Title: 2007
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Publikationen 2007

 

Baier, C., S. L. Baader, J. Jankowski, V. Gieselmann, K. Schilling, U. Rauch and J. Kappler (2007). "Hyaluronan is organized into fiber-like structures along migratory pathways in the developing mouse cerebellum." Matrix Biol 26(5): 348-58.Institut fur Physiologische Chemie, Rheinische Friedrich-Wilhelms-Universitat Bonn, Nussallee 11, D-53115 Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Becker, I., L. Wang-Eckhardt, A. Yaghootfam, V. Gieselmann and M. Eckhardt (2007). "Differential expression of (dihydro)ceramide synthases in mouse brain: oligodendrocyte-specific expression of CerS2/Lass2." Histochem Cell Biol.Institute of Physiological Chemistry, University of Bonn, 53115 , Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Benninger, Y., T. Thurnherr, J. A. Pereira, S. Krause, X. Wu, A. Chrostek-Grashoff, D. Herzog, K. A. Nave, R. J. Franklin, D. Meijer, C. Brakebusch, U. Suter and J. B. Relvas (2007). "Essential and distinct roles for cdc42 and rac1 in the regulation of Schwann cell biology during peripheral nervous system development." J Cell Biol 177(6): 1051-61.Institute of Cell Biology, Department of Biology, Eidgenossische Technische Hochschule Zurich, CH-8093 Zurich, Switzerland. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Bifsha, P., K. Landry, L. Ashmarina, S. Durand, V. Seyrantepe, S. Trudel, C. Quiniou, S. Chemtob, Y. Xu, R. A. Gravel, R. Sladek, A. V. Pshezhetsky (2007). Altered gene expression in cells from patients with lysosomal storage disorders suggests impairment of the ubiquitin pathway. Cell Death Differ 14(3): 511-23. Sainte-Justine Hospital, Department of Pediatrics and Biochemistry, University of Montreal, Montreal, Canada. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Brenk, C. H., E. C. Prott, D. Trost, A. Hoischen, C. Walldorf, B. Radlwimmer, D. Wieczorek, P. Propping, G. Gillessen-Kaesbach, R. G. Weber and H. Engels (2007). "Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation." Eur J Hum Genet 15(1): 35-44.Institut fur Humangenetik, Universitat Bonn, Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Brockmann, K., P. Dechent, C. Bonnemann, G. Schreiber, J. Frahm and F. Hanefeld (2007). "Quantitative proton MRS of cerebral metabolites in laminin alpha2 chain deficiency." Brain Dev 29(6): 357-64.Department of Paediatrics and Paediatric Neurology, Georg August University, 37075 Gottingen, Germany. kbrock@med.uni-goettingen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Farwanah, H., B. Pierstorff, C. E. Schmelzer, K. Raith, R. H. Neubert, T. Kolter, K. Sandhoff (2007). Separation and mass spectrometric characterization of covalently bound skin ceramides using LC/APCI-MS and Nano-ESI-MS/MS. J Chromatogr B Analyt Technol Biomed Life Sci. LIMES - Life and Medical Sciences Bonn, Program Unit Membrane and Lipid Biochemistry, Laboratory of Biology & Lipid Biochemistry, Friedrichs-Wilhelm-University, Gerhard-Domagk-Str. 1, D-53121 Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Dhaunchak, A. S. and K. A. Nave (2007). "A common mechanism of PLP/DM20 misfolding causes cysteine-mediated endoplasmic reticulum retention in oligodendrocytes and Pelizaeus Merzbacher disease." Proc Natl Acad Sci U S A 104(45): 17813-8.Department of Neurogenetics, Max Planck Institute of Experimental Medicine, D-37075 Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Ding, X. Q., O. Wittkugel, E. Goebell, A. F. Forster, U. Grzyska, H. Zeumer and J. Fiehler (2007). "Clinical applications of quantitative T2 determination: A complementary MRI tool for routine diagnosis of suspected myelination disorders." Eur J Paediatr Neurol.Department of Neuroradiology, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Eckhardt, M., K. K. Hedayati, J. Pitsch, R. Lullmann-Rauch, H. Beck, S. N. Fewou and V. Gieselmann (2007). "Sulfatide storage in neurons causes hyperexcitability and axonal degeneration in a mouse model of metachromatic leukodystrophy." J Neurosci 27(34): 9009-21.Institute of Physiological Chemistry, University of Bonn, 53115 Bonn, Germany. eckhardt@institut.physiochem.uni-bonn.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Ehrenreich, H., B. Fischer, C. Norra, F. Schellenberger, N. Stender, M. Stiefel, A. L. Siren, W. Paulus, K. A. Nave, R. Gold and C. Bartels (2007). "Exploring recombinant human erythropoietin in chronic progressive multiple sclerosis." Brain 130(Pt 10): 2577-88.Division of Clinical Neuroscience, Max Planck Institute of Experimental Medicine, Georg-August-University, Gottingen, Germany. ehrenreich@mpg.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Fewou, S. N., H. Ramakrishnan, H. Bussow, V. Gieselmann and M. Eckhardt (2007). "Down-regulation of polysialic acid is required for efficient myelin formation." J Biol Chem 282(22): 16700-11.Institute of Physiological Chemistry and Institute of Anatomy, University of Bonn, D-53115 Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Funfschilling, U., G. Saher, L. Xiao, W. Mobius, K. A. Nave (2007). Survival of adult neurons lacking cholesterol synthesis in vivo. BMC Neurosci 8: 1. Department of Neurogenetics, Max-Planck-Institute of Experimental Medicine, Hermann-Rein Strasse 3, D-37075 Gottingen, Germany. fuenfschilling@em.mpg.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Gareus, R., M. Huth, B. Breiden, A. Nenci, N. Rosch, I. Haase, W. Bloch, K. Sandhoff, M. Pasparakis (2007). Normal epidermal differentiation but impaired skin-barrier formation upon keratinocyte-restricted IKK1 ablation. Nat Cell Biol 9(4): 461-9. [1] Institute for Genetics, Department of Mouse Genetics and Inflammation, University of Cologne, Zulpicher Str. 47, 50674 Cologne, Germany. [2] EMBL Mouse Biology Unit, Via Ramarini 32, 00016 Monterotondo Scalo, Italy. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Gieselmann, V. (2007). "Sphingolipids in physiology and pathophysiology." Acta Paediatr Suppl 96(455): 39.Institute for Physiological Chemistry, Universitat Bonn, Bonn, Germany. gieselmann@institut.physiochem.uni-bonn.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Görg, M., W. Wilck, B. Granitzny, A. Suerken, Z. Lukacs, X. Ding, M. Schulte-Markwort, A. Kohlschütter (2007). Stabilization of Juvenile Metachromatic Leukodystrophy after Bone Marrow Transplantation: A 13 Year Follow-up. J Child Neurol in print. Departments of Pediatrics, Psychosomatics in Children and Adolescents, and Neuroradiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. kohlschuetter@uke.uni-hamburg.de

 

Groeschel, S., K. Brockmann, F. Hanefeld (2007). Virchow-Robin spaces on magnetic resonance images of children with adrenoleukodystrophy. Eur J Paediatr Neurol. Department of Pediatrics and Neuropediatrics, Georg-August-University, Goettingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Grove, M., N. H. Komiyama, K. A. Nave, S. G. Grant, D. L. Sherman, P. J. Brophy (2007). FAK is required for axonal sorting by Schwann cells. J Cell Biol 176(3): 277-82. Centre for Neuroscience Research, University of Edinburgh, Edinburgh EH9 1QH, Scotland, UK. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Guzzetta, A., M. Staudt, E. Petacchi, J. Ehlers, M. Erb, M. Wilke, I. Krageloh-Mann and G. Cioni (2007). "Brain representation of active and passive hand movements in children." Pediatr Res 61(4): 485-90.Department of Developmental Neuroscience, Stella Maris Scientific Institute, Pisa, Italy. a.guzzetta@inpe.unipi.it www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

He, Y., J. Dupree, J. Wang, J. Sandoval, J. Li, H. Liu, Y. Shi, K. A. Nave and P. Casaccia-Bonnefil (2007). "The transcription factor Yin Yang 1 is essential for oligodendrocyte progenitor differentiation." Neuron 55(2): 217-30.Department of Neuroscience and Cell Biology, R. Wood Johnson Medical School, Piscataway, NJ 08854, USA. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Hillebrand, M., S. E. Verrier, A. Ohlenbusch, A. Schafer, H. D. Soling, F. S. Wouters and J. Gartner (2007). "Live cell FRET microscopy: homo- and heterodimerization of two human peroxisomal ABC transporters, the adrenoleukodystrophy protein (ALDP, ABCD1) and PMP70 (ABCD3)." J Biol Chem 282(37): 26997-7005.Department of Pediatrics and Pediatric Neurology, Georg August University, Faculty of Medicine, Robert-Koch-Strasse 40, 37075 Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Hoffrogge, R., S. Beyer, R. Hubner, S. Mikkat, E. Mix, C. Scharf, U. Schmitz, S. Pauleweit, M. Berth, I. Z. Zubrzycki, H. Christoph, J. Pahnke, O. Wolkenhauer, A. Uhrmacher, U. Volker and A. Rolfs (2007). "2-DE profiling of GDNF overexpression-related proteome changes in differentiating ST14A rat progenitor cells." Proteomics 7(1): 33-46.Department of Neurology, Medical Faculty, Neurobiological Laboratory, University of Rostock, Rostock, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Huppke, P., K. Kohler, K. Brockmann, G. M. Stettner and J. Gartner (2007). "Treatment of epilepsy in Rett syndrome." Eur J Paediatr Neurol 11(1): 10-6.Department of Pediatrics and Pediatric Neurology, Georg August University, Robert-Koch-Strasse 40, D-37075 Gottingen, Germany. phuppke@med.uni-goettingen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Huttner, H. B., G. Richter, M. Hildebrandt, I. Blumcke, T. Fritscher, W. Bruck, J. Gartner, F. Seifert, D. Staykov, M. J. Hilz, S. Schwab and J. Bardutzky (2007). "Acute onset of fatal vegetative symptoms: unusual presentation of adult Alexander disease." Eur J Neurol 14(11): 1251-5.Department of Neurology, University of Erlangen, Erlangen, Germany. hagen.huttner@uk-erlangen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Ip, C. W., A. Kroner, P. R. Crocker, K. A. Nave, R. Martini (2007). Sialoadhesin deficiency ameliorates myelin degeneration and axonopathic changes in the CNS of PLP overexpressing mice. Neurobiol Dis 25(1): 105-11. Department of Neurology, Section of Developmental Neurobiology, University of Wuerzburg, Josef-Schneider Str. 11, D-97080 Wuerzburg, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Jennemann, R., R. Sandhoff, L. Langbein, S. Kaden, U. Rothermel, H. Gallala, K. Sandhoff, H. Wiegandt, H. J. Grone (2007). Integrity and barrier function of the epidermis critically depend on glucosylceramide synthesis. J Biol Chem 282(5): 3083-94. Department of Cellular und Molecular Pathology, German Cancer Research Center, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany. r.jennemann@dkfz.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Kanae, Y., D. Endoh, O. Yamato, D. Hayashi, S. Matsunaga, H. Ogawa, Y. Maede, M. Hayashi (2007). Nonsense mutation of feline beta-hexosaminidase beta-subunit (HEXB) gene causing Sandhoff disease in a family of Japanese domestic cats. Res Vet Sci 82(1): 54-60. Department of Veterinary Radiology, School of Veterinary Medicine, Rakuno Gakuen University, Ebetsu 069-8501, Japan. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Karim, S. A., J. A. Barrie, M. C. McCulloch, P. Montague, J. M. Edgar, D. Kirkham, T. J. Anderson, K. A. Nave, I. R. Griffiths, M. McLaughlin (2007). PLP overexpression perturbs myelin protein composition and myelination in a mouse model of Pelizaeus-Merzbacher disease. Glia 55(4): 341-51. Applied Neurobiology Group, Institute of Comparative Medicine, University of Glasgow, Bearsden, Glasgow, Scotland. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Kassmann, C. M., C. Lappe-Siefke, M. Baes, B. Brugger, A. Mildner, H. B. Werner, O. Natt, T. Michaelis, M. Prinz, J. Frahm and K. A. Nave (2007). "Axonal loss and neuroinflammation caused by peroxisome-deficient oligodendrocytes." Nat Genet 39(8): 969-76.Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Hermann-Rein-Strasse 3, D-37075 Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Kohlschuetter, A. (2007). "Mastering the dilemma of rare diseases." Neuropediatrics 38(1): 1 www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Krone, B., D. Pohl, K. Rostasy, E. Kahler, E. Brunner, F. Oeffner, J. M. Grange, J. Gartner and F. Hanefeld (2007). "Common infectious agents in multiple sclerosis: a case control study in children." Mult Scler.Department of Virology, Georg August University Goettingen,Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Lamanna, W. C., I. Kalus, M. Padva, R. J. Baldwin, C. L. Merry, T. Dierks (2007). The heparanome-The enigma of encoding and decoding heparan sulfate sulfation. J Biotechnol 129(2): 290-307. Department of Chemistry, Biochemistry I, Bielefeld University, Universitatsstr. 25, 33615 Bielefeld, Germany; Department of Biochemistry II, University of Gottingen, Heinrich-Duker-Weg 12, 37073 Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Leder, C., N. Schwab, C. W. Ip, A. Kroner, K. A. Nave, K. Dornmair, R. Martini and H. Wiendl (2007). "Clonal expansions of pathogenic CD8+ effector cells in the CNS of myelin mutant mice." Mol Cell Neurosci 36(3): 416-24.Department of Neurology, University of Wuerzburg, D-97080 Wuerzburg, Germany; Clinical Research Group for Multiple Sclerosis and Neuroimmunology, Department of Neurology, University of Wuerzburg, Josef-Schneider-Str. 11, 97080 Wuerzburg, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Lewerenz, J., X. Ding, J. Matschke, C. Schnabel, P. Emami, D. von Borczyskowski, R. Buchert, T. Krieger, M. de Wit, A. Munchau (2007). Dementia and leukoencephalopathy due to lymphomatosis cerebri. J Neurol Neurosurg Psychiatry. University Medical Center Hamburg-Eppendorf, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Matzner, U., F. Matthes, E. Herbst, R. Lullmann-Rauch, Z. Callaerts-Vegh, R. D'Hooge, C. Weigelt, C. Eistrup, J. Fogh and V. Gieselmann (2007). "Induction of tolerance to human arylsulfatase a in a mouse model of metachromatic leukodystrophy." Mol Med 13(9-10): 471-9.Institut fur Physiologische Chemie, Rheinische Friedrich-Wilhelms-Universitat, Nussallee 11, D-5315 Bonn, Germany. matzner@institut.physiochem.uni-bonn.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Mercimek-Mahmutoglu, S., S. Gruber, A. Rolfs, A. Stadlbauer, C. Woeber, P. Kurnik, T. Voigtlaender, E. Moser and S. Stoeckler-Ipsiroglu (2007). "Neurological and brain MRS findings in patients with Gaucher disease type 1." Mol Genet Metab 91(4): 390-5.Department of Pediatrics, Medical University Vienna, Austria. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Meyer, C., G. Schmid, S. Gorlitz, M. Ernst, C. Wilkens, I. Wilhelms, P. H. Kraus, P. Bauer, J. Tomiuk, H. Przuntek, A. Mugge and L. Schols (2007). "Cardiomyopathy in Friedreich's ataxia-assessment by cardiac MRI." Mov Disord 22(11): 1615-22.Department of Neurology, St. Josef Hospital, Ruhr-University Bochum, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Meyer zu Horste, G., T. Prukop, D. Liebetanz, W. Mobius, K. A. Nave, M. W. Sereda (2007). Antiprogesterone therapy uncouples axonal loss from demyelination in a transgenic rat model of CMT1A neuropathy. Ann Neurol 61(1): 61-72. Department of Neurogenetics, Max-Planck-Institute of Experimental Medicine, University of Gottingen, Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Nave, K. A., M. W. Sereda and H. Ehrenreich (2007). "Mechanisms of disease: inherited demyelinating neuropathies--from basic to clinical research." Nat Clin Pract Neurol 3(8): 453-64.Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Gottingen, Germany. nave@em.mpg.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Pagenstecher, C., D. Gadzicki, D. Stienen, S. Uhlhaas, E. Mangold, N. Rahner, M. Arslan-Kirchner, P. Propping, W. Friedl and S. Aretz (2007). "A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification." J Mol Diagn 9(1): 122-6.Institute of Human Genetics, University of Bonn, Wilhelmstrasse 31, D-53111 Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Pavlova, M., W. Lutzenberger, A. N. Sokolov, N. Birbaumer and I. Krageloh-Mann (2007). "Oscillatory MEG response to human locomotion is modulated by periventricular lesions." Neuroimage 35(3): 1256-63.Department of Paediatric Neurology and Child Development, Children's Hospital, University of Tubingen Medical School, University of Tubingen, Tubingen, Germany. marina.pavlova@uni-tuebingen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Pavlova, M., A. Sokolov and I. Krageloh-Mann (2007). "Visual navigation in adolescents with early periventricular lesions: knowing where, but not getting there." Cereb Cortex 17(2): 363-9.Developmental Cognitive and Social Neuroscience Unit, Department of Paediatric Neurology and Child Development, Children's Hospital, University of Tubingen, Tubingen, Germany. marina.pavlova@uni-tuebingen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Platt, M. J., C. Cans, A. Johnson, G. Surman, M. Topp, M. G. Torrioli and I. Krageloh-Mann (2007). "Trends in cerebral palsy among infants of very low birthweight (<1500 g) or born prematurely (<32 weeks) in 16 European centres: a database study." Lancet 369(9555): 43-50.Division of Public Health, Whelan Building, University of Liverpool, Liverpool L69 3GB, UK. mjplatt@liv.ac.uk www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Pohlmann-Eden, B., U. Stephani, I. Krageloh-Mann, B. Schmitt, U. Brandl and M. Holtkamp (2007). "[Management of refractory status epilepticus from a neurologic and neuropediatric perspective.]." Nervenarzt 78(8): 871-82.Epilepsie-Zentrum Bethel, Evangelisches Krankenhaus Bielefeld, Bielefeld, Deutschland. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Rahner, N., N. Friedrichs, V. Steinke, S. Aretz, W. Friedl, R. Buettner, E. Mangold, P. Propping and C. Walldorf (2007). "Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome." J Pathol.Institute of Human Genetics, University of Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Ramakrishnan, H., K. K. Hedayati, R. Lullmann-Rauch, C. Wessig, S. N. Fewou, H. Maier, H. H. Goebel, V. Gieselmann and M. Eckhardt (2007). "Increasing sulfatide synthesis in myelin-forming cells of arylsulfatase A-deficient mice causes demyelination and neurological symptoms reminiscent of human metachromatic leukodystrophy." J Neurosci 27(35): 9482-90.Institute of Physiological Chemistry, Rheinische Friedrich-Wilhelms University of Bonn, 53115 Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Remmel N, Locatelli-Hoops S, Breiden B, Schwarzmann G, Sandhoff K (2007)

Saposin B mobilizes lipids from cholesterol-poor and bis(monoacylglycero)phosphate-rich membranes at acidic pH. Unglycosylated patient variant saposin B lacks lipid-extraction capacity. FEBS J. 2007 Jul;274(13):3405-20LIMES, Membrane Biology & Lipid Biochemistry Unit, c/o Kekulé-Institut für Organische Chemie und Biochemie, University of Bonn, Germany

 

Riecker, A., T. Nagele, M. Henneke and L. Schols (2007). "Late onset vanishing white matter disease." J Neurol 254(4): 544-5 www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Riess, O., U. Rub, A. Pastore, P. Bauer and L. Schols (2007). "SCA3: Neurological features, pathogenesis and animal models." Cerebellum: 1-13.Department of Medical Genetics, University of Tuebingen, Tuebingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Rohkamm, B., M. M. Reilly, H. Lochmuller, B. Schlotter-Weigel, N. Barisic, L. Schols, G. Nicholson, D. Pareyson, M. Laura, A. R. Janecke, G. Miltenberger-Miltenyi, E. John, C. Fischer, F. Grill, W. Wakeling, M. Davis, T. R. Pieber and M. Auer-Grumbach (2007). "Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome." J Neurol Sci 263(1-2): 100-6.Institute of Human Genetics, Medical University Graz, Austria; Department of Internal Medicine, Diabetes and Metabolism, Medical University Graz, Austria. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Rub, U., K. Seidel, I. Ozerden, K. Gierga, E. R. Brunt, L. Schols, R. A. de Vos, W. den Dunnen, C. Schultz, G. Auburger and T. Deller (2007). "Consistent affection of the central somatosensory system in spinocerebellar ataxia type 2 and type 3 and its significance for clinical symptoms and rehabilitative therapy." Brain Res Rev 53(2): 235-49.Department of Clinical Neuroanatomy, J W Goethe-University, Theodor-Stern-Kai 7, D-60590 Frankfurt/Main, Germany. u.rueb@em.uni-frankfurt.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Rubio-Aliaga I, Soewarto D, Wagner S, Klaften M, Fuchs H, Kalaydjiev S, Busch DH, Klempt M, Rathkolb B, Wolf E, Abe K, Zeiser S, Przemeck GK, Beckers J, de Angelis MH. 2007 Genetics, A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse. 175(3):1451-63, Institute of Experimental Genetics, GSF Research Center for Environment and Health, 85764 Neuherberg, Germany.

 

Rummel, A., T. Eichner, T. Weil, T. Karnath, A. Gutcaits, S. Mahrhold, K. Sandhoff, R. L. Proia, K. R. Acharya, H. Bigalke, T. Binz (2007). Identification of the protein receptor binding site of botulinum neurotoxins B and G proves the double-receptor concept. Proc Natl Acad Sci U S A 104(1): 359-64. Institut fur Biochemie, OE 4310, and Institut fur Toxikologie, OE 5340, Medizinische Hochschule Hannover, Carl-Neuberg-Strasse 1, 30625 Hannover, Germany. rummel.andreas@mh-hannover.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Sanchez-Albisua, I., S. Borell-Kost, U. A. Mau-Holzmann, P. Licht and I. Krageloh-Mann (2007). "Increased frequency of severe major anomalies in children conceived by intracytoplasmic sperm injection." Dev Med Child Neurol 49(2): 129-34.University Children's Hospital, Department of Medical Genetics, Tubingen, Germany. iciar.sanchez@med.uni-tuebingen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Saravanan, K., H. Bussow, N. Weiler, V. Gieselmann and S. Franken (2007). "A spontaneously immortalized Schwann cell line to study the molecular aspects of metachromatic leukodystrophy." J Neurosci Methods 161(2): 223-33.Institut fur Physiologische Chemie, Rheinische Friedrich-Wilhelms-Universitat, Nussallee 11, 53115 Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Scheper, G. C., T. van der Klok, R. J. van Andel, C. G. van Berkel, M. Sissler, J. Smet, T. I. Muravina, S. V. Serkov, G. Uziel, M. Bugiani, R. Schiffmann, I. Krageloh-Mann, J. A. Smeitink, C. Florentz, R. Van Coster, J. C. Pronk and M. S. van der Knaap (2007). "Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation." Nat Genet 39(4): 534-9.Department of Pediatrics and Child Neurology, Vrije University Medical Center, 1081 HV Amsterdam, The Netherlands. gc.scheper@vumc.nl www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Schiewek, R., M. Schellentrager, R. Monnikes, M. Lorenz, R. Giese, K. J. Brockmann, S. Gab, T. Benter and O. J. Schmitz (2007). "Ultrasensitive determination of polycyclic aromatic compounds with atmospheric-pressure laser ionization as an interface for GC/MS." Anal Chem 79(11): 4135-40.Division of Analytical Chemistry, University of Wuppertal, Gauss-Strasse 20, 42119 Wuppertal, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Schirmbeck, F., A. Georgi, J. Strohmaier, C. Schmael, C. Knorr, R. A. Jamra, J. Schumacher, T. Becker, N. Klopp, T. Illig, M. Wulf, M. Schwarz, W. Maier, P. Propping, S. Cichon, M. M. Nothen, T. G. Schulze and M. Rietschel (2007). "No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample." Psychiatr Genet 17(2): 127.Division of Genetic Epidemiology, Central Institute of Mental Health, Mannheim, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

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1LIMES Membrane Biology and Lipid Biochemistry Unit, University Bonn, c/o Kekulé-Institute, Gerhard-Domagk-Strasse 1, D-53121 Bonn, Germany

 

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