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 *

198 related articles for article (PubMed ID: 2067633)

  • 21. Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease.
    Shoubridge EA; Karpati G; Hastings KE
    Cell; 1990 Jul; 62(1):43-9. PubMed ID: 2163769
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M; Mita S; Sakuta R; Nonaka I; Araki S
    Ann Neurol; 1993 Mar; 33(3):275-80. PubMed ID: 7684581
    [TBL] [Abstract][Full Text] [Related]  

  • 23. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.
    Zeviani M; Servidei S; Gellera C; Bertini E; DiMauro S; DiDonato S
    Nature; 1989 May; 339(6222):309-11. PubMed ID: 2725645
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy.
    Cormier V; Rotig A; Tardieu M; Colonna M; Saudubray JM; Munnich A
    Am J Hum Genet; 1991 Apr; 48(4):643-8. PubMed ID: 2014791
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size.
    Gellerich FN; Deschauer M; Chen Y; Müller T; Neudecker S; Zierz S
    Biochim Biophys Acta; 2002 Oct; 1556(1):41-52. PubMed ID: 12351217
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mitochondrial DNA deletions in mitochondrial cytopathies: observations in 19 patients.
    Yamamoto M; Clemens PR; Engel AG
    Neurology; 1991 Nov; 41(11):1822-8. PubMed ID: 1682853
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Biochemical and genetic studies in a family with mitochondrial myopathy.
    Heiman-Patterson TD; Argov Z; Chavin JM; Kalman B; Alder H; DiMauro S; Bank W; Tahmoush AJ
    Muscle Nerve; 1997 Oct; 20(10):1219-24. PubMed ID: 9324076
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardation.
    Tabaku M; Legius E; Robberecht W; Sciot R; Fryns JP; Cassiman JJ; Matthijs G
    Genet Couns; 1999; 10(3):285-93. PubMed ID: 10546101
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.
    Suomalainen A; Majander A; Wallin M; Setälä K; Kontula K; Leinonen H; Salmi T; Paetau A; Haltia M; Valanne L; Lonnqvist J; Peltonen L; Somer H
    Neurology; 1997 May; 48(5):1244-53. PubMed ID: 9153451
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathies.
    Andreetta F; Tritschler HJ; Schon EA; DiMauro S; Bonilla E
    J Neurol Sci; 1991 Sep; 105(1):88-92. PubMed ID: 1665507
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Enzyme activity analyses along ragged-red and normal single muscle fibres.
    Reichmann H
    Histochemistry; 1992 Sep; 98(2):131-4. PubMed ID: 1330995
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Disorders associated with multiple deletions of mitochondrial DNA.
    Haltia M; Suomalainen A; Majander A; Somer H
    Brain Pathol; 1992 Apr; 2(2):133-9. PubMed ID: 1341954
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mitochondrial encephalomyopathies: biochemical approach.
    Dimauro S; Moraes CT; Shanske S; Lombes A; Nakase H; Mita S; Tritschler HJ; Bonilla E; Miranda AF; Schon EA
    Rev Neurol (Paris); 1991; 147(6-7):443-9. PubMed ID: 1660180
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies].
    Laforêt P; Eymard B; Danan C; Chevallay M; Rouche A; Frachon P; Fardeau M; Lombès A
    Rev Neurol (Paris); 1997 Feb; 153(1):51-8. PubMed ID: 9296156
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndrome.
    Shanske S; Tang Y; Hirano M; Nishigaki Y; Tanji K; Bonilla E; Sue C; Krishna S; Carlo JR; Willner J; Schon EA; DiMauro S
    Am J Hum Genet; 2002 Sep; 71(3):679-83. PubMed ID: 12152148
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Specific amplification of deleted mitochondrial DNA from a myopathic patient and analysis of deleted region with S1 nuclease.
    Tanaka-Yamamoto T; Tanaka M; Ohno K; Sato W; Horai S; Ozawa T
    Biochim Biophys Acta; 1989 Nov; 1009(2):151-5. PubMed ID: 2804078
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cytochrome c oxidase deficiency.
    DiMauro S; Lombes A; Nakase H; Mita S; Fabrizi GM; Tritschler HJ; Bonilla E; Miranda AF; DeVivo DC; Schon EA
    Pediatr Res; 1990 Nov; 28(5):536-41. PubMed ID: 2175026
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non-invasive diagnosis of mitochondrial myopathy.
    Poulton J; Deadman ME; Turnbull DM; Lake B; Gardiner RM
    Clin Genet; 1991 Jan; 39(1):33-8. PubMed ID: 1997213
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mitochondrial DNA deletions in inherited recurrent myoglobinuria.
    Ohno K; Tanaka M; Sahashi K; Ibi T; Sato W; Yamamoto T; Takahashi A; Ozawa T
    Ann Neurol; 1991 Apr; 29(4):364-9. PubMed ID: 1929207
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Direct sequencing of deleted mitochondrial DNA in myopathic patients.
    Tanaka M; Sato W; Ohno K; Yamamoto T; Ozawa T
    Biochem Biophys Res Commun; 1989 Oct; 164(1):156-63. PubMed ID: 2803291
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.