Author Schmidt, Bernhard
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1988 | Journal Article |
Human lysosomal acid phosphatase: cloning, expression and chromosomal assignment
Pohlmann, R.; Krentler, C.; Schmidt, B.; Schröder, W.; Lorkowski, G.; Culley, J. & Mersmann, G. et al. (1988)
The EMBO Journal, 7(8) pp. 2343-2350.
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1990 | Journal Article |
Targeting of a lysosomal membrane protein: a tyrosine-containing endocytosis signal in the cytoplasmic tail of lysosomal acid phosphatase is necessary and sufficient for targeting to lysosomes
Peters, C.; Braun, M.; Weber, B.; Wendland, M.; Schmidt, B.; Pohlmann, R. & Waheed, A. et al. (1990)
The EMBO Journal, 9(11) pp. 3497-3506.
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1992 | Journal Article |
The internalization signal in the cytoplasmic tail of lysosomal acid phosphatase consists of the hexapeptide PGYRHV
Lehmann, L. E.; Eberle, W.; Krull, S.; Prill, V.; Schmidt, B.; Sander, C. & Figura, K. von et al. (1992)
The EMBO Journal, 11(12) pp. 4391-4399.
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1995 | Journal Article |
A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency
Schmidt, B.; Selmer, T.; Ingendoh, A. & Figura, K. von (1995)
Cell, 82 pp. 271-278.
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1996 | Journal Article |
Guanidinoacetate methyltransferase deficiency: the first inborn error of creatine metabolism in man
Stockler, S.; Isbrandt, D.; Hanefeld, F.; Schmidt, B. & Figura, K. von (1996)
American Journal of Human Genetics, 58 pp. 914-922.
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1999 | Journal Article |
Sequence determinants directing conversion of cysteine to formylglycine in eukaryotic sulfatases
Dierks, T.; Lecca, M.; Schlotterhose, P.; Schmidt, B. & Figura, K. von (1999)
The EMBO Journal, 18(8) pp. 2084-2091.
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2003 | Journal Article |
Multiple sulfatase deficiency is caused by mutations in the gene encoding the human Cα-Formylglycine generating enzyme
Dierks, T.; Schmidt, B.; Borissenko, L. V.; Peng, J.; Preusser, A.; Mariappan, M. & Figura, K. von (2003)
Cell, 113 pp. 435-444.
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2005 | Journal Article
The Rat Expresses Two Complement Factor C4 Proteins, but Only One Isotype Is Expressed in the Liver
Roos, C.; Dressel, R.; Schmidt, B.; Günther, E. & Walter, L. (2005)
The Journal of Immunology, 174(2) pp. 970-975. DOI: https://doi.org/10.4049/jimmunol.174.2.970
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2007 | Journal Article
Characterisation of lipofuscin-like lysosomal inclusion bodies from human placenta
Schroeder, B.; Elsaesser, H.-P.; Schmidt, B. & Hasilik, A. (2007)
FEBS Letters, 581(1) pp. 102-108. DOI: https://doi.org/10.1016/j.febslet.2006.12.005
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2007 | Journal Article
Probing the oxygen-binding site of the human formylglycine-generating enzyme using halide ions
Roeser, D.; Schmidt, B.; Preusser-Kunze, A. & Rudolph, M. G. (2007)
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 63 pp. 621-627. DOI: https://doi.org/10.1107/S0907444907009961
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2008 | Journal Article
ERp44 mediates a thiol-independent retention of formylglycine-generating enzyme in the endoplasmic reticulum
Mariappan, M.; Radhakrishnan, K.; Dierks, T.; Schmidt, B. & von Figura, K. (2008)
Journal of Biological Chemistry, 283(10) pp. 6375-6383. DOI: https://doi.org/10.1074/jbc.M709171200
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2008 | Journal Article
The non-catalytic N-terminal extension of formylglycine-generating enzyme is required for its biological activity and retention in the endoplasmic reticulum
Mariappan, M.; Gande, S. L.; Radhakrishnan, K.; Schmidt, B.; Dierks, T. & von Figura, K. (2008)
Journal of Biological Chemistry, 283(17) pp. 11556-11564. DOI: https://doi.org/10.1074/jbc.M707858200
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2008 | Journal Article
Paralog of the formylglycine-generating enzyme - retention in the endoplasmic reticulum by canonical and noncanonical signals
Gande, S. L.; Mariappan, M.; Schmidt, B.; Pringle, T. H.; von Figura, K. & Dierks, T. (2008)
FEBS Journal, 275(6) pp. 1118-1130. DOI: https://doi.org/10.1111/j.1742-4658.2008.06271.x
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2009 | Journal Article
M Phase-Specific Phosphorylation of Histone H1.5 at Threonine 10 by GSK-3
Happel, N.; Stoldt, S.; Schmidt, B. & Doenecke, D. (2009)
Journal of Molecular Biology, 386(2) pp. 339-350. DOI: https://doi.org/10.1016/j.jmb.2008.12.047
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2009 | Review
Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann-Pick C1 disease - Lysosomal storage disorders caused by defects of non-lysosomal proteins
Dierks, T.; Schlotawa, L.; Frese, M.-A.; Radhakrishnan, K.; von Figura, K. & Schmidt, B. (2009)
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1793(4) pp. 710-725.
Elsevier Science Bv. DOI: https://doi.org/10.1016/j.bbamcr.2008.11.015
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2009 | Journal Article
NCU-G1 is a highly glycosylated integral membrane protein of the lysosome
Schieweck, O.; Damme, M.; Schroeder, B.; Hasilik, A.; Schmidt, B. & Luebke, T. (2009)
Biochemical Journal, 422 pp. 83-90. DOI: https://doi.org/10.1042/BJ20090567
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2010 | Journal Article
Impaired Lysosomal Trimming of N-Linked Oligosaccharides Leads to Hyperglycosylation of Native Lysosomal Proteins in Mice with alpha-Mannosidosis
Damme, M.; Morelle, W.; Schmidt, B.; Andersson, C.; Fogh, J.; Michalski, J.-C. & Luebke, T. (2010)
Molecular and Cellular Biology, 30(1) pp. 273-283. DOI: https://doi.org/10.1128/MCB.01143-09
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2012 | Conference Abstract
Calcium and redox dependent conformational change is necessary for the catalytic activity of Formylglycine-Generating Enzyme (FGE): Insights into the mechanism of formylglycine generation
Alam, M. S.; Radhakrishnan, K. & Schmidt, B. (2012)
Protein Science, 21 26th Annual Symposium of the Protein-Society, San Diego, CA.
Hoboken: Wiley-blackwell.
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2012 | Journal Article
Mannose 6 Dephosphorylation of Lysosomal Proteins Mediated by Acid Phosphatases Acp2 and Acp5
Makrypidi, G.; Damme, M.; Mueller-Loennies, S.; Trusch, M.; Schmidt, B.; Schlueter, H. & Heeren, J. et al. (2012)
Molecular and Cellular Biology, 32(4) pp. 774-782. DOI: https://doi.org/10.1128/MCB.06195-11
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2013 | Journal Article | Research Paper
Mass spectrometry imaging: linking molecule profiles to tissue spatial distribution
Dihazi, H.; Bohrer, R.; Jahn, O.; Lenz, C.; Majcherczyk, A.; Schmidt, B. & Urlaub, H. et al. (2013)
Expert Review of Proteomics, 10(1) pp. 17-20. DOI: https://doi.org/10.1586/epr.12.73
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