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  • 1
    ISSN: 1432-1459
    Keywords: Cluster headache ; Mitochondrial DNA ; Point mutations ; MELAS syndrome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Various mutations in the mitochondrial tRNALeu(UUR) gene give rise to a variety of neurological disorders. Among these, mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS syndrome) are frequently associated with a tRNALeu(UUR) mutation at nucleotide position 3243 of the mitochondrial DNA. A supplementary clinical feature seen in these patients is headache in early life. Recently, a tRNALeu(UUR) mutation at nucleotide position 3243 has been found in a patient presenting with cluster headache. This led us to examine the mitochondrial genomes of 22 patients presenting with cluster headache. None of the patients harboured the reported tRNALeu(UUR) mutation or any other length variations of the mtDNA. Cluster headache is most likely not causally associated with the A3243G mutation of the mitochondrial DNA.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular and cellular biochemistry 174 (1997), S. 271-275 
    ISSN: 1573-4919
    Keywords: multiple symmetric lipomatosis ; mitochondrial DNA ; MERRF
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Multiple symmetric lipomatosis (MSL) is a rare disorder of middle life characterized by large subcutaneous fat masses around the neck, shoulders and other parts of the trunk. Peripheral neuropathy is a common finding in these predominantly male patients. Employing electrophysiological measures, we found additional signs of central nervous system involvement in a majority of patients. Etiologically, there is an association with mitochondrial dysfunction. In muscle biopsy, we found ragged red fibers in 8 of 12 patients. Molecular genetic analysis revealed multiple deletions of mitochondrial DNA in one patient and the MERRF mutation at nucleotide 8344 in another. In this review, we summarize our clinical, electrophysiological morphological, biochemical and molecular genetic findings in 17 MSL patients, and give a survey of the literature. (Mol Cell Biochem 174: 271–275, 1997)
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 30 (1996), S. 235-243 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Genetic variations of the mitochondrial genome lead to severe neuromuscular diseases in man. A treatment of these utilizing a somatic gene therapy approach is invariably linked to a mitochondrial transfection system. A novel technique of targeting nucleic acids to mitochondria has been developed that takes advantage of the protein import pathway. The system is based on chimerical molecules that are composed of a DNA and a protein moiety, harboring the information for mitochondrial targeting. Upon recognition of these molecules by a receptor on the outer mitochondrial membrane, the molecules are able to cross the membrane system and are released into the matrix of the organelle. The further development of this technique will give to rise to strategies for the treatment of mitochondrial DNA diseases by a somatic gene therapy approach.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Book
    Book
    [Berkeley, Calif.] :Apress [u.a.],
    Title: Coders at work
    Author: Seibel, Peter
    Publisher: [Berkeley, Calif.] :Apress [u.a.],
    Year of publication: 2009
    Pages: XIII, 617 S.
    ISBN: 1-430-21948-3 , 978-1-430-21948-4 , 978-1-4302-1949-1
    Type of Medium: Book
    Language: English
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