OPA1 , encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
Wissinger, Bernd, Votruba, Marcela, Bhattacharya, Shomi S, Moore, Anthony, Leo-Kottler, Beate, Mayer, Simone, Pesch, Ulrike E.A, Alexander, Christiane, Thiselton, Dawn L, Kellner, Ulrich, Rodriguez, Miguel, Auburger, Georg
Published in Nature genetics (01.10.2000)
Published in Nature genetics (01.10.2000)
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Characterization of OPA1 isoforms isolated from mouse tissues
Akepati, Vasudheva Reddy, Müller, Eva-Christina, Otto, Albrecht, Strauss, Holger M, Portwich, Michael, Alexander, Christiane
Published in Journal of neurochemistry (01.07.2008)
Published in Journal of neurochemistry (01.07.2008)
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Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy
Fuhrmann, Nico, Schimpf, Simone, Kamenisch, York, Leo-Kottler, Beate, Alexander, Christiane, Auburger, Georg, Zrenner, Eberhart, Wissinger, Bernd, Alavi, Marcel V
Published in Molecular neurodegeneration (14.06.2010)
Published in Molecular neurodegeneration (14.06.2010)
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Lactobacillus paracasei DSMZ16671 Reduces Mutans Streptococci: A Short-Term Pilot Study
Holz, Caterina, Alexander, Christiane, Balcke, Christina, Moré, Margret, Auinger, Annegret, Bauer, Maren, Junker, Lauren, Grünwald, Jörg, Lang, Christine, Pompejus, Markus
Published in Probiotics and antimicrobial proteins (2013)
Published in Probiotics and antimicrobial proteins (2013)
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A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population : evidence for a founder effect
THISELTON, Dawn L, ALEXANDER, Christiane, MORRIS, Alex, BROOKS, Simon, ROSENBERG, Thomas, EIBERG, Hans, KJER, Birgit, KJER, Poul, BHATTACHARYA, Shomi S, VOTRUBA, Marcela
Published in Human genetics (01.11.2001)
Published in Human genetics (01.11.2001)
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SLP-2 is required for stress-induced mitochondrial hyperfusion
Tondera, Daniel, Grandemange, Stéphanie, Jourdain, Alexis, Karbowski, Mariusz, Mattenberger, Yves, Herzig, Sébastien, Da Cruz, Sandrine, Clerc, Pascaline, Raschke, Ines, Merkwirth, Carsten, Ehses, Sarah, Krause, Frank, Chan, David C, Alexander, Christiane, Bauer, Christoph, Youle, Richard, Langer, Thomas, Martinou, Jean-Claude
Published in The EMBO journal (03.06.2009)
Published in The EMBO journal (03.06.2009)
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Journal Article
OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance
PESCH, Ulrike E. A, LEO-KOTTLER, Beate, MAYER, Simone, JURKLIES, Bernhard, KELLNER, Ulrich, APFELSTEDT-SYLLA, Eckart, ZRENNER, Eberhart, ALEXANDER, Christiane, WISSINGER, Bernd
Published in Human molecular genetics (15.06.2001)
Published in Human molecular genetics (15.06.2001)
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A Comprehensive Survey of Mutations in the OPA1 Gene in Patients with Autosomal Dominant Optic Atrophy
Thiselton, Dawn L, Alexander, Christiane, Taanman, Jan-Willem, Brooks, Simon, Rosenberg, Thomas, Eiberg, Hans, Andreasson, Sten, Van Regemorter, Nicole, Munier, Francis L, Moore, Anthony T, Bhattacharya, Shomi S, Votruba, Marcela
Published in Investigative ophthalmology & visual science (01.06.2002)
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Published in Investigative ophthalmology & visual science (01.06.2002)
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OPA1, the Disease Gene for Autosomal Dominant Optic Atrophy, Is Specifically Expressed in Ganglion Cells and Intrinsic Neurons of the Retina
Pesch, Ulrike E. A, Fries, Julia E, Bette, Stefanie, Kalbacher, Hubert, Wissinger, Bernd, Alexander, Christiane, Kohler, Konrad
Published in Investigative ophthalmology & visual science (01.11.2004)
Published in Investigative ophthalmology & visual science (01.11.2004)
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A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene
AUNG, Tin, OCAKA, Louise, FRANCIS, Peter J, HITCHINGS, Roger A, LEHMANN, Ordan J, BHATTACHARYA, Shomi S, EBENEZER, Neil D, MORRIS, Alex G, KRAWCZAK, Michael, THISELTON, Dawn L, ALEXANDER, Christiane, VOTRUBA, Marcela, BRICE, Glen, CHILD, Anne H
Published in Human genetics (2002)
Published in Human genetics (2002)
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Identification of the Physiological Promoter for Spinocerebellar Ataxia 2 Gene Reveals a CpG Island for Promoter Activity Situated into the Exon 1 of This Gene and Provides Data about the Origin of the Nonmethylated State of These Types of Islands
Aguiar, Jorge, Santurlidis, Simon, Nowok, Joachim, Alexander, Christiane, Rudnicki, Doda, Gispert, Suzana, Schulz, Wolfgang, Auburger, Georg
Published in Biochemical and biophysical research communications (19.01.1999)
Published in Biochemical and biophysical research communications (19.01.1999)
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Fine scale mapping places DLG1, the gene encoding hDlg, telomeric to the OPA1 candidate region
Alexander, C, Stathakis, D G, Lin, L, Rahman, S, Bryant, P J, Auburger, G, Chishti, A H
Published in Mammalian genome (01.10.1997)
Published in Mammalian genome (01.10.1997)
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Year of Publication 30.01.2014
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Year of Publication 30.01.2014
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LITHOGRAPHIC DEVICE AND METHOD FOR MANUFACTURING DEVICE
JANSEN HANS, ALEKSEY YURIEVICH KOLENSNYCHENKO, HELMAR VAN SANTEN, FRANCISCUS JOHANNES HERMAN MARIA TEUNISSEN, CHRISTIANE ALEXANDER HOGENDAM, BOB STREEFKERK, JOHANNES JACOBS MATEUS BASELMANS, SECHELT NICHOLAS LAMBELDUS DONDERS, JEROEN JOHANNES SOPHIA MARIA MERTENS, JOHANNES CATHARINUS HUBERTUS MULKENS, FELIX GOTTFRIED PETER PETERS
Year of Publication 08.12.2011
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Year of Publication 08.12.2011
Patent