Land JM - Search Results

1

Diagnostic value of succinate ubiquinone reductase activity in the identification of patients with mitochondrial DNA depletion.

Hargreaves P, Rahman S, Guthrie P, Taanman JW, Leonard JV, Land JM, Heales SJ. Hargreaves P, et al. Among authors: land jm. J Inherit Metab Dis. 2002 Feb;25(1):7-16. doi: 10.1023/a:1015104910239. J Inherit Metab Dis. 2002. PMID: 12004863

2

Mitochondrial damage: an important feature in a number of inborn errors of metabolism?

Heales SJ, Bolaños JP, Brand MP, Clark JB, Land JM. Heales SJ, et al. Among authors: land jm. J Inherit Metab Dis. 1996;19(2):140-2. doi: 10.1007/BF01799414. J Inherit Metab Dis. 1996. PMID: 8739950 No abstract available.

3

Mitochondrial respiratory chain defects are not accompanied by an increase in the activities of lactate dehydrogenase or manganese superoxide dismutase in paediatric skeletal muscle biopsies.

Hargreaves IP, Heales SJ, Land JM. Hargreaves IP, et al. Among authors: land jm. J Inherit Metab Dis. 1999 Dec;22(8):925-31. doi: 10.1023/a:1005643508075. J Inherit Metab Dis. 1999. PMID: 10604144

4

Blood mononuclear cell coenzyme Q10 concentration and mitochondrial respiratory chain succinate cytochrome-c reductase activity in phenylketonuric patients.

Hargreaves IP, Heales SJ, Briddon A, Land JM, Lee PJ. Hargreaves IP, et al. Among authors: land jm. J Inherit Metab Dis. 2002 Dec;25(8):673-9. doi: 10.1023/a:1022881231253. J Inherit Metab Dis. 2002. PMID: 12705497 Clinical Trial.

5

Glutathione deficiency in patients with mitochondrial disease: implications for pathogenesis and treatment.

Hargreaves IP, Sheena Y, Land JM, Heales SJ. Hargreaves IP, et al. Among authors: land jm. J Inherit Metab Dis. 2005;28(1):81-8. doi: 10.1007/s10545-005-4160-1. J Inherit Metab Dis. 2005. PMID: 15702408

6

Mitochondrial cytochrome c release: a factor to consider in mitochondrial disease?

Oppenheim ML, Hargreaves IP, Pope S, Land JM, Heales SJ. Oppenheim ML, et al. Among authors: land jm. J Inherit Metab Dis. 2009 Apr;32(2):269-73. doi: 10.1007/s10545-009-1061-8. Epub 2009 Jan 26. J Inherit Metab Dis. 2009. PMID: 19169843

7

Phenotypic variability of mitochondrial disease caused by a nuclear mutation in complex II.

Pagnamenta AT, Hargreaves IP, Duncan AJ, Taanman JW, Heales SJ, Land JM, Bitner-Glindzicz M, Leonard JV, Rahman S. Pagnamenta AT, et al. Among authors: land jm. Mol Genet Metab. 2006 Nov;89(3):214-21. doi: 10.1016/j.ymgme.2006.05.003. Epub 2006 Jun 23. Mol Genet Metab. 2006. PMID: 16798039

8

Decreased ubiquinone availability and impaired mitochondrial cytochrome oxidase activity associated with statin treatment.

Duncan AJ, Hargreaves IP, Damian MS, Land JM, Heales SJ. Duncan AJ, et al. Among authors: land jm. Toxicol Mech Methods. 2009 Jan;19(1):44-50. doi: 10.1080/15376510802305047. Toxicol Mech Methods. 2009. PMID: 19778232

9

Bezafibrate induced increase in mitochondrial electron transport chain complex IV activity in human astrocytoma cells: Implications for mitochondrial cytopathies and neurodegenerative diseases.

Ioannou N, Hargreaves IP, Allen G, Duberley K, Land JM, Heales SJ. Ioannou N, et al. Among authors: land jm. Biofactors. 2010 Nov-Dec;36(6):468-73. doi: 10.1002/biof.120. Epub 2010 Sep 24. Biofactors. 2010. PMID: 20872762

10

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

Hanna MG, Nelson IP, Rahman S, Lane RJ, Land J, Heales S, Cooper MJ, Schapira AH, Morgan-Hughes JA, Wood NW. Hanna MG, et al. Am J Hum Genet. 1998 Jul;63(1):29-36. doi: 10.1086/301910. Am J Hum Genet. 1998. PMID: 9634511 Free PMC article.

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