Rustin P - Search Results

1

Mitochondrial respiratory chain dysfunction caused by coenzyme Q deficiency.

Rustin P, Munnich A, Rötig A. Rustin P, et al. Methods Enzymol. 2004;382:81-8. doi: 10.1016/S0076-6879(04)82005-6. Methods Enzymol. 2004. PMID: 15047097 Review. No abstract available.

2

Coenzyme Q10 depletion is comparatively less detrimental to human cultured skin fibroblasts than respiratory chain complex deficiencies.

Geromel V, Rötig A, Munnich A, Rustin P. Geromel V, et al. Among authors: rustin p. Free Radic Res. 2002 Apr;36(4):375-9. doi: 10.1080/10715760290021216. Free Radic Res. 2002. PMID: 12069100

3

Expressed sequence tag database screening for identification of human genes.

Rötig A, Munnich A, Rustin P. Rötig A, et al. Among authors: rustin p. Methods Enzymol. 2002;353:566-74. doi: 10.1016/s0076-6879(02)53077-9. Methods Enzymol. 2002. PMID: 12078528 No abstract available.

4

Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits.

Geromel V, Darin N, Chrétien D, Bénit P, DeLonlay P, Rötig A, Munnich A, Rustin P. Geromel V, et al. Among authors: rustin p. Mol Genet Metab. 2002 Sep-Oct;77(1-2):21-30. doi: 10.1016/s1096-7192(02)00145-2. Mol Genet Metab. 2002. PMID: 12359126 Review.

5

Cell complementation using Genebridge 4 human:rodent hybrids for physical mapping of novel mitochondrial respiratory chain deficiency genes.

De Lonlay P, Mugnier C, Sanlaville D, Chantrel-Groussard K, Bénit P, Lebon S, Chrétien D, Kadhom N, Saker S, Gyapay G, Romana S, Weissenbach J, Munnich A, Rustin P, Rötig A. De Lonlay P, et al. Among authors: rustin p. Hum Mol Genet. 2002 Dec 15;11(26):3273-81. doi: 10.1093/hmg/11.26.3273. Hum Mol Genet. 2002. PMID: 12471054

6

Assay of mitochondrial respiratory chain complex I in human lymphocytes and cultured skin fibroblasts.

Chretien D, Bénit P, Chol M, Lebon S, Rötig A, Munnich A, Rustin P. Chretien D, et al. Among authors: rustin p. Biochem Biophys Res Commun. 2003 Jan 31;301(1):222-4. doi: 10.1016/s0006-291x(02)03016-4. Biochem Biophys Res Commun. 2003. PMID: 12535666

7

Antenatal manifestations of mitochondrial respiratory chain deficiency.

von Kleist-Retzow JC, Cormier-Daire V, Viot G, Goldenberg A, Mardach B, Amiel J, Saada P, Dumez Y, Brunelle F, Saudubray JM, Chrétien D, Rötig A, Rustin P, Munnich A, De Lonlay P. von Kleist-Retzow JC, et al. Among authors: rustin p. J Pediatr. 2003 Aug;143(2):208-12. doi: 10.1067/S0022-3476(03)00130-6. J Pediatr. 2003. PMID: 12970634

8

Revisiting pitfalls, problems and tentative solutions for assaying mitochondrial respiratory chain complex III in human samples.

Chretien D, Slama A, Brière JJ, Munnich A, Rötig A, Rustin P. Chretien D, et al. Among authors: rustin p. Curr Med Chem. 2004 Jan;11(2):233-9. doi: 10.2174/0929867043456151. Curr Med Chem. 2004. PMID: 14754419 Review.

9

Respiratory chain deficiency presenting as congenital nephrotic syndrome.

Goldenberg A, Ngoc LH, Thouret MC, Cormier-Daire V, Gagnadoux MF, Chrétien D, Lefrançois C, Geromel V, Rötig A, Rustin P, Munnich A, Paquis V, Antignac C, Gubler MC, Niaudet P, de Lonlay P, Bérard E. Goldenberg A, et al. Among authors: rustin p. Pediatr Nephrol. 2005 Apr;20(4):465-9. doi: 10.1007/s00467-004-1725-4. Epub 2005 Jan 29. Pediatr Nephrol. 2005. PMID: 15682315

10

Another observation with VATER association and a complex IV respiratory chain deficiency.

Thauvin-Robinet C, Faivre L, Huet F, Journeau P, Glorion C, Rustin P, Rötig A, Munnich A, Cormier-Daire V. Thauvin-Robinet C, et al. Among authors: rustin p. Eur J Med Genet. 2006 Jan-Feb;49(1):71-7. doi: 10.1016/j.ejmg.2005.04.001. Eur J Med Genet. 2006. PMID: 16473312

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