalski JC, Käkelä R, Walkley SU, Braulke T., Brain 135(pt 9), 2012
PMID: 22961545
Autophagy and pancreatitis.
Gukovskaya AS, Gukovsky I., Am J Physiol Gastrointest Liver Physiol 303(9), 2012
PMID: 22961802
A case of mucolipidosis II presenting with prenatal skeletal dysplasia and severe secondary hyperparathyroidism at birth.
Heo JS, Choi KY, Sohn SH, Kim C, Kim YJ, Shin SH, Lee JM, Lee J, Sohn JA, Lim BC, Lee JA, Choi CW, Kim EK, Kim HS, Kim BI, Choi JH., Korean J Pediatr 55(11), 2012
PMID: 23227064
Newborn screening for lysosomal storage disorders.
Nakamura K, Hattori K, Endo F., Am J Med Genet C Semin Med Genet 157C(1), 2011
PMID: 21312327
Vacuolization of mucolipidosis type II mouse exocrine gland cells represents accumulation of autolysosomes.
Boonen M, van Meel E, Oorschot V, Klumperman J, Kornfeld S., Mol Biol Cell 22(8), 2011
PMID: 21325625
A key enzyme in the biogenesis of lysosomes is a protease that regulates cholesterol metabolism.
Marschner K, Kollmann K, Schweizer M, Braulke T, Pohl S., Science 333(6038), 2011
PMID: 21719679
Golgi glycosylation and human inherited diseases.
Freeze HH, Ng BG., Cold Spring Harb Perspect Biol 3(9), 2011
PMID: 21709180
Analysis of mannose 6-phosphate uncovering enzyme mutations associated with persistent stuttering.
Lee WS, Kang C, Drayna D, Kornfeld S., J Biol Chem 286(46), 2011
PMID: 21956109
Proteolytic processing of the gamma-subunit is associated with the failure to form GlcNAc-1-phosphotransferase complexes and mannose 6-phosphate residues on lysosomal enzymes in human macrophages.
Pohl S, Tiede S, Marschner K, Encarnação M, Castrichini M, Kollmann K, Muschol N, Ullrich K, Müller-Loennies S, Braulke T., J Biol Chem 285(31), 2010
PMID: 20489197
Pathology and current treatment of neurodegenerative sphingolipidoses.
Eckhardt M., Neuromolecular Med 12(4), 2010
PMID: 20730629
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