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Biochemical and Biophysical Research Communications|April 29, 1994
A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathiesP Seibel, A Flierl, M Kottlors, et al.The Journal of Biological Chemistry|October 27, 1997
Pathophysiology of the MELAS 3243 transition mutationA Flierl, H Reichmann, P SeibelNeurology|May 1, 1994
Multiple symmetric lipomatosis: abnormalities in complex IV and multiple deletions in mitochondrial DNAT Klopstock, M Naumann, B Schalke, et al.Neuromuscular Disorders : NMD|July 1, 1995
Sarcoid myopathy and mitochondrial respiratory chain defects: clinicopathological, biochemical and molecular biological analysesH Reichmann, B Schalke, P Seibel, et al.Journal of Neurology|April 1, 1996
Investigation on the mitochondrial transfer RNA(Leu)(UUR) in blood cells from patients with cluster headacheP Seibel, T Grünewald, A Gundolla, et al.American Journal of Medical Genetics|April 24, 1996
VACTERL with the mitochondrial np 3243 point mutationM S Damian, P Seibel, W Schachenmayr, et al.Nucleic Acids Research|January 11, 1995
Transfection of mitochondria: strategy towards a gene therapy of mitochondrial DNA diseasesP Seibel, J Trappe, G Villani, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|May 3, 2003
Targeted delivery of DNA to the mitochondrial compartment via import sequence-conjugated peptide nucleic acidA Flierl, C Jackson, B Cottrell, et al.Biochemical and Biophysical Research Communications|October 28, 1994
Chronic progressive external ophthalmoplegia is associated with a novel mutation in the mitochondrial tRNA(Asn) geneP Seibel, J Lauber, T Klopstock, et al.Pageof 31