24 results for author:"Stucka R." in Literature citations
Results Customize
› Repeat search in UniProtKB (483)
| Clinical and neuropathological findings in patients with TACO1 mutations. Seeger J., Schrank B., Pyle A., Stucka R., Lorcher U., Muller-Ziermann S., Abicht A., Czermin B., Holinski-Feder E., Lochmuller H. et al. Neuromuscul. Disord. 20:720-724(2010) · Mapped (2) |
| Intragenic deletion of TRIM32 in compound heterozygotes with sarcotubular myopathy/LGMD2H. Borg K., Stucka R., Locke M., Melin E., Ahlberg G., Klutzny U., Hagen M., Huebner A., Lochmuller H., Wrogemann K. et al. Hum. Mutat. 30:E831-44(2009) · Mapped (1) |
| An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndrome. Muller J.S., Stucka R., Neudecker S., Zierz S., Schmidt C., Huebner A., Lochmuller H., Abicht A. Neurology 65:463-465(2005) · Mapped (2) |
| A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndrome. Muller J.S., Abicht A., Christen H.J., Stucka R., Schara U., Mortier W., Huebner A., Lochmuller H. Neuromuscul. Disord. 14:744-749(2004) · Mapped (1) |
| Expression of dystrophin driven by the 1.35-kb MCK promoter ameliorates muscular dystrophy in fast, but not in slow muscles of transgenic mdx mice. Dunant P., Larochelle N., Thirion C., Stucka R., Ursu D., Petrof B.J., Wolf E., Lochmuller H. Mol. Ther. 8:80-89(2003) · Mapped (8) |
| Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patients. Mueller J.S., Mildner G., Mueller-Felber W., Schara U., Krampfl K., Petersen B., Petrova S., Stucka R., Mortier W., Bufler J. et al. Neurology 60:1805-1810(2003) · UniProtKB (1) |
| Congenital myasthenic syndrome due to a novel missense mutation in the gene encoding choline acetyltransferase. Schmidt C., Abicht A., Krampfl K., Voss W., Stucka R., Mildner G., Petrova S., Schara U., Mortier W., Bufler J. et al. Neuromuscul. Disord. 13:245-251(2003) · Mapped (8) |
| Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts. Jaksch M., Paret C., Stucka R., Horn N., Muller-Hocker J., Horvath R., Trepesch N., Stecker G., Freisinger P., Thirion C. et al. Hum. Mol. Genet. 10:3025-3035(2001) · Mapped (1) |
| Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscle. Thirion C., Stucka R., Mendel B., Gruhler A., Jaksch M., Nowak K.J., Binz N., Laing N.G., Lochmuller H. Eur. J. Biochem. 268:3473-3482(2001) · UniProtKB (1) |
| Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency. Horvath R., Lochmuller H., Stucka R., Yao J., Shoubridge E.A., Kim S.-H., Gerbitz K.-D., Jaksch M. Biochem. Biophys. Res. Commun. 276:530-533(2000) · UniProtKB (1) |
| The fdp1 and cif1 mutations are caused by different single nucleotide changes in the yeast CIF1 gene. Stucka R., Blazquez M.A. FEMS Microbiol. Lett. 107:251-253(1993) · Mapped (1) |
| Trehalose-6-P synthase is dispensable for growth on glucose but not for spore germination in Schizosaccharomyces pombe. Blazquez M.A., Stucka R., Feldmann H., Gancedo C. J. Bacteriol. 176:3895-3902(1994) · UniProtKB (1) · Mapped (1) |
| Analysis of a 70 kb region on the right arm of yeast chromosome II. Mannhaupt G., Stucka R., Ehnle S., Vetter I., Feldmann H. |
| Complete DNA sequence of yeast chromosome II. Feldmann H., Aigle M., Aljinovic G., Andre B., Baclet M.C., Barthe C., Baur A., Becam A.-M., Biteau N., Boles E. et al. |
| Identification of a set of yeast genes coding for a novel family of putative ATPases with high similarity to constituents of the 26S protease complex. Schnall R., Mannhaupt G., Stucka R., Tauer R., Ehnle S., Schwarzlose C., Vetter I., Feldmann H. Yeast 10:1141-1155(1994) · UniProtKB (14) |
| Nucleotide sequence of the phosphoenolpyruvate carboxykinase gene from Saccharomyces cerevisiae. Stucka R., Veldes-Hevia K.D., Gancedo C., Feldmann H. Nucleic Acids Res. 16:10926-10926(1988) · UniProtKB (1) |
| Characterization of the prephenate dehydrogenase-encoding gene, TYR1, from Saccharomyces cerevisiae. Mannhaupt G., Stucka R., Pilz U., Schwarzlose C., Feldmann H. Gene 85:303-311(1989) · UniProtKB (1) |
| Sequence of a cDNA clone encompassing the complete mature human prostate specific antigen (PSA) and an unspliced leader sequence. Schulz P., Stucka R., Feldmann H., Combriato G., Klobeck H.-G., Fittler F. Nucleic Acids Res. 16:6226-6226(1988) · UniProtKB (1) |
| An element of symmetry in yeast TATA-box binding protein transcription factor IID. Consequence of an ancestral duplication? Stucka R., Feldmann H. FEBS Lett. 261:223-225(1990) · Mapped (1) |
| DNA sequences in chromosomes II and VII code for pyruvate carboxylase isoenzymes in Saccharomyces cerevisiae: analysis of pyruvate carboxylase-deficient strains. Stucka R., Dequin S., Salmon J.-M., Gancedo C. Mol. Gen. Genet. 229:307-315(1991) · UniProtKB (1) · Mapped (1) |
| Molecular analysis of yeast chromosome II between CMD1 and LYS2: the excision repair gene RAD16 located in this region belongs to a novel group of double-finger proteins. Mannhaupt G., Stucka R., Ehnle S., Vetter I., Feldmann H. |
| Molecular analysis of the yeast Ty4 element: homology with Ty1, copia, and plant retrotransposons. Stucka R., Schwarzlose C., Lochmuller H., Hacker U., Feldmann H. Gene 122:119-128(1992) · Mapped (2) |
| Molecular cloning of CIF1, a yeast gene necessary for growth on glucose. Gonzales M.I., Stucka R., Blazquez M.A., Feldmann H., Gancedo C. |
| DIT101 (CSD2, CAL1), a cell cycle-regulated yeast gene required for synthesis of chitin in cell walls and chitosan in spore walls. Pammer M., Briza P., Ellinger A., Schuster T., Stucka R., Feldmann H., Breitenbach M. Yeast 8:1089-1099(1992) · Mapped (2) |