These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 7573056)

  • 21. Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.
    Brown MD; Torroni A; Huoponen K; Chen YS; Lott MT; Wallace DC
    Am J Hum Genet; 1994 Aug; 55(2):410-2. PubMed ID: 8037217
    [No Abstract]   [Full Text] [Related]  

  • 22. Quantification of point mutations associated with Leber hereditary optic neuroretinopathy by solid-phase minisequencing.
    Juvonen V; Huoponen K; Syvänen AC; Nikoskelainen E; Savontaus ML
    Hum Genet; 1994 Jan; 93(1):16-20. PubMed ID: 8270249
    [TBL] [Abstract][Full Text] [Related]  

  • 23. High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy.
    Mashima Y; Hiida Y; Oguchi Y; Kudoh J; Shimizu N
    Hum Genet; 1993 Aug; 92(1):101-2. PubMed ID: 8103501
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cytochrome c oxidase mutations in Leber hereditary optic neuropathy.
    Johns DR; Neufeld MJ
    Biochem Biophys Res Commun; 1993 Oct; 196(2):810-5. PubMed ID: 8240356
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
    Chinnery PF; Brown DT; Andrews RM; Singh-Kler R; Riordan-Eva P; Lindley J; Applegarth DA; Turnbull DM; Howell N
    Brain; 2001 Jan; 124(Pt 1):209-18. PubMed ID: 11133798
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.
    Mackey DA; Oostra RJ; Rosenberg T; Nikoskelainen E; Bronte-Stewart J; Poulton J; Harding AE; Govan G; Bolhuis PA; Norby S
    Am J Hum Genet; 1996 Aug; 59(2):481-5. PubMed ID: 8755941
    [No Abstract]   [Full Text] [Related]  

  • 27. Leber hereditary optic neuropathy.
    Sadun AA; Sadun F
    Ophthalmology; 1996 Feb; 103(2):201-2. PubMed ID: 8594500
    [No Abstract]   [Full Text] [Related]  

  • 28. mtDNA mutations in Leber's hereditary optic neuropathy.
    Savontaus ML
    Biochim Biophys Acta; 1995 May; 1271(1):261-3. PubMed ID: 7599218
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Three subgroups of patients from the United Kingdom with Leber hereditary optic neuropathy.
    Mackey DA
    Eye (Lond); 1994; 8 ( Pt 4)():431-6. PubMed ID: 7821467
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Association of the LHON 13,708 and 15,257 mitochondrial DNA mutations with neurodegenerative diseases distinct from LHON.
    Rödel G; Laubhan R; Scheuerle A; Skowronek P; Haferkamp O
    Eur J Med Res; 1996 Jul; 1(10):491-4. PubMed ID: 9438147
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Leber's hereditary optic neuropathy. Clinical manifestations of the 15257 mutation.
    Johns DR; Smith KH; Savino PJ; Miller NR
    Ophthalmology; 1993 Jul; 100(7):981-6. PubMed ID: 8321540
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations.
    Nikoskelainen EK; Huoponen K; Juvonen V; Lamminen T; Nummelin K; Savontaus ML
    Ophthalmology; 1996 Mar; 103(3):504-14. PubMed ID: 8600429
    [TBL] [Abstract][Full Text] [Related]  

  • 33. mtDNA mutations that cause optic neuropathy: how do we know?
    Howell N; Bogolin C; Jamieson R; Marenda DR; Mackey DA
    Am J Hum Genet; 1998 Jan; 62(1):196-202. PubMed ID: 9443868
    [No Abstract]   [Full Text] [Related]  

  • 34. An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
    Johns DR; Neufeld MJ; Park RD
    Biochem Biophys Res Commun; 1992 Sep; 187(3):1551-7. PubMed ID: 1417830
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.
    Harding AE; Sweeney MG; Govan GG; Riordan-Eva P
    Am J Hum Genet; 1995 Jul; 57(1):77-86. PubMed ID: 7611298
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.
    Obermaier-Kusser B; Lorenz B; Schubring S; Paprotta A; Zerres K; Meitinger T; Meire F; Cochaux P; Blankenagel A; Kommerell G
    Am J Hum Genet; 1994 Nov; 55(5):1063-6. PubMed ID: 7977345
    [No Abstract]   [Full Text] [Related]  

  • 37. [Leber's optic nerve atrophy; a mitochondrial hereditary disease].
    Oostra RJ; Bolhuis PA; Wijburg FA; Bleeker-Wagemakers EM
    Ned Tijdschr Geneeskd; 1995 Jul; 139(26):1327-31. PubMed ID: 7617050
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Neuromyelitis optica (Devic's syndrome): no association with the primary mitochondrial DNA mutations found in Leber hereditary optic neuropathy.
    Cock H; Mandler R; Ahmed W; Schapira AH
    J Neurol Neurosurg Psychiatry; 1997 Jan; 62(1):85-7. PubMed ID: 9010406
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy.
    Torroni A; Carelli V; Petrozzi M; Terracina M; Barboni P; Malpassi P; Wallace DC; Scozzari R
    Am J Hum Genet; 1996 Jul; 59(1):248-52. PubMed ID: 8659531
    [No Abstract]   [Full Text] [Related]  

  • 40. An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene.
    Howell N; McCullough D
    Am J Hum Genet; 1990 Oct; 47(4):629-34. PubMed ID: 2121024
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.