Reactome | Klopstock, T

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created	[InstanceEdit:5657574] Jupe, Steve, 2014-12-15
dbId	5657586
displayName	Klopstock, T
firstname	Thomas
initial	T
publications	[LiteratureReference:8868768] Overexpression of the mitochondrial methyltransferase TFB1M in the mouse does not impact mitoribosomal methylation status or hearing [LiteratureReference:5657576] High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease [LiteratureReference:6787419] MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention [LiteratureReference:9832377] Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant Mice [LiteratureReference:9856701] Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia [LiteratureReference:9916618] Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement [LiteratureReference:8956303] The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations
schemaClass	Person
surname	Klopstock

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