Author Schlotawa, Lars

• 2001 | Journal Article
  ​ ​Protein kinase C-independent stimulation of activator protein-1 and c-Jun N-terminal kinase activity in human endometrial cancer cells by the LHRH agonist triptorelin​
  Grundker, C. ; Schlotawa, L.; Viereck, V. & Emons, G.​ (2001) 
  European Journal of Endocrinology, 145(5) pp. 651​-658​.​ DOI: https://doi.org/10.1530/eje.0.1450651 
  ​Details  DOI  PMID  PMC  WoS 

• 2004 | Journal Article
  ​ ​Antiproliferative effects of the GnRH antagonist cetrorelix and of GnRH-II on human endometrial and ovarian cancer cells are not mediated through the GnRH type I receptor​
  Grundker, C.; Schlotawa, L.; Viereck, V.; Eicke, N.; Horst, A.; Kairies, B. & Emons, G.​ (2004) 
  European Journal of Endocrinology, 151(1) pp. 141​-149​.​ DOI: https://doi.org/10.1530/eje.0.1510141 
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• 2007 | Conference Abstract
  ​ ​Molecular and clinical characterization of multiple suleatase deficiency causing mutations in the formylglycine-generating enzyme​
  Schlotawa, L.; Steinfeld, R.; von Figura, K.; Dierks, T. & Gaertner, J. ​ (2007)
  Journal of Inherited Metabolic Disease, 30 
  Dordrecht​: Springer.
  ​Details  WoS 

• 2008 | Conference Abstract
  ​ ​Disease severity in multiple suleatase deficiency is determined by stability and residual activity of mutant formyl-glycine-generating enzyme​
  Schlotawa, L.; Dierks, T.; Schmidt, B. & Gaertner, J. ​ (2008)
  Journal of Inherited Metabolic Disease, 31 
  Dordrecht​: Springer.
  ​Details  WoS 

• 2008 | Journal Article
  ​ ​Increase of doxorubicin-induced apoptosis after knock-down of gonadotropin-releasing hormone receptor expression in human endometrial, ovarian and breast cancer cells​
  Fister, S.; Schlotawa, L.; Gunthert, A. R.; Emons, G.   & Gründker, C. ​ (2008) 
  Gynecological Endocrinology, 24(1) pp. 24​-29​.​ DOI: https://doi.org/10.1080/09513590701668882 
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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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• 2010 | Conference Abstract
  ​ ​FUNCTIONAL CHARACTERIZATION OF TWO NOVEL SUMF1 MUTATIONS LEADING TO A MILD PHENOTYPE IN MULTIPLE SULFATASE DEFICIENCY​
  Schlotawa, L.; Radhakrishnan, K.; Schmid, R.; Schmidt, B. ; Dierks, T.; Gaertner, J.   & Baumgartner, M.​ (2010)
  Journal of Inherited Metabolic Disease, 33 
  Dordrecht​: Springer.
  ​Details  WoS 

• 2011 | Journal Article | Research Paper | 
  ​ ​SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency​
  Schlotawa, L.; Ennemann, E. C.; Radhakrishnan, K.; Schmidt, B. ; Chakrapani, A.; Christen, H.-J. & Moser, H. et al.​ (2011) 
  European Journal of Human Genetics, 19(3) pp. 253​-261​.​ DOI: https://doi.org/10.1038/ejhg.2010.219 
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• 2013 | Journal Article | Research Paper | 
  ​ ​Rapid degradation of an active formylglycine generating enzyme variant leads to a late infantile severe form of multiple sulfatase deficiency​
  Schlotawa, L.; Radhakrishnan, K.; Baumgartner, M.; Schmid, R.; Schmidt, B. ; Dierks, T. & Gärtner, J. ​ (2013) 
  European Journal of Human Genetics, 21(9) pp. 1020​-1023​.​ DOI: https://doi.org/10.1038/ejhg.2012.291 
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• 2013 | Journal Article | Letter Note
  ​ ​Cerebellar ataxia, mental retardation and dysequilibrium syndrome 1 (CAMRQ1) caused by an unusual constellation of VLDLR mutation​
  Schlotawa, L.; Hotz, A.; Zeschnigk, C.; Hartmann, B.; Gärtner, J.   & Morris-Rosendahl, D.​ (2013) 
  Journal of Neurology, 260(6) pp. 1678​-1680​.​ DOI: https://doi.org/10.1007/s00415-013-6941-z 
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