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A comprehensive review of genetic association studies.
Hirschhorn JN, Lohmueller K, Byrne E, Hirschhorn K. Hirschhorn JN, et al. Among authors: byrne e. Genet Med. 2002 Mar-Apr;4(2):45-61. doi: 10.1097/00125817-200203000-00002. Genet Med. 2002. PMID: 11882781 Review.
Normal variants of human mitochondrial DNA and translation products: the building of a reference data base.
Marzuki S, Noer AS, Lertrit P, Thyagarajan D, Kapsa R, Utthanaphol P, Byrne E. Marzuki S, et al. Among authors: byrne e. Hum Genet. 1991 Dec;88(2):139-45. doi: 10.1007/BF00206061. Hum Genet. 1991. PMID: 1757091
mtDNA in congenital myotonic dystrophy.
Thyagarajan D, Byrne E, Noer AS, Lertrit P, Kapsa R, Marzuki S. Thyagarajan D, et al. Among authors: byrne e. Am J Hum Genet. 1993 Jan;52(1):207-10. Am J Hum Genet. 1993. PMID: 8192709 Free PMC article. No abstract available.
Tissue segregation of a heteroplasmic mtDNA mutation in MERRF (myoclonic epilepsy with ragged red fibers) encephalomyopathy.
Lertrit P, Noer AS, Byrne E, Marzuki S. Lertrit P, et al. Among authors: byrne e. Hum Genet. 1992 Nov;90(3):251-4. doi: 10.1007/BF00220072. Hum Genet. 1992. PMID: 1487239
Mitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNA.
Collins S, Rudduck C, Marzuki S, Dennett X, Byrne E. Collins S, et al. Among authors: byrne e. Biochim Biophys Acta. 1991 Nov 21;1097(4):309-17. doi: 10.1016/0925-4439(91)90086-o. Biochim Biophys Acta. 1991. PMID: 1660306
Chronic progressive external ophthalmoplegia in patients with large heteroplasmic mitochondrial DNA deletions: an immunocytochemical study.
Collins S, Dennett X, Byrne E, Marzuki S. Collins S, et al. Among authors: byrne e. Acta Neuropathol. 1991;82(3):185-92. doi: 10.1007/BF00294444. Acta Neuropathol. 1991. PMID: 1656694
Reduced collagen VI causes Bethlem myopathy: a heterozygous COL6A1 nonsense mutation results in mRNA decay and functional haploinsufficiency.
Lamandé SR, Bateman JF, Hutchison W, McKinlay Gardner RJ, Bower SP, Byrne E, Dahl HH. Lamandé SR, et al. Among authors: byrne e. Hum Mol Genet. 1998 Jun;7(6):981-9. doi: 10.1093/hmg/7.6.981. Hum Mol Genet. 1998. PMID: 9580662
In vivo and in vitro correction of the mdx dystrophin gene nonsense mutation by short-fragment homologous replacement.
Kapsa R, Quigley A, Lynch GS, Steeper K, Kornberg AJ, Gregorevic P, Austin L, Byrne E. Kapsa R, et al. Among authors: byrne e. Hum Gene Ther. 2001 Apr 10;12(6):629-42. doi: 10.1089/104303401300057324. Hum Gene Ther. 2001. PMID: 11426463
Decline in skeletal muscle mitochondrial respiratory chain function: possible factor in ageing.
Trounce I, Byrne E, Marzuki S. Trounce I, et al. Among authors: byrne e. Lancet. 1989 Mar 25;1(8639):637-9. doi: 10.1016/s0140-6736(89)92143-0. Lancet. 1989. PMID: 2564459
The polymerase chain reaction in the study of mitochondrial genetics.
Kapsa R, Siregar N, Quigley A, Ojaimi J, Katsabanis S, Sue C, Byrne E. Kapsa R, et al. Among authors: byrne e. J Biochem Biophys Methods. 1997 Dec 17;36(1):31-50. doi: 10.1016/s0165-022x(97)00044-4. J Biochem Biophys Methods. 1997. PMID: 9507371
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