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Results: 1-10 |
Results: 10
A novel mutation in SURF1 causes skipping of exon 8 in a patient with cytochrome c oxidase-deficient Leigh syndrome and hypertrichosis
Authors: Williams, SL Taanman, JW Hansikova, H Houst'kova, H Chowdhury, S Zeman, J Houstek, J
Citation: Sl. Williams et al., A novel mutation in SURF1 causes skipping of exon 8 in a patient with cytochrome c oxidase-deficient Leigh syndrome and hypertrichosis, MOL GEN MET, 73(4), 2001, pp. 340-343
Optimal conditions for determination of cytochrome c oxidase activity in the rat heart
Authors: Stieglerova, A Drahota, Z Ostadal, B Houstek, J
Citation: A. Stieglerova et al., Optimal conditions for determination of cytochrome c oxidase activity in the rat heart, PHYSL RES, 49(2), 2000, pp. 245-250
A novel principle for conferring selectivity to poly(A)-binding proteins: interdependence of two ATP synthase beta-subunit mRNA-binding proteins
Authors: Andersson, U Antonicka, H Houstek, J Cannon, B
Citation: U. Andersson et al., A novel principle for conferring selectivity to poly(A)-binding proteins: interdependence of two ATP synthase beta-subunit mRNA-binding proteins, BIOCHEM J, 346, 2000, pp. 33-39
Abnormalities in succinylpurines in fumarase deficiency: Possible role in pathogenesis of CNS impairment
Authors: Zeman, J Krijt, J Stratilova, L Hansikova, H Wenchich, L Kmoch, S Chrastina, P Houstek, J
Citation: J. Zeman et al., Abnormalities in succinylpurines in fumarase deficiency: Possible role in pathogenesis of CNS impairment, J INH MET D, 23(4), 2000, pp. 371-374
Activities of mitochondrial oxidative phosphorylation enzymes in cultured amniocytes
Authors: Chowdhury, SKR Drahota, Z Floryk, D Calda, P Houstek, J
Citation: Skr. Chowdhury et al., Activities of mitochondrial oxidative phosphorylation enzymes in cultured amniocytes, CLIN CHIM A, 298(1-2), 2000, pp. 157-173
Genetic aspects of mitochondrial encephalomyoptahies
Authors: Houstek, J
Citation: J. Houstek, Genetic aspects of mitochondrial encephalomyoptahies, BIOLOGIA, 55(3), 2000, pp. 209-221
A novel deficiency of mitochondrial ATPase of nuclear origin
Authors: Houstek, J Klement, P Floryk, D Antonicka, H Hermanska, J Kalous, M Hansikova, H Houst'kova, H Chowdhury, SKR Rosipal, S Kmoch, S Stratilova, L Zeman, J
Citation: J. Houstek et al., A novel deficiency of mitochondrial ATPase of nuclear origin, HUM MOL GEN, 8(11), 1999, pp. 1967-1974
Defective kinetics of cytochrome c oxidase sold alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres ('MERRF') at position8344 nt
Authors: Antonicka, H Floryk, D Klement, P Stratilova, L Hermanska, J Houstkova, H Kalous, M Drahota, Z Zeman, J Houstek, J
Citation: H. Antonicka et al., Defective kinetics of cytochrome c oxidase sold alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres ('MERRF') at position8344 nt, BIOCHEM J, 342, 1999, pp. 537-544
Complex approach to prenatal diagnosis of cytochrome c oxidase deficiencies
Authors: Houstek, J Klement, P Hermanska, J Antonicka, H Houstkova, H Stratilova, L Wanders, RJA Zeman, J
Citation: J. Houstek et al., Complex approach to prenatal diagnosis of cytochrome c oxidase deficiencies, PRENAT DIAG, 19(6), 1999, pp. 552-558
Tetramethyl rhodamine methyl ester (TMRM) is suitable for cytofluorometricmeasurements of mitochondrial membrane potential in cells treated with digitonin
Authors: Floryk, D Houstek, J
Citation: D. Floryk et J. Houstek, Tetramethyl rhodamine methyl ester (TMRM) is suitable for cytofluorometricmeasurements of mitochondrial membrane potential in cells treated with digitonin, BIOSCI REP, 19(1), 1999, pp. 27-34
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