Senn, Oliver, Russi, Erich W, Schindler, Christian, Imboden, Medea, Von Eckardstein, Arnold, Brändli, Otto, ...
Abstract Background Severe alpha1-antitrypsin (AAT) deficiency associated with low AAT blood concentrations is an established genetic COPD risk factor. Less is known about the respiratory health...
Imboden, Medea, Downs, Sara H, Senn, Oliver, Matyas, Gabor, Brändli, Otto, Russi, Erich W, ...
Abstract Background Understanding the environmental and genetic risk factors of accelerated lung function decline in the general population is a first step in a prevention strategy against the...
Minnie Hsieh, Derek Boerboom, Masayuki Shimada, Yuet Lo, Albert F. Parlow, ...
Previous studies showed that transcripts encoding specific Wnt ligands and Frizzled receptors including Wnt4, Frizzled1 (Fzd1), and Frizzled4 (Fzd4) were expressed in a cell-specific manner in the...
Preface, in The Nordic Seas: An Integrated perspective (2005)
Drange, Helge, Dokken, Trond M., Furevik, Tore, Gerdes, Rüdiger, Berger, Wolfgang
Preface
Die vorliegende pharmakopsychologische Studie wurde als explorative Kontrolluntersuchung zur Studie Influence of Valerian Treatment on Reaction Time, Alertness and Concentration in Volunteers...
Zeitz,Christina, Scherthan,Harry, Freier,Susanne, Feil,Silke, Suckow,Vanessa, Schweiger,Susann, ...
PURPOSE. The complete type of X-linked congenital stationary night blindness (CSNB1) in human and mouse is caused by mutations in the NYX gene. The human NYX protein has been predicted to contain an...
Isolation of the mouse nyctalopin gene Nyx and expression studies in mouse and rat retina (2003)
Pesch,Katrin, Zeitz,Christina, Fries,Julia E., Muenscher,Stefanie, Pusch,Carsten M., Kohler,Konrad, ...
PURPOSE: It has been shown recently that mutations in NYX (nyctalopin on chromosome X), encoding a novel protein associated with the leucine-rich repeat (LRR) protein superfamily, are responsible for...
Zeitz, Christina, Scherthan, Harry, Freier, Susanne, Feil, Silke, Suckow, Vanessa, Schweiger, Susann, ...
PURPOSE. The complete type of X-linked congenital stationary night blindness (CSNB1) in human and mouse is caused by mutations in the NYX gene. The human NYX protein has been predicted to contain an...
Isolation of the mouse nyctalopin gene Nyx and expression studies in mouse and rat retina (2003)
Pesch, Katrin, Zeitz, Christina, Fries, Julia E., Muenscher, Stefanie, Pusch, Carsten M., Kohler, Konrad, ...
PURPOSE: It has been shown recently that mutations in NYX (nyctalopin on chromosome X), encoding a novel protein associated with the leucine-rich repeat (LRR) protein superfamily, are responsible for...
Lenzner,Steffen, Prietz,Sandra, Feil,Silke, Nuber,Ulrike A., Ropers,Hans Hilger, Berger,Wolfgang
PURPOSE. Mutations in the NDP gene give rise to a variety of eye diseases, including classic Norrie disease (ND), X-linked exudative vitreoretinopathy (EVRX), retinal telangiectasis (Coats disease),...
Vascular Defects and Sensorineural Deafness in a Mouse Model of Norrie Disease (2002)
Rehm,Heidi L., Zhang,Duan-Sun, Brown,M. Christian, Burgess,Barbara, Halpin,Chris, Berger,Wolfgang, ...
Norrie disease is an X-linked recessive syndrome of blindness, deafness, and mental retardation. A knock-out mouse model with an Ndp gene disruption was studied. We examined the hearing phenotype,...
Lenzner, Steffen, Prietz, Sandra, Feil, Silke, Nuber, Ulrike A., Ropers, Hans Hilger, Berger, Wolfgang
PURPOSE. Mutations in the NDP gene give rise to a variety of eye diseases, including classic Norrie disease (ND), X-linked exudative vitreoretinopathy (EVRX), retinal telangiectasis (Coats disease),...
Vascular Defects and Sensorineural Deafness in a Mouse Model of Norrie Disease (2002)
Rehm, Heidi L., Zhang, Duan-Sun, Brown, M. Christian, Burgess, Barbara, Halpin, Chris, Berger, Wolfgang, ...
Norrie disease is an X-linked recessive syndrome of blindness, deafness, and mental retardation. A knock-out mouse model with an Ndp gene disruption was studied. We examined the hearing phenotype,...
Sudbrak, Ralf, Wieczorek, Georg, Nuber, Ulrike A., Mann, Wolfgang, Kirchner, Roland, Erdogan, Fikret, ...
Mutant alleles are frequently characterized by low expression levels. Therefore, cDNA array-based gene expression profiling may be a promising strategy for identifying gene defects underlying...
Mutations in the X-linked RP2 gene cause intracellular misrouting and loss of the protein (2001)
Schwahn, Uwe, Paland, Nicole, Techritz, Sandra, Lenzner, Steffen, Berger, Wolfgang
Mutations in RP2 cause the second most frequent form of X-linked retinitis pigmentosa, a severe retinal degeneration that leads to loss of visual acuity and blindness. The RP2 gene encodes a protein...
München, Universiẗat der Bundeswehr, Diss., 2000.
Roepman, Ronald, Bernoud-Hubac, Nathalie, Schick, Diana E., Maugeri, Alessandra, Berger, Wolfgang, Ropers, Hans-Hilger, ...
Mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene cause X-linked retinitis pigmentosa type 3 (RP3), a severe, progressive and degenerative retinal dystrophy eventually leading to...
The goal of the study is to produce a reliable working life assessment for construction components made out of metal-matrix compounds with complex micro structures. In addition, the results should...
Aufklärung von Gendefekten hereditärer Augenerkrankungen / (1998)
Beitr. teilw. dt., teilw. engl. - Enth. 16 Sonderabdr. aus verschiedenen Zeitschr.
Mutations in the candidate gene for Norrie disease (1992)
Berger, Wolfgang, De Pol, Dorien Van, Warburg, Mette, Gal, Andreas, Bleeker-Wagemakers, Liesbeth, De Silva, Harendra, ...
Recently, we and others have isolated a candidate gene for X linked Norrie disease (ND) which was found to be deleted or disrupted in several patients. As a prerequisite for the identification of...
Berlin, Humboldt-Univ., Diss. A, 1989 (Nicht f.d. Austausch).
Der Akute rechte Unterbauch differentialdiagnostische Schwierigkeiten / (1987)
Thesis (doctoral)--Rheinische Friedrich-Wilhelms-Universität zu Bonn, 1987.
Hyperkoagulabilität bei bösartigen Neubildungen unter zytostatischer Polychemotherapie / (1985)
Thesis (doctoral)--Ludwig-Maximilians Universität München, 1985.
Thesis (doctoral)--Technische Universität München, 1984.
Die Beschreibung der Proposition bei der Analyse englischer Texte. (1984)
Leipzig, Univ., Diss. A, 1984 (Nicht f.d. Austausch).
Zur Metallogenie der zinn-wolframführenden Struktur Sachsenhöhe/Osterzgebirge / (1983)
Greifswald, Univ., Diss. A, 1984 (Nicht für den Austausch).
Karl-Marx-Stadt, Techn. Hochsch., Diss. A, 1982 (Nicht für den Austausch).
Thesis (doctoral)--Albert-Ludwigs-Universität zu Freiburg i. Breisgau, 1978.
Entwurf und Untersuchung einer nicht-klassischen Logik für logische Falschheit / (1977)
Proefschrift Stuttgart.
Berlin, Humboldt-Univ., Biowiss. Fak., Diss., 1976. (Nicht f. d. Austausch.).
Sliter, William V, Bé, Allan W. H, Berger, Wolfgang
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Zeitz, Christina, Kloeckener-Gruissem, Barbara, Forster, Ursula, Kohl, Susanne, Magyar, István, Wissinger, Bernd, ...
Mutations in genes encoding either components of the phototransduction cascade or proteins presumably involved in signaling from photoreceptors to adjacent second-order neurons have been shown to...
Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy
Wycisk, Katharina Agnes, Zeitz, Christina, Feil, Silke, Wittmer, Mariana, Forster, Ursula, Neidhardt, John, ...
Retinal signal transmission depends on the activity of high voltage–gated l-type calcium channels in photoreceptor ribbon synapses. We recently identified a truncating frameshift mutation in the...
Senn, Oliver, Russi, Erich W, Schindler, Christian, Imboden, Medea, Von Eckardstein, Arnold, Brändli, Otto, ...
Probst-Hensch, Nicole M., Imboden, Medea, Dietrich, Denise Felber, Barthélemy, Jean-Claude, Ackermann-Liebrich, Ursula, Berger, Wolfgang, ...
Kloeckener-Gruissem, Barbara, Vandekerckhove, Kristof, Nürnberg, Gudrun, Neidhardt, John, Zeitz, Christina, Nürnberg, Peter, ...
Unobstructed vision requires a particular refractive index of the lens, a measure based on the organization of the structural proteins within the differentiated lens cells. To ensure an intact lens...