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Year | Number of Results |
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2019 | 1 |
2020 | 3 |
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2024 | 2 |
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Page 1
Activity-dependent mitochondrial ROS signaling regulates recruitment of glutamate receptors to synapses.
Elife. 2024 Mar 14;13:e92376. doi: 10.7554/eLife.92376.
Elife. 2024.
PMID: 38483244
Free PMC article.
Subcellular Imaging of Neuronal Calcium Handling In Vivo.
Doser R, Knight KM, Deihl E, Hoerndli F.
Doser R, et al. Among authors: knight km.
J Vis Exp. 2023 Mar 17;(193):10.3791/64928. doi: 10.3791/64928.
J Vis Exp. 2023.
PMID: 37010315
Free PMC article.
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Pathogenic variants in MRPL44 cause infantile cardiomyopathy due to a mitochondrial translation defect.
Friederich MW, Geddes GC, Wortmann SB, Punnoose A, Wartchow E, Knight KM, Prokisch H, Creadon-Swindell G, Mayr JA, Van Hove JLK.
Friederich MW, et al. Among authors: knight km.
Mol Genet Metab. 2021 Aug;133(4):362-371. doi: 10.1016/j.ymgme.2021.06.001. Epub 2021 Jun 10.
Mol Genet Metab. 2021.
PMID: 34140213
Free PMC article.
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A novel acceptor stem variant in mitochondrial tRNATyr impairs mitochondrial translation and is associated with a severe phenotype.
Kripps KA, Friederich MW, Chen T, Larson AA, Mirsky DM, Wang Y, Tanji K, Knight KM, Wong LJ, Van Hove JLK.
Kripps KA, et al. Among authors: knight km.
Mol Genet Metab. 2020 Dec;131(4):398-404. doi: 10.1016/j.ymgme.2020.11.006. Epub 2020 Nov 24.
Mol Genet Metab. 2020.
PMID: 33279411
Free PMC article.
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The mitochondrial DNA variant m.9032T > C in MT-ATP6 encoding p.(Leu169Pro) causes a complex mitochondrial neurological syndrome.
Knight KM, Shelkowitz E, Larson AA, Mirsky DM, Wang Y, Chen T, Wong LJ, Friederich MW, Van Hove JLK.
Knight KM, et al.
Mitochondrion. 2020 Nov;55:8-13. doi: 10.1016/j.mito.2020.08.009. Epub 2020 Sep 12.
Mitochondrion. 2020.
PMID: 32931937
Free PMC article.
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A Necessary Role for PKC-2 and TPA-1 in Olfactory Memory and Synaptic AMPAR Trafficking in Caenorhabditis elegans.
Stetak AL, Grenal T, Lenninger Z, Knight KM, Doser RL, Hoerndli FJ.
Stetak AL, et al. Among authors: knight km.
J Neurosci. 2024 Mar 6;44(10):e1120232024. doi: 10.1523/JNEUROSCI.1120-23.2024.
J Neurosci. 2024.
PMID: 38238075
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Pathogenic variants in NUBPL result in failure to assemble the matrix arm of complex I and cause a complex leukoencephalopathy with thalamic involvement.
Friederich MW, Perez FA, Knight KM, Van Hove RA, Yang SP, Saneto RP, Van Hove JLK.
Friederich MW, et al. Among authors: knight km.
Mol Genet Metab. 2020 Mar;129(3):236-242. doi: 10.1016/j.ymgme.2019.12.013. Epub 2019 Dec 30.
Mol Genet Metab. 2020.
PMID: 31917109
Free PMC article.
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