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Results: 1-8 |
Results: 8

Authors: ELMEZIANE A LEHTINEN SK HANCE N NIJTMANS LGJ DUNBAR D HOLT IJ JACOBS HT
Citation: A. Elmeziane et al., A TRANSFER-RNA SUPPRESSOR MUTATION IN HUMAN MITOCHONDRIA, Nature genetics, 18(4), 1998, pp. 350-353

Authors: NIJTMANS LGJ TAANMAN JW MUIJSERS AO SPEIJER D VANDENBOGERT C
Citation: Lgj. Nijtmans et al., ASSEMBLY OF CYTOCHROME-C-OXIDASE IN CULTURED HUMAN-CELLS, European journal of biochemistry, 254(2), 1998, pp. 389-394

Authors: LINCKE CR VANDENBOGERT C NIJTMANS LGJ WANDERS RJA TAMMINGA P BARTH PG
Citation: Cr. Lincke et al., CEREBELLAR HYPOPLASIA IN RESPIRATORY-CHAIN DYSFUNCTION, Neuropediatrics, 27(4), 1996, pp. 216-218

Authors: NIJTMANS LGJ KLEMENT P HOUSTEK J VANDENBOGERT C
Citation: Lgj. Nijtmans et al., ASSEMBLY OF MITOCHONDRIAL ATP SYNTHASE IN CULTURED HUMAN-CELLS - IMPLICATIONS FOR MITOCHONDRIAL DISEASES, Biochimica et biophysica acta. Molecular basis of disease, 1272(3), 1995, pp. 190-198

Authors: NIJTMANS LGJ BARTH PG LINCKE CR VANGALEN MJM ZWART R KLEMENT P BOLHUIS PA RUITENBEEK W WANDERS RJA VANDENBOGERT C
Citation: Lgj. Nijtmans et al., ALTERED KINETICS OF CYTOCHROME-C-OXIDASE IN A PATIENT WITH SEVERE MITOCHONDRIAL ENCEPHALOMYOPATHY, Biochimica et biophysica acta. Molecular basis of disease, 1270(2-3), 1995, pp. 193-201

Authors: NIJTMANS LGJ SPELBRINK JN VANGALEN MJM ZWAAN M KLEMENT P VANDENBOGERT C
Citation: Lgj. Nijtmans et al., EXPRESSION AND FATE OF THE NUCLEARLY ENCODED SUBUNITS OF CYTOCHROME-C-OXIDASE IN CULTURED HUMAN-CELLS DEPLETED OF MITOCHONDRIAL GENE-PRODUCTS, Biochimica et biophysica acta. Molecular cell research, 1265(2-3), 1995, pp. 117-126

Authors: KLEMENT P NIJTMANS LGJ VANDENBOGERT C HOUSTEK J
Citation: P. Klement et al., ANALYSIS OF OXIDATIVE-PHOSPHORYLATION COMPLEXES IN CULTURED HUMAN FIBROBLASTS AND AMNIOCYTES BY BLUE-NATIVE-ELECTROPHORESIS USING MITOPLASTS ISOLATED WITH THE HELP OF DIGITONIN, Analytical biochemistry, 231(1), 1995, pp. 218-224

Authors: OOSTRA RJ VANDENBOGERT C NIJTMANS LGJ VANGALEN MJM ZWART R BOLHUIS PA BLEEKERWAGEMAKERS EM
Citation: Rj. Oostra et al., SIMULTANEOUS OCCURRENCE OF THE 11778 (ND4) AND THE 9438 (COX-111) MTDNA MUTATIONS IN LEBER HEREDITARY OPTIC NEUROPATHY - MOLECULAR, BIOCHEMICAL, AND CLINICAL FINDINGS, American journal of human genetics, 57(4), 1995, pp. 954-957
Risultati: 1-8 |