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Transgenic Research|January 22, 2021
TT2020 meeting report on the 16th Transgenic Technology MeetingReetta Hinttala, Satu KuureBMJ Case Reports|July 11, 2012
Novel POLG1 mutations in a patient with adult-onset progressive external ophthalmoplegia and encephalopathyMika H Martikainen, Reetta Hinttala, Kari MajamaaMolecular Neurodegeneration|February 26, 2010
Mitochondrial DNA haplogroups in early-onset Alzheimer's disease and frontotemporal lobar degenerationJohanna Krüger, Reetta Hinttala, Kari Majamaa, et al.Plos One|August 24, 2018
Structural analysis of human NHLRC2, mutations of which are associated with FINCA diseaseEkaterina Biterova, Alexander Ignatyev, Johanna Uusimaa, et al.Respiratory Research|August 13, 2022
NHLRC2 expression is increased in idiopathic pulmonary fibrosisMervi Kreus, Siri Lehtonen, Reetta Hinttala, et al.BMC Neurology|May 20, 2017
Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorderLaura Kytövuori, Mikko Kärppä, Hannu Tuominen, et al.Mitochondrion|May 26, 2016
Evaluating clinical mitochondrial respiratory chain enzymes from biopsy specimens presenting skewed probability distribution of activity dataMilla-Riikka Hautakangas, Reetta Hinttala, Heikki Rantala, et al.Journal of Molecular Medicine (Berlin, Germany)|September 6, 2005
Sequence analysis of nuclear genes encoding functionally important complex I subunits in children with encephalomyopathyReetta Hinttala, Johanna Uusimaa, Anne M Remes, et al.Neuroepidemiology|March 2, 2012
Progressive external ophthalmoplegia in southwestern Finland: a clinical and genetic studyMika H Martikainen, Reetta Hinttala, Matias Röyttä, et al.Genesis (New York, N.Y. : 2000)|March 8, 2022
Nhlrc2 is crucial during mouse gastrulationAnniina E Hiltunen, Reetta Vuolteenaho, Veli-Pekka Ronkainen, et al.Pageof 6