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	1.	Activation of cryptic splice sites is a frequent splicing defect mechanism caused by mutations in exon and intron sequences of the OPA1 gene. [electronic resource] by Schimpf, Simone Schaich, Simone Wissinger, Bernd Producer: 20070309 In: Human genetics vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Comprehensive cDNA study and quantitative transcript analysis of mutant OPA1 transcripts containing premature termination codons. [electronic resource] by Schimpf, Simone Fuhrmann, Nico Schaich, Simone Wissinger, Bernd Producer: 20080206 In: Human mutation vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy. [electronic resource] by Dadgar, Sharareh Hagens, Olivier Dadgar, Seyed Razi Haghighi, Ehsan Nobakht Schimpf, Simone Wissinger, Bernd Garshasbi, Masoud Producer: 20061106 In: Experimental eye research vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy. [electronic resource] by Fuhrmann, Nico Schimpf, Simone Kamenisch, York Leo-Kottler, Beate Alexander, Christiane Auburger, Georg Zrenner, Eberhart Wissinger, Bernd Alavi, Marcel V Producer: 20110714 In: Molecular neurodegeneration vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy. [electronic resource] by Lodi, Raffaele Tonon, Caterina Valentino, Maria Lucia Iotti, Stefano Clementi, Valeria Malucelli, Emil Barboni, Piero Longanesi, Lora Schimpf, Simone Wissinger, Bernd Baruzzi, Agostino Barbiroli, Bruno Carelli, Valerio Producer: 20050110 In: Annals of neurology vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. [electronic resource] by Zanna, Claudia Ghelli, Anna Porcelli, Anna Maria Karbowski, Mariusz Youle, Richard J Schimpf, Simone Wissinger, Bernd Pinti, Marcello Cossarizza, Andrea Vidoni, Sara Valentino, Maria Lucia Rugolo, Michela Carelli, Valerio Producer: 20080423 In: Brain : a journal of neurology vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	'Behr syndrome' with OPA1 compound heterozygote mutations. [electronic resource] by Carelli, Valerio Sabatelli, Mario Carrozzo, Rosalba Rizza, Teresa Schimpf, Simone Wissinger, Bernd Zanna, Claudia Rugolo, Michela La Morgia, Chiara Caporali, Leonardo Carbonelli, Michele Barboni, Piero Tonon, Caterina Lodi, Raffaele Bertini, Enrico Producer: 20150302 In: Brain : a journal of neurology vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	OPA1 mutations associated with dominant optic atrophy influence optic nerve head size. [electronic resource] by Barboni, Piero Carbonelli, Michele Savini, Giacomo Foscarini, Beatrice Parisi, Vincenzo Valentino, Maria L Carta, Arturo De Negri, Annamaria Sadun, Federico Zeviani, Massimo Sadun, Alfredo A Schimpf, Simone Wissinger, Bernd Carelli, Valerio Producer: 20100826 In: Ophthalmology vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy. [electronic resource] by Alavi, Marcel V Bette, Stefanie Schimpf, Simone Schuettauf, Frank Schraermeyer, Ulrich Wehrl, Hans F Ruttiger, Lukas Beck, Susanne C Tonagel, Felix Pichler, Bernd J Knipper, Marlies Peters, Thomas Laufs, Juergen Wissinger, Bernd Producer: 20070530 In: Brain : a journal of neurology vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutations. [electronic resource] by Lodi, Raffaele Tonon, Caterina Valentino, Maria Lucia Manners, David Testa, Claudia Malucelli, Emil La Morgia, Chiara Barboni, Piero Carbonelli, Michele Schimpf, Simone Wissinger, Bernd Zeviani, Massimo Baruzzi, Agostino Liguori, Rocco Barbiroli, Bruno Carelli, Valerio Producer: 20110214 In: Archives of neurology vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. [electronic resource] by Carelli, Valerio Schimpf, Simone Fuhrmann, Nico Valentino, Maria Lucia Zanna, Claudia Iommarini, Luisa Papke, Monika Schaich, Simone Tippmann, Sabine Baumann, Britta Barboni, Piero Longanesi, Lora Rugolo, Michela Ghelli, Anna Alavi, Marcel V Youle, Richard J Bucchi, Laura Carroccia, Rosanna Giannoccaro, Maria Pia Tonon, Caterina Lodi, Raffaele Cenacchi, Giovanna Montagna, Pasquale Liguori, Rocco Wissinger, Bernd Producer: 20110809 In: Human molecular genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)