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Biochimica Et Biophysica Acta|February 21, 1992
Antipeptide antibodies to the carboxy terminal and the DCCD binding region of the human mitochondrial ATP synthase beta-subunitA S Noer, S Marzuki, W S AllisonHuman Genetics|November 1, 1992
Tissue segregation of a heteroplasmic mtDNA mutation in MERRF (myoclonic epilepsy with ragged red fibers) encephalomyopathyP Lertrit, A S Noer, E Byrne, et al.Biochemistry International|May 1, 1989
The association of the autoantigens of primary biliary cirrhosis with the mitochondrial H+-ATPase--a reassessmentH Sudoyo, A S Noer, I R Mackay, et al.Acta Neurologica Scandinavica|January 1, 1993
Significance of mitochondrial DNA deletions in myotonic dystrophyD Thyagarajan, E Byrne, S Noer, et al.Annals of Neurology|November 1, 1991
Mitochondrial DNA sequence analysis in congenital myotonic dystrophyD Thyagarajan, E Byrne, S Noer, et al.Human Genetics|December 1, 1991
Normal variants of human mitochondrial DNA and translation products: the building of a reference data baseS Marzuki, A S Noer, P Lertrit, et al.American Journal of Human Genetics|October 1, 1991
A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndromeA S Noer, H Sudoyo, P Lertrit, et al.Human Molecular Genetics|November 1, 1994
Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunctionP Lertrit, R M Kapsa, M J Jean-Francois, et al.Beneficial Microbes|February 19, 2020
Lactobacillus plantarum IS-10506 promotes renal tubular regeneration in pyelonephritic ratsR V Prasetyo, I Surono, N A Soemyarso, et al.American Journal of Human Genetics|September 1, 1992
A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex IP Lertrit, A S Noer, M J Jean-Francois, et al.Pageof 2