Ralph Krätzner

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unigoe
 

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  • 2021 | Journal Article | Research Paper | 
    ​ ​LC-MS Based Platform Simplifies Access to Metabolomics for Peroxisomal Disorders​
    Klemp, H. G.; Kettwig, M.; Streit, F. ; Gärtner, J. ; Rosewich, H.   & Krätzner, R. ​ (2021) 
    Metabolites, 11(6) pp. 347​.​ DOI: https://doi.org/10.3390/metabo11060347 
    ​Details  DOI  PMID  PMC 
  • 2020 | Journal Article
    ​ ​tRNAArg-Derived Fragments Can Serve as Arginine Donors for Protein Arginylation​
    Avcilar-Kucukgoze, I.; Gamper, H.; Polte, C.; Ignatova, Z.; Kraetzner, R. ; Shtutman, M. & Hou, Y.-M. et al.​ (2020) 
    Cell Chemical Biology, 27(7) pp. 839​-849.e4​.​ DOI: https://doi.org/10.1016/j.chembiol.2020.05.013 
    ​Details  DOI 
  • 2017 | Journal Article
    ​ ​A new CUL4B variant associated with a mild phenotype and an exceptional pattern of leukoencephalopathy​
    Weissbach, S. ; Reinert, M.-C. ; Altmüller, J.; Krätzner, R. ; Thiele, H.; Rosenbaum, T. & Nürnberg, P. et al.​ (2017) 
    American Journal of Medical Genetics Part A, 173(10) pp. 2803​-2807​.​ DOI: https://doi.org/10.1002/ajmg.a.38390 
    ​Details  DOI 
  • 2014 | Journal Article | Research Paper | 
    ​ ​Structure of sulfamidase provides insight into the molecular pathology of mucopolysaccharidosis IIIA​
    Sidhu, N. S.; Schreiber, K.; Proepper, K.; Becker, S. ; Uson, I.; Sheldrick, G. M.   & Gärtner, J.  et al.​ (2014) 
    Acta Crystallographica Section D Biological Crystallography, 70 pp. 1321​-1335​.​ DOI: https://doi.org/10.1107/S1399004714002739 
    ​Details  DOI  PMID  PMC  WoS 
  • 2013 | Journal Article
    ​ ​A Novel SLC6A8 Mutation in a Large Family with X-Linked Intellectual Disability: Clinical and Proton Magnetic Resonance Spectroscopy Data of Both Hemizygous Males and Heterozygous Females​
    Dreha-Kulaczewski, S. ; Kalscheuer, V.; Tzschach, A.; Hu, H.; Helms, G.; Brockmann, K.   & Weddige, A.  et al.​ (2013) 
    JIMD reports, 13 pp. 91​-99​.​ DOI: https://doi.org/10.1007/8904_2013_261 
    ​Details  DOI  PMID  PMC 
  • 2012 | Journal Article | Research Paper | 
    ​ ​Structure and activity of the only human RNase T2​
    Thorn, A.; Steinfeld, R. ; Ziegenbein, M.; Grapp, M.; Hsiao, H.-H.; Urlaub, H.   & Sheldrick, G. M.  et al.​ (2012) 
    Nucleic Acids Research, 40(17) pp. 8733​-8742​.​ DOI: https://doi.org/10.1093/nar/gks614 
    ​Details  DOI  PMID  PMC  WoS 
  • 2011 | Journal Article
    ​ ​Lymphoblastoid cell lines for diagnosis of peroxisome biogenesis disorders​
    Grønborg, S.; Krätzner, R. ; Rosewich, H.   & Gärtner, J. ​ (2011) 
    JIMD reports, 1 pp. 29​-36​.​ DOI: https://doi.org/10.1007/8904_2011_12 
    ​Details  DOI  PMID  PMC 
  • 2010 | Journal Article | Research Paper
    ​ ​Typical cMRI Pattern as Diagnostic Clue for D-Bifunctional Protein Deficiency Without Apparent Biochemical Abnormalities in Plasma​
    Gronborg, S.; Kraetzner, R. ; Spiegler, J.; Ferdinandusse, S.; Wanders, R. J. A.; Waterham, H. R. & Gärtner, J. ​ (2010) 
    American Journal of Medical Genetics, 152A(11) pp. 2845​-2849​.​ DOI: https://doi.org/10.1002/ajmg.a.33677 
    ​Details  DOI  PMID  PMC  WoS 
  • 2009 | Journal Article | Research Paper
    ​ ​Structure of Tripeptidyl-peptidase I Provides Insight into the Molecular Basis of Late Infantile Neuronal Ceroid Lipofuscinosis​
    Pal, A.; Kraetzner, R. ; Gruene, T.; Grapp, M.; Schreiber, K.; Gronborg, M. & Urlaub, H.  et al.​ (2009) 
    Journal of biological chemistry, 284(6) pp. 3976​-3984​.​ DOI: https://doi.org/10.1074/jbc.M806947200 
    ​Details  DOI  PMID  PMC  WoS 
  • 2009 | Journal Article | Research Paper | 
    ​ ​RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection​
    Henneke, M.; Diekmann, S.; Ohlenbusch, A. ; Kaiser, J.; Engelbrecht, V.; Kohlschuetter, A. & Kraetzner, R.  et al.​ (2009) 
    Nature Genetics, 41(7) pp. 773​-775​.​ DOI: https://doi.org/10.1038/ng.398 
    ​Details  DOI  PMID  PMC  WoS 
  • 2007 | Journal Article | Research Paper
    ​ ​Laminin-alpha 4 and integrin-linked kinase mutations cause human cardiomyopathy via simultaneous defects in cardiomyocytes and endothelial cells​
    Knoell, R.; Postel, R.; Wang, J.; Kraetzner, R. ; Hennecke, G.; Vacaru, A. M. & Vakeel, P. et al.​ (2007) 
    Circulation, 116(5) pp. 515​-525​.​ DOI: https://doi.org/10.1161/CIRCULATIONAHA.107.689984 
    ​Details  DOI  PMID  PMC  WoS 
  • 2006 | Journal Article | Research Paper
    ​ ​Cathepsin D deficiency is associated with a human neurodegenerative disorder​
    Steinfeld, R. ; Reinhardt, K.; Schreiber, K.; Hillebrand, M.; Kraetzner, R. ; Brück, W.   & Saftig, P.  et al.​ (2006) 
    American journal of human genetics, 78(6) pp. 988​-998​.​ DOI: https://doi.org/10.1086/504159 
    ​Details  DOI  PMID  PMC  WoS 
  • 2000 | Journal Article
    ​ ​Metal alkoxides as versatile precursors for group 4 phosphonates: Synthesis and X-ray structure of a novel organosoluble zirconium phosphonate​
    Chakraborty, D.; Chandrasekhar, V.; Bhattacharjee, M.; Krätzner, R. ; Roesky, H. W. ; Noltemeyer, M. & Schmidt, H.-G.​ (2000) 
    Inorganic Chemistry, 39(1) pp. 23​-26​.​ DOI: https://doi.org/10.1021/ic9907361 
    ​Details  DOI  PMID  PMC  WoS 

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