Jackson Christopher Benjamin: Difference between revisions
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|lastname=Jackson | |lastname=Jackson | ||
|firstname=Christopher Benjamin | |firstname=Christopher Benjamin | ||
|institution=Biomedicum Helsinki | |institution=Biomedicum Helsinki, | ||
Research Program for Molecular Neurology | Research Program for Molecular Neurology, FI | ||
|city=Helsinki | |city=Helsinki | ||
|country=Finnland | |country=Finnland |
Revision as of 16:44, 10 December 2018
Name | Jackson Christopher Benjamin, |
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Institution | Biomedicum Helsinki,
Research Program for Molecular Neurology, FI |
Address | , |
City | Helsinki |
State/Province | |
Country | Finnland |
[email protected] | |
Weblink | |
O2k-Network Lab | CH Bern Nuoffer JM |
Labels:
Publications
Published | Reference | |
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Daura 2021 Neurobiol Dis | 2021 | Daura E, Tegelberg S, Yoshihara M, Jackson C, Simonetti F, Aksentjeff K, Ezer S, Hakala P, Katayama S, Kere J, Lehesjoki AE, Joensuu T (2021) Cystatin B-deficiency triggers ectopic histone H3 tail cleavage during neurogenesis. Neurobiol Dis 156:105418. |
BEC 2020.1 doi10.26124bec2020-0001.v1 | 2020 | Gnaiger E et al β MitoEAGLE Task Group (2020) Mitochondrial physiology. Bioenerg Commun 2020.1. https://doi.org/10.26124/bec:2020-0001.v1 |
Richter 2019 Life Sci Alliance | 2019 | Richter U, Ng KY, Suomi F, Marttinen P, Turunen T, Jackson C, Suomalainen A, Vihinen H, Jokitalo E, Nyman TA, Isokallio MA, Stewart JB, Mancini C, Brusco A, Seneca S, Lombès A, Taylor RW, Battersby BJ (2019) Mitochondrial stress response triggered by defects in protein synthesis quality control. Life Sci Alliance 2:e201800219. |
Ignatenko 2018 Nat Commun | 2018 | Ignatenko O, Chilov D, Paetau I, de Miguel E, Jackson CB, Capin G, Paetau A, Terzioglu M, Euro L, Suomalainen A (2018) Loss of mtDNA activates astrocytes and leads to spongiotic encephalopathy. Nat Commun 9:70. |
Isohanni 2018 Neurogenetics | 2018 | Isohanni P, Carroll CJ, Jackson CB, Pohjanpelto M, LΓΆnnqvist T, Suomalainen A (2018) Defective mitochondrial ATPase due to rare mtDNA m.8969G>A mutation-causing lactic acidosis, intellectual disability, and poor growth. Neurogenetics 19:49-53. |
Jackson 2014 J Med Genet | 2014 | Jackson CB, Nuoffer JM, Hahn D, Prokisch H, Haberberger B, Gautsch M, HΓ€berli A, Gallati S, Schaller A (2014) Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial Complex II deficiency. J Med Genet 51:170-5. |