Robinson BH - Search Results

1

Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: a comparison of subunit proteins in normal fibroblasts treated with ethidium bromide and fibroblasts from a patient with mtDNA depletion syndrome.

Marusich MF, Robinson BH, Taanman JW, Kim SJ, Schillace R, Smith JL, Capaldi RA. Marusich MF, et al. Among authors: robinson bh. Biochim Biophys Acta. 1997 Dec 31;1362(2-3):145-59. doi: 10.1016/s0925-4439(97)00061-6. Biochim Biophys Acta. 1997. PMID: 9540845 Free article.

2

Structure, functioning, and assembly of the ATP synthase in cells from patients with the T8993G mitochondrial DNA mutation. Comparison with the enzyme in Rho(0) cells completely lacking mtdna.

García JJ, Ogilvie I, Robinson BH, Capaldi RA. García JJ, et al. Among authors: robinson bh. J Biol Chem. 2000 Apr 14;275(15):11075-81. doi: 10.1074/jbc.275.15.11075. J Biol Chem. 2000. PMID: 10753912 Free article.

3

Cytochrome c oxidase-deficient patients have distinct subunit assembly profiles.

Hanson BJ, Carrozzo R, Piemonte F, Tessa A, Robinson BH, Capaldi RA. Hanson BJ, et al. Among authors: robinson bh. J Biol Chem. 2001 May 11;276(19):16296-301. doi: 10.1074/jbc.M011162200. Epub 2001 Feb 7. J Biol Chem. 2001. PMID: 11278850 Free article.

4

Characterization of cytochrome-c oxidase mutants in human fibroblasts.

Glerum DM, Yanamura W, Capaldi RA, Robinson BH. Glerum DM, et al. Among authors: robinson bh. FEBS Lett. 1988 Aug 15;236(1):100-4. doi: 10.1016/0014-5793(88)80293-x. FEBS Lett. 1988. PMID: 2841159 Free article.

5

The use of skin fibroblast cultures in the detection of respiratory chain defects in patients with lacticacidemia.

Robinson BH, Glerum DM, Chow W, Petrova-Benedict R, Lightowlers R, Capaldi R. Robinson BH, et al. Pediatr Res. 1990 Nov;28(5):549-55. doi: 10.1203/00006450-199011000-00027. Pediatr Res. 1990. PMID: 2175027

6

Saguenay Lac Saint Jean cytochrome oxidase deficiency: sequence analysis of nuclear encoded COX subunits, chromosomal localization and a sequence anomaly in subunit VIc.

Lee N, Morin C, Mitchell G, Robinson BH. Lee N, et al. Among authors: robinson bh. Biochim Biophys Acta. 1998 Feb 27;1406(1):1-4. doi: 10.1016/s0925-4439(98)00003-9. Biochim Biophys Acta. 1998. PMID: 9545512 Free article.

7

Lacticacidemia.

Robinson BH. Robinson BH. Biochim Biophys Acta. 1993 Oct 20;1182(3):231-44. doi: 10.1016/0925-4439(93)90064-8. Biochim Biophys Acta. 1993. PMID: 8399357 Review. No abstract available.

8

Automated spectrophotometric analysis of mitochondrial respiratory chain complex enzyme activities in cultured skin fibroblasts.

Kramer KA, Oglesbee D, Hartman SJ, Huey J, Anderson B, Magera MJ, Matern D, Rinaldo P, Robinson BH, Cameron JM, Hahn SH. Kramer KA, et al. Among authors: robinson bh. Clin Chem. 2005 Nov;51(11):2110-6. doi: 10.1373/clinchem.2005.050146. Epub 2005 Sep 1. Clin Chem. 2005. PMID: 16141288

9

Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunction.

Raha S, Merante F, Shoubridge E, Myint AT, Tein I, Benson L, Johns T, Robinson BH. Raha S, et al. Among authors: robinson bh. Hum Mutat. 1999;13(3):245-54. doi: 10.1002/(SICI)1098-1004(1999)13:3<245::AID-HUMU9>3.0.CO;2-B. Hum Mutat. 1999. PMID: 10090480

10

Human complex I deficiency: clinical spectrum and involvement of oxygen free radicals in the pathogenicity of the defect.

Robinson BH. Robinson BH. Biochim Biophys Acta. 1998 May 6;1364(2):271-86. doi: 10.1016/s0005-2728(98)00033-4. Biochim Biophys Acta. 1998. PMID: 9593934 Free article. Review. No abstract available.

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