| Year |
Citation |
Score |
| 2023 |
Konovalova S, Torregrosa-Muñumer R, Manjunath P, Liu X, Baral S, Fatima K, Holopainen M, Kvist J, Rajendran J, Yang Y, Varjosalo M, Käkelä R, Somerharju P, Tyynismaa H. Small mitochondrial protein NERCLIN regulates cardiolipin homeostasis and mitochondrial ultrastructure. Proceedings of the National Academy of Sciences of the United States of America. 120: e2210599120. PMID 37463214 DOI: 10.1073/pnas.2210599120 |
0.635 |
|
| 2022 |
Döhla J, Kuuluvainen E, Gebert N, Amaral A, Englund JI, Gopalakrishnan S, Konovalova S, Nieminen AI, Salminen ES, Torregrosa Muñumer R, Ahlqvist K, Yang Y, Bui H, Otonkoski T, Käkelä R, et al. Metabolic determination of cell fate through selective inheritance of mitochondria. Nature Cell Biology. 24: 148-154. PMID 35165416 DOI: 10.1038/s41556-021-00837-0 |
0.328 |
|
| 2020 |
Harjuhaahto S, Rasila TS, Molchanova SM, Woldegebriel R, Kvist J, Konovalova S, Sainio MT, Pennonen J, Torregrosa-Muñumer R, Ibrahim H, Otonkoski T, Taira T, Ylikallio E, Tyynismaa H. ALS and Parkinson's disease genes CHCHD10 and CHCHD2 modify synaptic transcriptomes in human iPSC-derived motor neurons. Neurobiology of Disease. 141: 104940. PMID 32437855 DOI: 10.1016/J.Nbd.2020.104940 |
0.32 |
|
| 2020 |
Nevanlinna V, Konovalova S, Ceulemans B, Muona M, Laari A, Hilander T, Gorski K, Valanne L, Anttonen AK, Tyynismaa H, Courage C, Lehesjoki AE. A patient with pontocerebellar hypoplasia type 6: Novel RARS2 mutations, comparison to previously published patients and clinical distinction from PEHO syndrome. European Journal of Medical Genetics. 63: 103766. PMID 31536827 DOI: 10.1016/J.Ejmg.2019.103766 |
0.333 |
|
| 2019 |
Konovalova S. Analysis of Mitochondrial Respiratory Chain Complexes in Cultured Human Cells using Blue Native Polyacrylamide Gel Electrophoresis and Immunoblotting. Journal of Visualized Experiments : Jove. PMID 30829336 DOI: 10.3791/59269 |
0.449 |
|
| 2018 |
Sommerville EW, Zhou XL, Oláhová M, Jenkins J, Euro L, Konovalova S, Hilander T, Pyle A, He L, Habeebu S, Saunders C, Kelsey A, Morris AAM, McFarland R, Suomalainen A, et al. Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy. Human Molecular Genetics. PMID 30285085 DOI: 10.1093/Hmg/Ddy294 |
0.438 |
|
| 2018 |
Konovalova S, Liu X, Manjunath P, Baral S, Neupane N, Hilander T, Yang Y, Balboa D, Terzioglu M, Euro L, Varjosalo M, Tyynismaa H. Redox regulation of GRPEL2 nucleotide exchange factor for mitochondrial HSP70 chaperone. Redox Biology. 19: 37-45. PMID 30098457 DOI: 10.1016/J.Redox.2018.07.024 |
0.605 |
|
| 2018 |
Hilander T, Konovalova S, Terzioglu M, Tyynismaa H. Analysis of Mitochondrial Protein Synthesis: De Novo Translation, Steady-State Levels, and Assembled OXPHOS Complexes. Current Protocols in Toxicology. e56. PMID 30063298 DOI: 10.1002/Cptx.56 |
0.583 |
|
| 2018 |
Hilander T, Zhou XL, Konovalova S, Zhang FP, Euro L, Chilov D, Poutanen M, Chihade J, Wang ED, Tyynismaa H. Editing activity for eliminating mischarged tRNAs is essential in mammalian mitochondria. Nucleic Acids Research. 46: 849-860. PMID 29228266 DOI: 10.1093/Nar/Gkx1231 |
0.565 |
|
| 2016 |
Agalakova NI, Brailovskaya IV, Konovalova SA, Korotkov SM, Lavrova EA, Nikiforov AA. ATP-consuming processes in hepatocytes of river lamprey Lampetra fluviatilis on the course of prespawning starvation. Comparative Biochemistry and Physiology. Part a, Molecular & Integrative Physiology. 201: 95-100. PMID 27399971 DOI: 10.1016/j.cbpa.2016.07.002 |
0.318 |
|
| 2015 |
Ylikallio E, Konovalova S, Dhungana Y, Hilander T, Junna N, Partanen JV, Toppila JP, Auranen M, Tyynismaa H. Truncated HSPB1 causes axonal neuropathy and impairs tolerance to unfolded protein stress. Bba Clinical. 3: 233-42. PMID 26675522 DOI: 10.1016/J.Bbacli.2015.03.002 |
0.429 |
|
| 2015 |
Konovalova S, Hilander T, Loayza-Puch F, Rooijers K, Agami R, Tyynismaa H. Exposure to arginine analog canavanine induces aberrant mitochondrial translation products, mitoribosome stalling, and instability of the mitochondrial proteome. The International Journal of Biochemistry & Cell Biology. 65: 268-74. PMID 26117454 DOI: 10.1016/J.Biocel.2015.06.018 |
0.583 |
|
| 2015 |
Euro L, Konovalova S, Asin-Cayuela J, Tulinius M, Griffin H, Horvath R, Taylor RW, Chinnery PF, Schara U, Thorburn DR, Suomalainen A, Chihade J, Tyynismaa H. Structural modeling of tissue-specific mitochondrial alanyl-tRNA synthetase (AARS2) defects predicts differential effects on aminoacylation. Frontiers in Genetics. 6: 21. PMID 25705216 DOI: 10.3389/Fgene.2015.00021 |
0.465 |
|
| 2014 |
Zaitsev BN, Benedetti F, Mikhaylov AG, Korneev DV, Sekatskii SK, Karakouz T, Belavin PA, Netesova NA, Protopopova EV, Konovalova SN, Dietler G, Loktev VB. Force-induced globule-coil transition in laminin binding protein and its role for viral-cell membrane fusion. Journal of Molecular Recognition : Jmr. 27: 727-38. PMID 25319621 DOI: 10.1002/jmr.2399 |
0.363 |
|
| 2014 |
Ylikallio E, Johari M, Konovalova S, Moilanen JS, Kiuru-Enari S, Auranen M, Pajunen L, Tyynismaa H. Targeted next-generation sequencing reveals further genetic heterogeneity in axonal Charcot-Marie-Tooth neuropathy and a mutation in HSPB1. European Journal of Human Genetics : Ejhg. 22: 522-7. PMID 23963299 DOI: 10.1038/Ejhg.2013.190 |
0.302 |
|
| 2013 |
Konovalova S, Tyynismaa H. Mitochondrial aminoacyl-tRNA synthetases in human disease. Molecular Genetics and Metabolism. 108: 206-11. PMID 23433712 DOI: 10.1016/J.Ymgme.2013.01.010 |
0.473 |
|
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