Morgan-Hughes JA - Search Results

1

Mitochondrial myopathy with a defect of mitochondrial-protein transport.

Schapira AH, Cooper JM, Morgan-Hughes JA, Landon DN, Clark JB. Schapira AH, et al. N Engl J Med. 1990 Jul 5;323(1):37-42. doi: 10.1056/NEJM199007053230107. N Engl J Med. 1990. PMID: 2113185 Free article. No abstract available.

2

Biochemical and molecular aspects of human mitochondrial respiratory chain disorders.

Cooper JM, Schapira AH, Holt IJ, Toscano A, Harding AE, Morgan-Hughes JA, Clark JB. Cooper JM, et al. Biochem Soc Trans. 1990 Aug;18(4):517-9. doi: 10.1042/bst0180517. Biochem Soc Trans. 1990. PMID: 2177405 No abstract available.

3

Human mitochondrial respiratory chain deficiencies.

Morgan-Hughes JA, Schapira AH, Cooper JM, Hayes DJ, Clark JB. Morgan-Hughes JA, et al. Aust Paediatr J. 1988;24 Suppl 1:55-7. Aust Paediatr J. 1988. PMID: 2849394 Review.

4

Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency.

Schapira AH, Cooper JM, Morgan-Hughes JA, Patel SD, Cleeter MJ, Ragan CI, Clark JB. Schapira AH, et al. Lancet. 1988 Mar 5;1(8584):500-3. doi: 10.1016/s0140-6736(88)91296-2. Lancet. 1988. PMID: 2893919

5

A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity.

Morgan-Hughes JA, Darveniza P, Landon DN, Land JM, Clark JB. Morgan-Hughes JA, et al. J Neurol Sci. 1979 Sep;43(1):27-46. doi: 10.1016/0022-510x(79)90071-6. J Neurol Sci. 1979. PMID: 521828

6

Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathy.

Hammans SR, Sweeney MG, Holt IJ, Cooper JM, Toscano A, Clark JB, Morgan-Hughes JA, Harding AE. Hammans SR, et al. J Neurol Sci. 1992 Jan;107(1):87-92. doi: 10.1016/0022-510x(92)90213-5. J Neurol Sci. 1992. PMID: 1315844

7

One-step immunoaffinity purification of complex I subunits from beef heart mitochondria.

Haines AM, Cooper JM, Morgan-Hughes JA, Clark JB, Schapira AH. Haines AM, et al. Protein Expr Purif. 1992 Jun;3(3):223-7. doi: 10.1016/1046-5928(92)90018-r. Protein Expr Purif. 1992. PMID: 1392618

8

Treatment of experimental NADH ubiquinone reductase deficiency with menadione.

Cooper JM, Hayes DJ, Challiss RA, Morgan-Hughes JA, Clark JB. Cooper JM, et al. Brain. 1992 Aug;115 ( Pt 4):991-1000. Brain. 1992. PMID: 1393515

9

The molecular pathology of human respiratory chain defects.

Morgan-Hughes JA, Cooper JM, Schapira AH, Sweeny M, Holt IJ, Harding AE, Clark JB. Morgan-Hughes JA, et al. Rev Neurol (Paris). 1991;147(6-7):450-4. Rev Neurol (Paris). 1991. PMID: 1962049 Review.

10

The molecular pathology of respiratory-chain dysfunction in human mitochondrial myopathies.

Morgan-Hughes JA, Schapira AH, Cooper JM, Holt IJ, Harding AE, Clark JB. Morgan-Hughes JA, et al. Biochim Biophys Acta. 1990 Jul 25;1018(2-3):217-22. doi: 10.1016/0005-2728(90)90252-y. Biochim Biophys Acta. 1990. PMID: 2168209

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