Search Results - "Stöhr, H."

Pupillary response to percutaneous auricular vagus nerve stimulation in alcohol withdrawal syndrome: A pilot trial by Treiber, M.C., Grünberger, J., Vyssoki, B., Szeles, J.C., Kaniusas, E., Kampusch, S., Stöhr, H., Walter, H., Lesch, O.M., König, D., Kraus, C.

“…Autonomic symptoms in alcohol withdrawal syndrome (AWS) are associated with a sympathetic-driven imbalance of the autonomic nervous system. To restore…”
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A protease isolated from human plasma activating factor VII independent of tissue factor by Römisch, J, Feussner, A, Vermöhlen, S, Stöhr, H A

“…An activity detected in a prothrombin complex concentrate, termed 'thrombin-like' due to its amidolytic properties, was recently reported by another working…”
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Quantitation of the factor VII- and single-chain plasminogen activator-activating protease in plasmas of healthy subjects by Römisch, J, Feussner, A, Stöhr, H A

“…Plasma samples of 189 healthy subjects were investigated for antigen levels of the recently reported factor VII- and single-chain plasminogen…”
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The FVII activating protease cleaves single-chain plasminogen activators by Römisch, J, Vermöhlen, S, Feussner, A, Stöhr, H

“…A serine protease isolated from plasma sharing structural characteristics with a hepatocyte growth factor activator-like protease has been demonstrated…”
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cDNA Cloning, Genomic Structure, and Chromosomal Localization of Three Members of the Human Fatty Acid Desaturase Family by Marquardt, Andreas, Stöhr, Heidi, White, Karen, Weber, Bernhard H.F.

“…The insertion of double bonds into specific positions of fatty acids is achieved by the action of distinct desaturase enzymes. Here we report the cloning and…”
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A Comprehensive Survey of Sequence Variation in the ABCA4 ( ABCR) Gene in Stargardt Disease and Age-Related Macular Degeneration by Rivera, Andrea, White, Karen, Stöhr, Heidi, Steiner, Klaus, Hemmrich, Nadine, Grimm, Timo, Jurklies, Bernhard, Lorenz, Birgit, Scholl, Hendrik P.N., Apfelstedt-Sylla, Eckhart, Weber, Bernhard H.F.

“…Stargardt disease (STGD) is a common autosomal recessive maculopathy of early and young-adult onset and is caused by alterations in the gene encoding the…”
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Mutations in a Novel Gene, VMD2; Encoding a Protein of Unknown Properties Cause Juvenile-Onset Vitelliform Macular Dystrophy (Best's Disease) by Marquardt, Andreas, Stöhr, Heidi, Passmore, Lori A., Krämer, Franziska, Rivera, Andrea, Weber, Bernhard H. F.

“…Vitelliform macular dystrophy (Best's disease) is an autosomal dominant, early-onset form of macular degeneration in which the primary defect is thought to…”
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PSYCHOPHYSIOLOGICAL DIAGNOSTICS IN ALCOHOL DEPENDENCY: FOURIER ANALYSIS OF PUPILLARY OSCILLATIONS AND THE RECEPTOR TEST FOR DETERMINATION OF CHOLINERGIC DEFICIENCY by GRÜNBERGER, J., LINZMAYER, L., WALTER, H., STÖHR, H., SALETU-ZYHLARZ, G. M., GRÜNBERGER, M., LESCH, O. M.

“…Mnestic disturbances in alcoholics may be related to cholinergic deficiency as well as to central nervous system inactivation. After instillation of…”
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Cloning and characterization of the murine Vmd2 RFP-TM gene family by Krämer, F, Stöhr, H, Weber, B H F

“…Mutations in the human vitelliform macular dystrophy type 2 (VMD2) gene are known to cause autosomal dominant Best macular dystrophy (BMD), a degenerative…”
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Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy by Weber, Bernhard H. F, Vogt, Gudrun, Pruett, Ronald C, Stöhr, Heidi, Felbor, Ute

“…The hereditary macular dystrophies are progressive degenerations of the central retina and contribute significantly to irreversible visual loss in developed…”
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The influence of the graft length on the functional and morphological result after nerve grafting: an experimental study in rabbits by Koller, R., Rab, M., Todoroff, B.P., Neumayer, Ch, Haslik, W., Sto¨hr, H.G., Frey, M.

“…Clinical experience shows that the results after the use of long nerve grafts for reconstruction are sometimes poor. Nevertheless several authors have stressed…”
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(ATTT)n-tetranucleotide repeat polymorphism in the 5'-flanking region of the UGB gene by Stöhr, H, Weber, B H

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Factor VII and single-chain plasminogen activator-activating protease: activation and autoactivation of the proenzyme by Kannemeier, C, Feussner, A, Stöhr, H A, Weisse, J, Preissner, K T, Römisch, J

“…Structural and biological characteristics of a recently described plasma serine protease, which displayed factor VII as well as pro-urokinase-activating…”
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Mapping and genomic characterization of the gene encoding diacylglycerol kinase γ (DAGK3) : assessment of its role in dominant optic atrophy (OPA1) by STÖHR, H, KLEIN, J, GEHRIG, A, KOEHLER, M. R, JURKLIES, B, KELLNER, U, LEO-KOTTLER, B, SCHMID, M, WEBER, B. H. F

“…The family of diacylglycerol kinases (DAGKs) is known to play an important role in signal transduction linked to phospholipid turnover. In the fruitfly…”
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A novel gene encoding a putative transmembrane protein with two extracellular CUB domains and a low-density lipoprotein class A module: isolation of alternatively spliced isoforms in retina and brain by Stöhr, Heidi, Berger, Claudia, Fröhlich, Susanne, Weber, Bernhard H.F.

“…We report herein the cDNA cloning of a novel retina and brain specific gene from mouse and human encoding a putative transmembrane protein with an N-terminal…”
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The influence of the donor nerve on the function and morphology of a mimic muscle after cross innervation: an experimental study in rabbits by Nehrer-Tairych, Greta V., Rab, Matthias, Deutinger, Maria, Frey, Manfred, Kamolz, Lars, Stöhr, Hans G.

“…In the present study we used the scutuloauricularis muscle in the rabbit to investigate the functional and morphometric alterations in the mimic-muscle system…”
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High-resolution meiotic and physical mapping of the best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome II by WEBER, B. H. F, VOGT, G, STÖHR, H, SANDER, S, WALKER, D, JONES, C

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High-resolution meiotic and physical mapping of the best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome 11 by Weber, B H, Vogt, G, Stöhr, H, Sander, S, Walker, D, Jones, C

“…Best vitelliform macular dystrophy (VMD2) has previously been linked to several microsatellite markers from chromosome 11. Subsequently, additional genetic…”
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Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration by Sauer, Christian G, White, Karen, Stöhr, Heidi, Grimm, Tiemo, Hutchinson, Amy, Bernstein, Paul S, Lewis, Richard Allan, Simonelli, Francesca, Pauleikhoff, Daniel, Allikmets, Rando, Weber, Bernhard H F

“…BACKGROUND A long term project was initiated to identify and to characterise genes that are expressed exclusively or preferentially in the retina as candidates…”
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Inherited retinal or optic nerve disorders – five steps to diagnosis by Kellner, U, Kellner, S, Weinitz, S, Farmand, G, Weber, B H F, Stöhr, H

“…An early diagnosis of inherited retinal or optic nerve disorders is often delayed due to unspecific clinical signs, multiple clinical manifestations and…”
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