» Articles » PMID: 1293397

Selective Killing of Cells with Oxidative Defects in Galactose Medium: a Screening Test for Affected Patient Fibroblasts

Overview
Publisher Wiley
Date 1992 Jan 1
PMID 1293397
Citations 6
Authors
Affiliations
Soon will be listed here.
Citing Articles

A Novel Family of Lysosomotropic Tetracyclic Compounds for Treating Leukemia.

Carbo J, Cornet-Masana J, Cuesta-Casanovas L, Delgado-Martinez J, Banus-Mulet A, Clement-Demange L Cancers (Basel). 2023; 15(6).

PMID: 36980800 PMC: 10047683. DOI: 10.3390/cancers15061912.


Relevance of the TRIAP1/p53 axis in colon cancer cell proliferation and adaptation to glutamine deprivation.

Nedara K, Reinhardt C, Lebraud E, Arena G, Gracia C, Buard V Front Oncol. 2022; 12:958155.

PMID: 36387192 PMC: 9661196. DOI: 10.3389/fonc.2022.958155.


Nutritional Interventions for Mitochondrial OXPHOS Deficiencies: Mechanisms and Model Systems.

Kuszak A, Espey M, Falk M, Holmbeck M, Manfredi G, Shadel G Annu Rev Pathol. 2017; 13:163-191.

PMID: 29099651 PMC: 5911915. DOI: 10.1146/annurev-pathol-020117-043644.


Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy.

Kopajtich R, Nicholls T, Rorbach J, Metodiev M, Freisinger P, Mandel H Am J Hum Genet. 2014; 95(6):708-20.

PMID: 25434004 PMC: 4259976. DOI: 10.1016/j.ajhg.2014.10.017.


NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological disease.

Pitceathly R, Rahman S, Wedatilake Y, Polke J, Cirak S, Foley A Cell Rep. 2013; 3(6):1795-805.

PMID: 23746447 PMC: 3701321. DOI: 10.1016/j.celrep.2013.05.005.


References
1.
Day C, Scheffler I . Mapping of the genes of some components of the electron transport chain (complex I) on the X chromosome of mammals. Somatic Cell Genet. 1982; 8(6):691-707. DOI: 10.1007/BF01543012. View

2.
Soderberg K, Nissinen E, BAKAY B, Scheffler I . The energy charge in wild-type and respiration-deficient Chinese hamster cell mutants. J Cell Physiol. 1980; 103(1):169-72. DOI: 10.1002/jcp.1041030121. View

3.
Robinson B, Macmillan H, Sherwood W . Variable clinical presentation in patients with defective E1 component of pyruvate dehydrogenase complex. J Pediatr. 1987; 111(4):525-33. DOI: 10.1016/s0022-3476(87)80112-9. View

4.
JOHNS D, Berman J . Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy. Biochem Biophys Res Commun. 1991; 174(3):1324-30. DOI: 10.1016/0006-291x(91)91567-v. View

5.
Robinson B, Glerum D, Chow W, Lightowlers R, Capaldi R . The use of skin fibroblast cultures in the detection of respiratory chain defects in patients with lacticacidemia. Pediatr Res. 1990; 28(5):549-55. DOI: 10.1203/00006450-199011000-00027. View