Research Topics
Genomes and GenesSpecies | Ana Luisa PinaSummaryAffiliation: University of Regensburg Country: Germany Publications
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Detail Information
Publications
Expression of pigment-epithelium-derived factor during kidney development and agingAna Luisa Pina
Department of Neurosurgery, University Clinic of Regensburg, Franz Josef Strauss Allee 11, 93053, Regensburg, Germany
Cell Tissue Res 329:329-38. 2007....
Possible role of the C-reactive protein and white blood cell count in the pathogenesis of cerebral vasospasm following aneurysmal subarachnoid hemorrhageRalf Dirk Rothoerl
Department of Neurosurgery, University of Regensburg, Regensburg, Germany
J Neurosurg Anesthesiol 18:68-72. 2006....
Protein expression of pigment-epithelium-derived factor in rat cochleaOtto Gleich
Department of Otorhinolaryngology, University of Regensburg, Regensburg, Germany
Cell Tissue Res 332:565-71. 2008..Our data constitute the first report on the morphological protein distribution of this multifunctional molecule in the rat cochlea and suggest its role in important functions of the internal ear...
ICAM-1 and VCAM-1 expression following aneurysmal subarachnoid hemorrhage and their possible role in the pathophysiology of subsequent ischemic deficitsRalf Dirk Rothoerl
Department of Neurosurgery, University of Regensburg, Regensburg, Germany
Cerebrovasc Dis 22:143-9. 2006..There is growing evidence that inflammatory reactions could be involved in the pathogenesis of such delayed occurring ischemic lesions. The aim of this study was to evaluate adhesion molecules with regard to these lesions following SAH...
A missense mutation in GUCY2D acts as a genetic modifier in RPE65-related Leber Congenital AmaurosisEduardo Silva
Molecular and Developmental Biology Laboratory, Department of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
Ophthalmic Genet 25:205-17. 2004..We suggest that the unusual phenotypic variability in these two siblings with LCA is caused by the modifying effect of a heterozygous GUCY2D mutation observed against the disease background of a homozygous RPE65 mutation...
