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 *

83 related articles for article (PubMed ID: 12013871)

  • 21. Mitochondrial DNA medicine.
    DiMauro S
    Biosci Rep; 2007 Jun; 27(1-3):5-9. PubMed ID: 17484047
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Current classification of mitochondrial disorders.
    Andreu AL; DiMauro S
    J Neurol; 2003 Dec; 250(12):1403-6. PubMed ID: 14673571
    [No Abstract]   [Full Text] [Related]  

  • 23. MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA.
    Taylor RW; Chinnery PF; Haldane F; Morris AA; Bindoff LA; Wilson J; Turnbull DM
    Ann Neurol; 1996 Sep; 40(3):459-62. PubMed ID: 8797538
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Identification of mutations in mtDNA from patients suffering mitochondrial diseases.
    Schon EA; Naini A; Shanske S
    Methods Mol Biol; 2002; 197():55-74. PubMed ID: 12013813
    [No Abstract]   [Full Text] [Related]  

  • 25. Lactic acidemia and mitochondrial disease.
    Robinson BH
    Mol Genet Metab; 2006; 89(1-2):3-13. PubMed ID: 16854608
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Mammalian mtDNA mutations and related disorders: overview].
    Nonaka I
    Tanpakushitsu Kakusan Koso; 2005 Nov; 50(14 Suppl):1759. PubMed ID: 16318309
    [No Abstract]   [Full Text] [Related]  

  • 27. Expanding the clinical phenotype of the mitochondrial m.13513G>A mutation with the first report of a fatal neonatal presentation: importance of DNA collection for post-mortem diagnosis.
    Gropman AL
    Dev Med Child Neurol; 2011 Jun; 53(6):487-8. PubMed ID: 21518342
    [No Abstract]   [Full Text] [Related]  

  • 28. Paternal transmission of mitochondrial DNA is (fortunately) rare.
    Johns DR
    Ann Neurol; 2003 Oct; 54(4):422-4. PubMed ID: 14520651
    [No Abstract]   [Full Text] [Related]  

  • 29. Mitochondrial functional complementation in mitochondrial DNA-based diseases.
    Nakada K; Sato A; Hayashi J
    Int J Biochem Cell Biol; 2009 Oct; 41(10):1907-13. PubMed ID: 19464386
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation.
    McFarland R; Clark KM; Morris AA; Taylor RW; Macphail S; Lightowlers RN; Turnbull DM
    Nat Genet; 2002 Feb; 30(2):145-6. PubMed ID: 11799391
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mitochondrial DNA mutations in human disease.
    DiMauro S; Schon EA
    Am J Med Genet; 2001; 106(1):18-26. PubMed ID: 11579421
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Respiratory chain complex I deficiency.
    Triepels RH; Van Den Heuvel LP; Trijbels JM; Smeitink JA
    Am J Med Genet; 2001; 106(1):37-45. PubMed ID: 11579423
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mitochondrial DNA-related disorders.
    Mancuso M; Filosto M; Choub A; Tentorio M; Broglio L; Padovani A; Siciliano G
    Biosci Rep; 2007 Jun; 27(1-3):31-7. PubMed ID: 17484046
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines.
    Bornstein B; Mas JA; Fernández-Moreno MA; Campos Y; Martín MA; del Hoyo P; Rubio JC; Arenas J; Garesse R
    Hum Mutat; 2002 Mar; 19(3):234-9. PubMed ID: 11857739
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Ptosis as an associated finding in maternally inherited diabetes and deafness.
    Robberecht K; Decock C; Stevens A; Seneca S; De Bleecker J; Leroy BP
    Ophthalmic Genet; 2010 Dec; 31(4):240-3. PubMed ID: 21067488
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mitochondrial genes and neuromuscular disease.
    Wallace DC
    Res Publ Assoc Res Nerv Ment Dis; 1991; 69():101-20. PubMed ID: 2003154
    [No Abstract]   [Full Text] [Related]  

  • 37. Oxidative phosphorylation diseases and stroke.
    Shoffner JM; Wallace DC
    Heart Dis Stroke; 1993; 2(5):439-45. PubMed ID: 8137048
    [No Abstract]   [Full Text] [Related]  

  • 38. A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intolerance.
    Mayr JA; Moslemi AR; Förster H; Kamper A; Idriceanu C; Muss W; Huemer M; Oldfors A; Sperl W
    Neuromuscul Disord; 2006 Dec; 16(12):874-7. PubMed ID: 17056256
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies.
    Hess JF; Parisi MA; Bennett JL; Clayton DA
    Nature; 1991 May; 351(6323):236-9. PubMed ID: 1755869
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Clinical features of A3243G mitochondrial tRNA mutation.
    Chae JH; Hwang H; Lim BC; Cheong HI; Hwang YS; Kim KJ
    Brain Dev; 2004 Oct; 26(7):459-62. PubMed ID: 15351082
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.