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Medizinische Fakultät GRADUIERTENKOLLEG * "Biological basis of central nervous system diseases" * Sprecher: Prof. Dr. Georg Reiser |
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The Graduiertenkolleg 'Biological basis of central nervous system diseases'
is funded by the Deutsche Forschungsgemeinschaft as a graduate program
run by researchers from the University and the Leibniz Institute for Neurobiology.
It was founded in 1996 at the Medical Faculty of the Otto-von-Guericke
University in Magdeburg. An important part of its philosophy is an educational
program which is aimed to bridge the gap between clinical amd basic research
in the neurosciences. Moreover, the Kolleg provides excellent research
opportunities for young investigators at the postgraduate level with a
background and interest in biomedical research related to all aspects of
brain disorders. The broad spectrum of research topics is reflected in
an integrative research program combining state of the art technology with
interdisciplinary educational programs. The program leads to a Ph.D. or
M.D. degree and qualifies successful individuals for a carreer track in
all fields of brain research and moreover all aspects of life sciences.
Magdeburg has rapidly evolved to one of the neuroscience centers in
Germany in the last few years. Several groups have established a vigorous
research program which has attracted extramural funding and provides superb
research facilities. Apart from the Medical Faculty and the Leibniz Institute
for Neurobiology, researchers from the Departments of Pschology, Engeneering
and Chemistry contribute to Magdeburg`s interdisciplinary neuroscience
profile. As a consequence of these joint efforts the Otto-von-Guericke
University will establish in fall 1999 a new study program in neuroscience
leading to a Diploma or Master of Science degree.
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The Graduiertenkolleg "Biological Basis of Central Nervous System Diseases" funded by the Deutsche Forschungsgemeinschaft, is a graduate program at the Medical Faculty of the University of Magdeburg for PhD and MD students. We invite immediate applications for up to three years for
TOPICS: (Details see below)
MOLECULAR AND CELLULAR NEUROBIOLOGY:
Immunosuppressive mechanisms
following brain injury
"Synaptic tagging", LTP,
learning/memory
Ca2+ sources
in hypoxia-induced neuronal cell death
Microglial Ca2+
and Alzheimer beta-amyloid peptide
Opioid receptor and mechanisms
of opioid tolerance
Neuronal Ca2+
sensor proteins in apoptosis
Synaptic Ca2+
binding protein caldendrin
NEUROPHYSIOLOGY:
GABAergic thalamic mechanisms
in vitro (Postdoc)
Single cell activity in
learning animals
Chochlea implant and auditory
cortex stimulation
MEDICAL PSYCHOLOGY:
Computer-aided training
of patients with brain damage
Transition zones in visual
fields and event related potentials
NEUROHISTOLOGY AND ANATOMY:
Immunohistochemical studies
on human brain
Neurotrophin action and
rat hippocampus
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| Supervisor/
PI
Department |
PROJECT
Methods Aims |
| Prof. Dr. S. Ansorge
Institute of Experimental Internal Medicine Medical Faculty |
The role of alpha-MSH in neurotrauma induced
immunosuppression
Methods: ELISA, antibody generation, primary cultures of immune cells Aims: Focus of the study is a putative anti-inflammatory action of alpha-MSH on cytokine mediated secondary neurodegeneration in neurotrauma. |
| Prof. Dr. B. Bogerts
Clinic for Psychiatry, Psychotherapy and Psychosomatic Medicine Medical Faculty |
Hypothalamic peptides and nitric-oxid
synthase in human affective isorders
Methods: computer- assisted morphometry, immunocytochemistry Aims: The hypothesis that hyperthyreoism accompanies depressive disorders will be tested in human postmortem brain sections. |
| PD Dr. U. Frey
Department of Neurophysiology Leibniz Institute for Neurobiology |
"Synaptic tagging" in memory disorders
of the aged brain
Methods: in vivo and in vitro LTP, behavioral testing Aims: It is intended to clarify which impact the cholinergic innervation of the hippocampus has on "synaptic tagging" and LTP maintenance in young and senile rats. |
| Prof. Dr. E.D. Gundelfinger
Department of Neurochemistry / Molecular Biology Leibniz Institute for Neurobiology |
Involvement of neuronal calciumsensor
proteins in neurodegenerative diseases
Methods: cell culture, biochemical and molecular assays, immunocytochemistry, heterologous expression Aims: It will be investigated by which mechanisms neuronal calciumsensor proteins affect neuronal cell death and whether such mechanisms are involved in neurodegenerative diseases. |
| Prof. Dr. H.J. Heinze
Clinic for Neurophysiology Medical Faculty |
Restitution of attention performance in
brain damaged patients
Methods: computer-assisted training, EEG, MEG, fMRI Aims: Electrophysiological and metabolic correlates for the selection of perceptual information that will be stored in working memory will be identified. |
| Prof. Dr. V. Höllt
Institute for Pharmacology and Toxicology Medical Faculty |
Opioid receptor mutations in humans /
Molecular mechanisms of opioid tolerance
Methods: Molecular and biochemical assays, cell culture, animal models, heterologous expression systems Aims: The influence of polymorphisms in human opioid receptors on addictive behavior as well as the correlation between phosphorylation of opioid receptors and the development of opioid tolerance will be investigated. |
| Dr. M.R. Kreutz
Department of Neurochemistry / Molecular Biology, Leibniz Institute for Neurobiology |
Functional characterization of the neuronal
calcium-binding protein caldendrin
Methods: Molecular and biochemical assays, site specific mutagenesis, cell culture Aims: Genomic analysis of the caldendrin gene and analysis of protein-protein interactions of caldendrin will be performed. |
| Prof. Dr. H.C. Pape
Institute for Physiology Medical Faculty |
GABAergic mechanisms of thalamic absence
epilepsy
Methods: thalamic slice preparations, patch clamp, chloride-imaging Aims: The role fo GABAc receptors and somato-dendritic transmembrane chloride gradients the generation of thalamic epileptiform activity will be investigated. |
| Prof. Dr. G. Reiser
Institute for Neurobiochemistry Medical Faculty |
Modulation of Ca2+-homeostasis
by beta-amyloid protein in glial cells
Methods: primary cell culture, single cell Ca2+-imaging, Fura-2 fluorometry Aims: The function of immune cells in the brain is studied by testing whether beta-amyloid protein has a direct impact on intracellular calcium in microglia cells and cell survival. |
| Prof. Dr. K. Reymann
Leibniz Institute for Neurobiology / FAN-Institute |
Synaptinc plasticity in single neurons
of learning animals
Methods: single unit recording in freely moving rats during learning, induction of long-term potentiation (LTP) in limbic cortex; Aims: We investigate the correlation of LTP-capability of cortical neurons with their involvement in learning plasticity and different steps of food-reinforced operant behaviour. |
| Prof. Dr. B.A. Sabel
Institute for Medical Psychology Medical Faculty |
Determination of transition zones in patients
with visual deficits
Methods: Event-related potentials, perimetry, neuropsychological testing Aims: A diagnitic tool for the evaluation of visual transition zones on the basis of electrophsiological parameter will be developed. |
| Prof. Dr. H. Scheich /
Prof. Dr. H. von Specht Department of Acoustics, Learning and Language, Leibniz Institute for Neurobiology / Division of Experimental Audiology and Medical Physics Medical Faculty |
Cochlea implants and reorganization plasticity
in the auditory cortex
Methods: Evoked potentials, auditory discrimination learning, fMRI Aims: The studies optimize auditory stimulation patterns and language coding strategies in the auditory cortex on the search for cortical plasticity mechanisms in deafs. |
| Prof. Dr. H. Schwegler
Institute for Anatomy Medical Faculty |
Hormone and neurotrophin actions during
septal/hippocampal development
Methods: ELISA, RT-PCR, in situ hybridization, immunocytochemistry Aims: Experiments should evaluate the influence of corticosterone on cytoarchitecture and neurotrophin expression in the developing septo-hippocampal systems. |