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Items: 1 to 20 of 42

1.

Sequence and organization of the human mitochondrial genome.

Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJ, Staden R, Young IG.

Nature. 1981 Apr 9;290(5806):457-65.

PMID:
7219534
2.

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.

Pavlakis SG, Phillips PC, DiMauro S, De Vivo DC, Rowland LP.

Ann Neurol. 1984 Oct;16(4):481-8.

PMID:
6093682
3.

The Kearns-Shy syndrome. A multisystem disease with mitochondrial abnormality demonstrated in skeletal muscle and skin.

Karpati G, Carpenter S, Larbrisseau A, Lafontaine R.

J Neurol Sci. 1973 Jun;19(2):133-51. No abstract available.

PMID:
4712930
4.

Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.

Olson W, Engel WK, Walsh GO, Einaugler R.

Arch Neurol. 1972 Mar;26(3):193-211. No abstract available.

PMID:
4400816
5.
6.

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ 2nd, Nikoskelainen EK.

Science. 1988 Dec 9;242(4884):1427-30.

PMID:
3201231
7.

Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency.

Koga Y, Nonaka I, Kobayashi M, Tojyo M, Nihei K.

Ann Neurol. 1988 Dec;24(6):749-56.

PMID:
3144939
9.

Priming of human mitochondrial DNA replication occurs at the light-strand promoter.

Chang DD, Clayton DA.

Proc Natl Acad Sci U S A. 1985 Jan;82(2):351-5.

10.

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.

Holt IJ, Harding AE, Morgan-Hughes JA.

Nature. 1988 Feb 25;331(6158):717-9.

PMID:
2830540
11.

Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.

Nelson I, Degoul F, Obermaier-Kusser B, Romero N, Borrone C, Marsac C, Vayssiere JL, Gerbitz K, Fardeau M, Ponsot G, Lestienne P.

Nucleic Acids Res. 1989 Oct 25;17(20):8117-24.

13.

Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA.

Holt IJ, Harding AE, Cooper JM, Schapira AH, Toscano A, Clark JB, Morgan-Hughes JA.

Ann Neurol. 1989 Dec;26(6):699-708.

PMID:
2604380
14.

Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.

Mita S, Schmidt B, Schon EA, DiMauro S, Bonilla E.

Proc Natl Acad Sci U S A. 1989 Dec;86(23):9509-13.

15.

Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscle.

Romero NB, Lestienne P, Marsac C, Paturneau-Jouas M, Nelson I, Fran├žois D, Eymard B, Fardeau M.

J Neurol Sci. 1989 Nov;93(2-3):297-309.

PMID:
2556504
16.

Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: neuropathology, biochemistry, and molecular genetics.

Lombes A, Mendell JR, Nakase H, Barohn RJ, Bonilla E, Zeviani M, Yates AJ, Omerza J, Gales TL, Nakahara K, et al.

Ann Neurol. 1989 Jul;26(1):20-33.

PMID:
2549843
17.

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.

Moraes CT, DiMauro S, Zeviani M, Lombes A, Shanske S, Miranda AF, Nakase H, Bonilla E, Werneck LC, Servidei S, et al.

N Engl J Med. 1989 May 18;320(20):1293-9.

PMID:
2541333
18.

Shedding light on PCR contamination.

Sarkar G, Sommer SS.

Nature. 1990 Jan 4;343(6253):27. No abstract available.

PMID:
2296286
19.

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

Kobayashi Y, Momoi MY, Tominaga K, Momoi T, Nihei K, Yanagisawa M, Kagawa Y, Ohta S.

Biochem Biophys Res Commun. 1990 Dec 31;173(3):816-22.

PMID:
2268345
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