Wolfgang Berger

Circulating alpha1-antitrypsin in the general population: Determinants and association with lung function (2008)

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...

Glutathione S-transferase genotypes modify lung function decline in the general population: SAPALDIA cohort study (2007)

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...

Mice Null for Frizzled4 (Fzd4−/−) Are Infertile and Exhibit Impaired Corpora Lutea Formation and Function1 (2005)

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...

Einfluss eines Benzodiazepines sowie eines Phytopharmakons auf emotionale Befindlichkeit und kognitive Leistungsfähigkeit (2005)

Berger, Wolfgang

Die vorliegende pharmakopsychologische Studie wurde als explorative Kontrolluntersuchung zur Studie „Influence of Valerian Treatment on Reaction Time, Alertness and Concentration in Volunteers“...

NYX (Nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein (2003)

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...

NYX (Nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein (2003)

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...

Global Gene Expression Analysis in a Mouse Model for Norrie Disease: Late Involvement of Photoreceptor Cells (2002)

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,...

Global Gene Expression Analysis in a Mouse Model for Norrie Disease: Late Involvement of Photoreceptor Cells (2002)

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,...

X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications (2001)

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...

The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors (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...

Lebensdauervorhersage fur partikelverstaerkte Aluminiumlegierungen unter Beruecksichtigung der mikrostrukturellen Aspekte der Schaedigung (Working Life Predictions for Particle-Strengthened Aluminum Alloy with Regard to Microstructural Aspects of Deterioration) (1998)

Berger, Wolfgang

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)

Berger, Wolfgang.

Beitr. teilw. dt., teilw. engl. - Enth. 16 Sonderabdr. aus verschiedenen Zeitschr.

Die manuelle Aknetherapie / (1995)

Berger, Wolfgang.

München, Techn. Univ., Diss., 1995.

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...

Der Akute rechte Unterbauch differentialdiagnostische Schwierigkeiten / (1987)

Berger, Wolfgang.

Thesis (doctoral)--Rheinische Friedrich-Wilhelms-Universität zu Bonn, 1987.

Grundlagen der Arbeitsweise schwingender Aufbereitungsherde / (1960)

Berger, Wolfgang.

Erschien vollständ. als Diss., Bergakademie Freiberg.

Grundlagen der Arbeitsweise schwingender Aufbereitungsherde. (1959)

Berger, Wolfgang.

Dass. Autorreferat. 1 Bl. 4 - Aus: Bergakademie. 1959, H. 11, S. 674-675

Die betriebswirtschaftliche Kostentheorie und ihre Bedeutung für die Planwirtschaft. (1949)

Berger, Wolfgang.

Leipzig, Gesellschaftswiss. F., Diss. v. 13. Sept. 1949 (Nicht f. d. Austausch).

Über Geschosswanderung im Kreislaufsystem. (1943)

Berger, Wolfgang.

Tübingen, Med. F., Diss., 1943 (Nicht f. d. Austausch).

Mutations in CABP4, the Gene Encoding the Ca2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness

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...

Mutation of Solute Carrier SLC16A12 Associates with a Syndrome Combining Juvenile Cataract with Microcornea and Renal Glucosuria

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...