Ruiter JP - Search Results

1

Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder.

Chinopoulos C, Batzios S, van den Heuvel LP, Rodenburg R, Smeets R, Waterham HR, Turkenburg M, Ruiter JP, Wanders RJA, Doczi J, Horvath G, Dobolyi A, Vargiami E, Wevers RA, Zafeiriou D. Chinopoulos C, et al. Among authors: ruiter jp. Mol Genet Metab. 2019 Jan;126(1):43-52. doi: 10.1016/j.ymgme.2018.11.009. Epub 2018 Nov 16. Mol Genet Metab. 2019. PMID: 30470562

2

Prenatal diagnosis of systemic disorders of the respiratory chain in cultured amniocytes and chorionic villus fibroblasts by studying the formation of lactate and pyruvate from glucose.

Wanders RJ, Wijburg FA, Ruiter J, Trijbels JM, Ruitenbeek W, Sengers RC, Bakkeren JA, Feller N. Wanders RJ, et al. J Inherit Metab Dis. 1992;15(1):84-91. doi: 10.1007/BF01800349. J Inherit Metab Dis. 1992. PMID: 1316525

3

Human liver L-alanine-glyoxylate aminotransferase: characteristics and activity in controls and hyperoxaluria type I patients using a simple spectrophotometric method.

Wanders RJ, Ruiter J, van Roermund CW, Schutgens RB, Ofman R, Jurriaans S, Tager JM. Wanders RJ, et al. Clin Chim Acta. 1990 Aug 15;189(2):139-44. doi: 10.1016/0009-8981(90)90084-6. Clin Chim Acta. 1990. PMID: 2397596

4

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype.

Ijlst L, Uskikubo S, Kamijo T, Hashimoto T, Ruiter JP, de Klerk JB, Wanders RJ. Ijlst L, et al. Among authors: ruiter jp. J Inherit Metab Dis. 1995;18(2):241-4. doi: 10.1007/BF00711778. J Inherit Metab Dis. 1995. PMID: 7564258 No abstract available.

5

Inhibition of oxidative phosphorylation by palmitoyl-CoA in digitonin permeabilized fibroblasts: implications for long-chain fatty acid beta-oxidation disorders.

Ventura FV, Ruiter JP, Ijlst L, Almeida IT, Wanders RJ. Ventura FV, et al. Among authors: ruiter jp. Biochim Biophys Acta. 1995 Aug 15;1272(1):14-20. doi: 10.1016/0925-4439(95)00064-b. Biochim Biophys Acta. 1995. PMID: 7662716 Free article.

6

Differentiation and proliferation of respiration-deficient human myoblasts.

Herzberg NH, Zwart R, Wolterman RA, Ruiter JP, Wanders RJ, Bolhuis PA, van den Bogert C. Herzberg NH, et al. Among authors: ruiter jp. Biochim Biophys Acta. 1993 Mar 24;1181(1):63-7. doi: 10.1016/0925-4439(93)90091-e. Biochim Biophys Acta. 1993. PMID: 7681329

7

Mitochondrial oxidative phosphorylation in digitonin-permeabilized chorionic villus fibroblasts: a new method with potential for prenatal diagnosis.

Wanders RJ, Ruiter JP, Wijburg FA. Wanders RJ, et al. Among authors: ruiter jp. J Inherit Metab Dis. 1994;17(3):304-6. doi: 10.1007/BF00711814. J Inherit Metab Dis. 1994. PMID: 7807938 No abstract available.

8

Studies on mitochondrial oxidative phosphorylation in permeabilized human skin fibroblasts: application to mitochondrial encephalomyopathies.

Wanders RJ, Ruiter JP, Wijburg FA. Wanders RJ, et al. Among authors: ruiter jp. Biochim Biophys Acta. 1993 Jun 19;1181(3):219-22. doi: 10.1016/0925-4439(93)90024-u. Biochim Biophys Acta. 1993. PMID: 8318549

9

Prenatal diagnosis of systemic disorders of the respiratory chain in cultured chorionic villus fibroblasts by study of ATP-synthesis in digitonin-permeabilized cells.

Wanders RJ, Ruiter JP, Wijburg FA, Zeman J, Klement P, Houstek J. Wanders RJ, et al. Among authors: ruiter jp. J Inherit Metab Dis. 1996;19(2):133-6. doi: 10.1007/BF01799412. J Inherit Metab Dis. 1996. PMID: 8739948 No abstract available.

10

Inhibitory effect of 3-hydroxyacyl-CoAs and other long-chain fatty acid beta-oxidation intermediates on mitochondrial oxidative phosphorylation.

Ventura FV, Ruiter JP, Ijlst L, de Almeida IT, Wanders RJ. Ventura FV, et al. Among authors: ruiter jp. J Inherit Metab Dis. 1996;19(2):161-4. doi: 10.1007/BF01799419. J Inherit Metab Dis. 1996. PMID: 8739955 No abstract available.

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