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Forschungsdatenbank PMU-SQQUID

Publikationen

Gewähltes Keyword: neuronal migration


LC-MS/MS identification of doublecortin as abundant beta cell-selective protein discharged by damaged beta cells in vitro.
Jiang, L; Brackeva, B; Stangé, G; Verhaeghen, K; Costa, O; Couillard-Després, S; Rotheneichner, P; Aigner, L; Van Schravendijk, C; Pipeleers, D; Ling, Z; Gorus, F; Martens, GA;
J Proteomics. 2013; 80:26-80
Originalarbeiten (Zeitschrift)
Midbrain-hindbrain malformations in patients with malformations of cortical development and epilepsy: a series of 220 patients.
Kuchukhidze, G; Koppelstaetter, F; Unterberger, I; Dobesberger, J; Walser, G; Höfler, J; Zamarian, L; Haberlandt, E; Rostasy, K; Ortler, M; Czech, T; Feucht, M; Bauer, G; Delazer, M; Felber, S; Trinka, E;
Epilepsy Res. 2013; 106(1-2): 181-190.
Originalarbeiten (Zeitschrift)
Congruence of vascular network remodeling and neuronal dispersion in the hippocampus of reelin-deficient mice.
Lindhorst, T; Kurz, H; Sibbe, M; Meseke, M; Förster, E;
Histochem Cell Biol. 2012; 137(5):62-39
Originalarbeiten (Zeitschrift)
Targeted transgene expression in neuronal precursors: watching young neurons in the old brain.
Couillard-Despres, S; Winner, B; Karl, C; Lindemann, G; Schmid, P; Aigner, R; Laemke, J; Bogdahn, U; Winkler, J; Bischofberger, J; Aigner, L;
Eur J Neurosci. 2006; 24(6): 153-145.
Originalarbeiten (Zeitschrift)
Neuronal precursor-specific activity of a human doublecortin regulatory sequence.
Karl, C; Couillard-Despres, S; Prang, P; Munding, M; Kilb, W; Brigadski, T; Plötz, S; Mages, W; Luhmann, H; Winkler, J; Bogdahn, U; Aigner, L;
J Neurochem. 2005; 92(2):264-282
Originalarbeiten (Zeitschrift)
Mitotic impairment by doublecortin is diminished by doublecortin mutations found in patients.
Couillard-Despres, S; Uyanik, G; Ploetz, S; Karl, C; Koch, H; Winkler, J; Aigner, L;
Neurogenetics. 2004; 5(2): 83-93.
Originalarbeiten (Zeitschrift)
Transient expression of doublecortin during adult neurogenesis.
Brown, JP; Couillard-Després, S; Cooper-Kuhn, CM; Winkler, J; Aigner, L; Kuhn, HG;
J Comp Neurol. 2003; 467(1): 1-10.
Originalarbeiten (Zeitschrift)
Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders.
Holzfeind, PJ; Grewal, PK; Reitsamer, HA; Kechvar, J; Lassmann, H; Hoeger, H; Hewitt, JE; Bittner, RE;
Hum Mol Genet. 2002; 11(21): 2673-2687.
Originalarbeiten (Zeitschrift)
Molecular mechanisms of neuronal migration disorders, quo vadis?
Couillard-Despres, S; Winkler, J; Uyanik, G; Aigner, L;
Curr Mol Med. 2001; 1(6): 677-688.
Übersichtsarbeiten
A case of Ohtahara syndrome with olivary-dentate dysplasia and agenesis of mamillary bodies.
Trinka, E; Rauscher, C; Nagler, M; Moroder, T; Ladurner, G; Irnberger, E; Sperl, W; Pilz, P;
EPILEPSIA. 2001; 42(7): 950-953.
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