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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

151 related items for PubMed ID: 8428062

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.
    Nakamura M, Yabe I, Sudo A, Hosoki K, Yaguchi H, Saitoh S, Sasaki H.
    J Med Genet; 2010 Oct; 47(10):659-64. PubMed ID: 20610441
    [Abstract] [Full Text] [Related]

  • 3. [MERRF/MELAS overlap syndrome].
    Goto Y.
    Ryoikibetsu Shokogun Shirizu; 2001 Oct; (36):159. PubMed ID: 11596353
    [No Abstract] [Full Text] [Related]

  • 4. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
    Seibel P, Flierl A, Kottlors M, Reichmann H.
    Biochem Biophys Res Commun; 1994 Apr 29; 200(2):938-42. PubMed ID: 8179630
    [Abstract] [Full Text] [Related]

  • 5. [MERRF/MELAS overlap syndrome].
    Goto Y.
    Nihon Rinsho; 2002 Apr 29; 60 Suppl 4():296-7. PubMed ID: 12013869
    [No Abstract] [Full Text] [Related]

  • 6. Update in molecular genetics: mitochondrial energy transduction disorders.
    Marzuki S, Sudoyo H, Lertrit P.
    Southeast Asian J Trop Med Public Health; 1995 Apr 29; 26 Suppl 1():155-61. PubMed ID: 8629096
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. mtDNA mutations confer cellular sensitivity to oxidant stress that is partially rescued by calcium depletion and cyclosporin A.
    Wong A, Cortopassi G.
    Biochem Biophys Res Commun; 1997 Oct 09; 239(1):139-45. PubMed ID: 9345284
    [Abstract] [Full Text] [Related]

  • 11. Mitochondrial encephalomyopathy associated with a novel mutation in the mitochondrial tRNA(leu)(UUR) gene (A3243T).
    Shaag A, Saada A, Steinberg A, Navon P, Elpeleg ON.
    Biochem Biophys Res Commun; 1997 Apr 28; 233(3):637-9. PubMed ID: 9168904
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Detection and quantification of point mutations in mitochondrial DNA by PCR.
    Yoneda M, Tanno Y, Tsuji S, Attardi G.
    Methods Enzymol; 1996 Apr 28; 264():432-41. PubMed ID: 8965716
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.
    Liu CS, Cheng WL, Lee CF, Ma YS, Lin CY, Huang CC, Wei YH.
    Acta Neurol Scand; 2006 May 28; 113(5):334-41. PubMed ID: 16629770
    [Abstract] [Full Text] [Related]

  • 19. Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease.
    Kirino Y, Goto Y, Campos Y, Arenas J, Suzuki T.
    Proc Natl Acad Sci U S A; 2005 May 17; 102(20):7127-32. PubMed ID: 15870203
    [Abstract] [Full Text] [Related]

  • 20. Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation.
    Yasukawa T, Suzuki T, Ishii N, Ueda T, Ohta S, Watanabe K.
    FEBS Lett; 2000 Feb 11; 467(2-3):175-8. PubMed ID: 10675533
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.