From Bioblast
O2k-Publications: Autism
Sort in ascending/descending order by a click on one of the small symbols in squares below. Default sorting: chronological. Empty fields appear first in ascending order.
Year | Reference | Organism | Tissue;cell | |
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Rydzanicz 2024 EMBO Mol Med | 2024 | Rydzanicz M, Kuzniewska B, Magnowska M, WΓ³jtowicz T, Stawikowska A, Hojka A, Borsuk E, Meyza K, Gewartowska O, Gruchota J, MiΕek J, Wardaszka P, Chojnicka I, Kondrakiewicz L, Dymkowska D, PuΕcian A, Knapska E, Dziembowski A, PΕoski R, Dziembowska M (2024) Mutation in the mitochondrial chaperone TRAP1 leads to autism with more severe symptoms in males. EMBO Mol Med [Epub ahead of print]. https://doi.org/10.1038/s44321-024-00147-6 | Mouse | Nervous system |
Pochakom 2022 Brain Sci | 2022 | Pochakom A, Mu C, Rho JM, Tompkins TA, Mayengbam S, Shearer J (2022) Selective probiotic treatment positively modulates the microbiota-gut-brain axis in the BTBR mouse model of autism. https://doi.org/10.3390/brainsci12060781 | Mouse | Nervous system |
Abdel-Rahman 2021 Free Radic Res | 2021 | Abdel-Rahman EA, Zaky EA, Aboulsaoud M, Elhossiny RM, Youssef WY, Mahmoud AM, Ali SS (2021) Autism spectrum disorder (ASD)-associated mitochondrial deficits are revealed in children's platelets but unimproved by hyperbaric oxygen therapy. Free Radic Res 55:26-40. | ||
Yardeni 2021 Proc Natl Acad Sci U S A | 2021 | Yardeni T, Cristancho AG, McCoy AJ, Schaefer PM, McManus MJ, Marsh ED, Wallace DC (2021) An mtDNA mutant mouse demonstrates that mitochondrial deficiency can result in autism endophenotypes. Proc Natl Acad Sci U S A 118:e2021429118. | Mouse | Nervous system |
Vandenberg 2021 Neurochem Int | 2021 | Vandenberg GG, Dawson NJ, Head A, Scott GR, Scott AL (2021) Astrocyte-mediated disruption of ROS homeostasis in Fragile X mouse model. Neurochem Int 146:105036. | Mouse | Nervous system |
Hassan 2020 MitoFit Preprint Arch | 2020 | Hassan Hazirah, Gnaiger Erich, Zakaria Fazaine, Makpol Suzana, Abdul Karim Norwahidah (2020) Alterations in mitochondrial respiratory capacity and membrane potential: a link between mitochondrial dysregulation and autism. MitoFit Preprint Arch 2020.3. https://doi.org/10.26124/mitofit:200003 | Human | |
Weisz 2018 Hum Mol Genet | 2018 | Weisz ED, Towheed A, Monyak RE, Toth MS, Wallace DC, Jongens TA (2018) Loss of Drosophila FMRP leads to alterations in energy metabolism and mitochondrial function. Hum Mol Genet 27:95-106. | Drosophila | Skeletal muscle |
O2k-Publications: Autism - Abstracts
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Year | Reference | Organism | Tissue;cell | |
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Marelsson 2011 Abstract IOC61 | 2011 | Marelsson S (2011) Mitochondrial dysfunction in children with unknown encephalopathy. MiPNet16.01. | Human | Blood cells Fibroblast |