His scientific interests lie mostly in Molecular biology, Biochemistry, Cell biology, Gene and Glycogen phosphorylase. The Molecular biology study combines topics in areas such as Synapsin I, Protein subunit, Phosphorylase kinase, Protein kinase A and 5' flanking region. His work on Complementary DNA, Protein primary structure, Peptide sequence and Gene expression as part of general Biochemistry study is frequently linked to Creatine transport, bridging the gap between disciplines.
His studies deal with areas such as Intracellular vesicle, Active zone and MARCKS as well as Cell biology. Manfred W. Kilimann combines subjects such as Paralemmin and Endocrinology with his study of Gene. His Glycogen phosphorylase research integrates issues from Mutation, Glycogen storage disease and G alpha subunit.
Manfred W. Kilimann mainly investigates Phosphorylase kinase, Molecular biology, Cell biology, Biochemistry and Genetics. His Phosphorylase kinase research is multidisciplinary, relying on both Mutation and Gene isoform. His Mutation research includes themes of Glycogen storage disease and Glycogen Storage Disease Type IX.
His research integrates issues of Synapsin I, Protein kinase A, G alpha subunit, RNA splicing and Exon in his study of Molecular biology. His work on Signal transducing adaptor protein as part of general Cell biology research is often related to Amphiphysin, thus linking different fields of science. His research in Point mutation intersects with topics in Endocrinology and Internal medicine.
The scientist’s investigation covers issues in Cell biology, LRBA, Paralemmin, Signal transducing adaptor protein and Neurotransmission. His work in the fields of Cilium overlaps with other areas such as Lymphangiogenesis. His LRBA research includes elements of Bioinformatics, Receptor potential, Protein domain and Vomeronasal organ, Sensory system.
His Paralemmin study incorporates themes from Lymph node stromal cell, Angiogenesis and Lymphatic Endothelium. He interconnects Synaptic plasticity and Cytoskeleton in the investigation of issues within Neurotransmission. His Synaptic plasticity research also works with subjects such as
His primary scientific interests are in Cell biology, Neurotransmission, Neurotransmitter receptor, Vacuolar protein sorting and Immunogold labelling. His work on Synaptogenesis as part of general Cell biology study is frequently linked to Synaptopodin, therefore connecting diverse disciplines of science. His research in the fields of Postsynaptic density overlaps with other disciplines such as Ion channel linked receptors, Kainate receptor and Silent synapse.
Manfred W. Kilimann performs multidisciplinary study in the fields of Neurotransmitter receptor and Long-term depression via his papers. His Vacuolar protein sorting study integrates concerns from other disciplines, such as VPS35 and Inhibitory postsynaptic potential. His Immunogold labelling research covers fields of interest such as Cytoskeleton, Exocytosis, Ribbon, Neurotransmitter and Ribbon synapse.
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A Na(+)-dependent creatine transporter in rabbit brain, muscle, heart, and kidney. cDNA cloning and functional expression.
C. Guimbal;M.W. Kilimann.
Journal of Biological Chemistry (1993)
Amphiphysin autoimmunity: Paraneoplastic accompaniments
Sean J. Pittock;Claudia F. Lucchinetti;Joseph E. Parisi;Eduardo E. Benarroch.
Annals of Neurology (2005)
Complete rescue of obesity, diabetes, and infertility in db/db mice by neuron-specific LEPR-B transgenes
Carl De Luca;Timothy J. Kowalski;Yiying Zhang;Joel K. Elmquist.
Journal of Clinical Investigation (2005)
Aczonin, a 550-Kd Putative Scaffolding Protein of Presynaptic Active Zones, Shares Homology Regions with Rim and Bassoon and Binds Profilin
Xiaolu Wang;Mark Kibschull;Michael M. Laue;Beate Lichte.
Journal of Cell Biology (1999)
Amphiphysin, a novel protein associated with synaptic vesicles.
B Lichte;R W Veh;H E Meyer;M W Kilimann.
The EMBO Journal (1992)
Neurobeachin: A Protein Kinase A-Anchoring,beige/Chediak-Higashi Protein Homolog Implicated in Neuronal Membrane Traffic
Xiaolu Wang;Friedrich W. Herberg;Michael M. Laue;Christiane Wüllner.
The Journal of Neuroscience (2000)
Unequal homologous recombination between LINE-1 elements as a mutational mechanism in human genetic disease.
Barbara Burwinkel;Manfred W. Kilimann.
Journal of Molecular Biology (1998)
Fatal Congenital Heart Glycogenosis Caused by a Recurrent Activating R531Q Mutation in the γ2-Subunit of AMP-Activated Protein Kinase (PRKAG2), Not by Phosphorylase Kinase Deficiency
Barbara Burwinkel;John W. Scott;Christoph Bührer;Frank K.H. van Landeghem.
American Journal of Human Genetics (2005)
The 5'-flanking region of the synapsin I gene. A G+C-rich, TATA- and CAAT-less, phylogenetically conserved sequence with cell type-specific promoter function.
A Sauerwald;C Hoesche;R Oschwald;M W Kilimann.
Journal of Biological Chemistry (1990)
The 5'-flanking region of the rat synapsin I gene directs neuron-specific and developmentally regulated reporter gene expression in transgenic mice.
C Hoesche;A Sauerwald;R W Veh;B Krippl.
Journal of Biological Chemistry (1993)
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