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Items: 1 to 20 of 38

1.

LEBER'S DISEASE WITH SYMPTOMS RESEMBLING DISSEMINATED SCLEROSIS.

LEES F, MACDONALD AM, TURNER JW.

J Neurol Neurosurg Psychiatry. 1964 Oct;27:415-21. No abstract available.

2.

LEBER'S DISEASE IN THE NETHERLANDS.

VANSENUS AH.

Doc Ophthalmol. 1963;17:1-162. Review. No abstract available.

PMID:
14187151
3.

A SEX-LINKED HEREDO-DEGENERATIVE NEUROLOGICAL DISORDER, ASSOCIATED WITH LEBER'S OPTIC ATROPHY. I. CLINICAL STUDIES.

BRUYN GW, WENT LN.

J Neurol Sci. 1964 Jan-Feb;1(1):59-80. No abstract available.

PMID:
14175627
4.

The mitochondnal genome of Aspergillus nidulans contains reading frames homologous to the human URFs 1 and 4.

Brown TA, Davies RW, Ray JA, Waring RB, Scazzocchio C.

EMBO J. 1983;2(3):427-35.

5.

Sequence and gene organization of mouse mitochondrial DNA.

Bibb MJ, Van Etten RA, Wright CT, Walberg MW, Clayton DA.

Cell. 1981 Oct;26(2 Pt 2):167-80.

PMID:
7332926
6.

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
7.

Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome.

Anderson S, de Bruijn MH, Coulson AR, Eperon IC, Sanger F, Young IG.

J Mol Biol. 1982 Apr 25;156(4):683-717. No abstract available.

PMID:
7120390
8.

A simple method for displaying the hydropathic character of a protein.

Kyte J, Doolittle RF.

J Mol Biol. 1982 May 5;157(1):105-32. No abstract available.

PMID:
7108955
10.

Further clinical and pathological observations on Leber's optic atrophy.

Adams JH, Blackwood W, Wilson J.

Brain. 1966 Mar;89(1):15-26. No abstract available.

PMID:
5910901
11.

The heart in Leber's optic atrophy.

Rose FC, Bowden AN, Bowden PM.

Br J Ophthalmol. 1970 Jun;54(6):388-93. No abstract available.

12.
13.

Neurological studies in families with Leber's optic atrophy.

de Weerdt CJ, Went LN.

Acta Neurol Scand. 1971;47(5):541-54. No abstract available.

PMID:
5139723
14.

The complete nucleotide sequence of the Xenopus laevis mitochondrial genome.

Roe BA, Ma DP, Wilson RK, Wong JF.

J Biol Chem. 1985 Aug 15;260(17):9759-74.

15.

The inheritance of Leber's disease. A genealogical follow-up study.

Seedorff T.

Acta Ophthalmol (Copenh). 1985 Apr;63(2):135-45.

PMID:
4003041
16.

Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase.

Chomyn A, Mariottini P, Cleeter MW, Ragan CI, Matsuno-Yagi A, Hatefi Y, Doolittle RF, Attardi G.

Nature. 1985 Apr 18-24;314(6012):592-7.

PMID:
3921850
17.

URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit.

Chomyn A, Cleeter MW, Ragan CI, Riley M, Doolittle RF, Attardi G.

Science. 1986 Oct 31;234(4776):614-8.

PMID:
3764430
18.

Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees.

Nikoskelainen EK, Savontaus ML, Wanne OP, Katila MJ, Nummelin KU.

Arch Ophthalmol. 1987 May;105(5):665-71.

PMID:
3619743
19.

Photolabelling of a mitochondrially encoded subunit of NADH dehydrogenase with [3H]dihydrorotenone.

Earley FG, Patel SD, Ragan I, Attardi G.

FEBS Lett. 1987 Jul 13;219(1):108-12.

20.

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

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