Abnormal calcium homeostasis in fibroblasts from patients with Leigh disease

Biochemical and Biophysical Research Communications

Volumn 283, Issue 3, 2001, Pages 687-693

  Wasniewska, Magdalena ^a   Karczmarewicz, Elzbieta ^a,b   Pronicki, Maciej ^b   Piekutowska Abramczuk, Dorota ^b   Zablocki, Krzysztof ^a   Popowska, Ewa ^b   Pronicka, Ewa ^b   Duszyński, Jerzy ^a  

^a NENCKI INSTITUTE OF EXPERIMENTAL BIOLOGY   (Poland)

^b CHILDREN'S MEMORIAL HEALTH INSTITUTE   (Poland)

Author keywords

Calcium homeostasis; Leigh syndrome; Mitochondrial diseases; SOCs; SURF 1

Indexed keywords

CALCIUM CHANNEL; CALCIUM ION; CYTOCHROME C OXIDASE; GENE PRODUCT; PROTEIN SURF1; THAPSIGARGIN; UNCLASSIFIED DRUG;

ARTICLE; CALCIUM HOMEOSTASIS; CALCIUM METABOLISM; CALCIUM TRANSPORT; CHILD; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; FEMALE; FIBROBLAST; GENE ISOLATION; GENE MUTATION; HISTOPATHOLOGY; HUMAN; HUMAN CELL; LEIGH DISEASE; MALE; MITOCHONDRIAL MEMBRANE; PRIORITY JOURNAL; SURF1 GENE;

EID: 0034811893     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.2001.4834     Document Type: Article

References (31)

1. Structural and functional aspects of calcium homeostasis in eucariotic cells
2. Store depletion and calcium influx
3. A model for receptor-regulated calcium entry
4. 2+ signaling requirements
5. Thapsigargin, a novel molecular probe for studying intracellular calcium release and storage
6. The role of mitochondria in the regulation of calcium influx into Jurkat cells
7. The role of mitochondrial dysfunction in regulation of store-operated calcium channels in glioma C6 and human fibroblast cells
8. 2+ to mitochondria
9. Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiency
10. Surf-1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome
11. Genetic heterogeneity in Leigh syndrome
12. Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent diaminobenzidine (DAB)
13. Analytical reliability of spectrophotometric analysis of the activity of mitochondrial respiratory chain complexes in muscle homogenates
14. Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency
15. 2+ indicators with greatly improved fluorescence properties
16. 2+ influx dependent on store depletion by intracellular adenine-guanine nucleotide levels
17. 3 and dissociation from calcium release
18. The calcium entry pas de deux
19. Inositol 1,3,4,5-tetrakisphosphate activates an endothelial calcium-permeable channel
20. 2+ entry by two different pathways in hepatocytes
21. + current by means of small diffusible messenger
22. 2+ influx
23. G-protein regulation of capacitative calcium entry may be mediated by protein kinases A and C in Xenopus oocytes
24. 2+ permeability according to the filling state of the intracellular calcium stores
25. Capacitative calcium entry is inhibited in vascular endothelial cells by disruption of cytoskeletal microfilaments
26. Role of the cytoskeleton in calcium signaling in NIH 3T3 cells
27. 2+ entry by tyrosine kinase inhibitors
28. 2+ inflow in Xenopus laevis oocytes: Inhibition by primaquine and evaluation of the role of membrane fusion
29. Mitochondrial regulation of store-operated calcium signaling in T lymphocytes
30. Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutations for myoclonus epilepsy with ragged red fibers ("MERRF") at position 8344 nt
31. Subacute necrotizing encephalomyelopathy in an infant