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Journal of Medicinal Chemistry|February 1, 2008
Synthesis and biological evaluation of NO-donor-tacrine hybrids as hepatoprotective anti-Alzheimer drug candidatesLei Fang, Dorothea Appenroth, Michael Decker, et al.Human Mutation|August 31, 2002
Analysis of the CTNS gene in patients of German and Swiss origin with nephropathic cystinosisMichael Kiehntopf, Jörg Schickel, Bärbel von der Gönne, et al.International Journal of Oncology|October 4, 2006
Outcome-based profiling of astrocytic tumours identifies prognostic gene expression signatures which link molecular and morphology-based pathologyChristian Beetz, Sven Bergner, Stefan Brodoehl, et al.Neurosurgical Review|March 3, 2007
A paediatric supratentorial primitive neuroectodermal tumour associated with malignant astrocytic transformation and a clonal origin of both componentsSusanne A Kuhn, Uwe-Karsten Hanisch, Kristian Ebmeier, et al.Human Mutation|January 31, 2014
Functional mutation analysis provides evidence for a role of REEP1 in lipid droplet biologyJulia Falk, Magdalena Rohde, Mohamed M Bekhite, et al.Journal of the Neurological Sciences|January 15, 2008
Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspotsChristian Beetz, Rebecca Schüle, Stephan Klebe, et al.Neurogenetics|October 16, 2008
Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegiaRebecca Schüle, Elisabeth Brandt, Kathrin N Karle, et al.Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|April 22, 2011
Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophreniaC Christoph Schultz, Igor Nenadic, Kathrin Koch, et al.Journal of Psychiatric Research|September 29, 2012
Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophreniaIgor Nenadic, Raka Maitra, Sigrid Scherpiet, et al.European Journal of Human Genetics : EJHG|September 27, 2007
A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large Brazilian pedigreeMiguel Mitne-Neto, Fernando Kok, Christian Beetz, et al.Pageof 5