Mitochondrial DNA marks multiple sclerosis

被引：1
|
作者：
Fyfe, Ian
机构：
[1] Nature Reviews Neurology,
来源：
NATURE REVIEWS NEUROLOGY | 2024年 / 20卷 / 04期
关键词：
D O I：
10.1038/s41582-024-00948-w
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
Mitochondrial DNA has been identified as a potential biomarker of multiple sclerosis disease activity and treatment response.
引用
收藏
页码：203 / 203
页数：1
相关论文
共 50 条
  • [31] Mitochondrial DNA deletions accumulate in the brain related to aging but not to the pathology of multiple sclerosis
    Kalman, Bernadette
    Blokhin, Andrei
    Vyshkina, Tamara
    NEUROLOGY, 2008, 70 (11) : A274 - A274
  • [32] Mitochondrial DNA Variation and Heteroplasmy in Monozygotic Twins Clinically Discordant for Multiple Sclerosis
    Souren, Nicole Y. P.
    Gerdes, Lisa A.
    Kuempfel, Tania
    Lutsik, Pavlo
    Klopstock, Thomas
    Hohlfeld, Reinhard
    Walter, Joern
    HUMAN MUTATION, 2016, 37 (08) : 765 - 775
  • [33] NO ASSOCIATION OF THE 11778-MITOCHONDRIAL-DNA MUTATION AND MULTIPLE-SCLEROSIS IN JAPAN
    NISHIMURA, M
    OBAYASHI, H
    OHTA, M
    UCHIYAMA, T
    HAO, Q
    SAIDA, T
    NEUROLOGY, 1995, 45 (07) : 1333 - 1334
  • [34] Clonally expanded mitochondrial DNA deletions within the choroid plexus in multiple sclerosis
    Campbell, Graham R.
    Kraytsberg, Yevgenya
    Krishnan, Kim J.
    Ohno, Nobuhiko
    Ziabreva, Iryna
    Reeve, Amy
    Trapp, Bruce D.
    Newcombe, Jia
    Reynolds, Richard
    Lassmann, Hans
    Khrapko, Konstantin
    Turnbull, Doug M.
    Mahad, Don J.
    ACTA NEUROPATHOLOGICA, 2012, 124 (02) : 209 - 220
  • [35] Association of common mitochondrial DNA variants with multiple sclerosis and systemic lupus erythematosus
    Vyshkina, Tamara
    Sylvester, Andrew
    Sadiq, Saud
    Bonilla, Eduardo
    Canter, Jeff A.
    Perl, Andras
    Kalman, Bernadette
    CLINICAL IMMUNOLOGY, 2008, 129 (01) : 31 - 35
  • [36] Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis
    Mojon, DS
    Herbert, J
    Sadiq, SA
    Miller, JR
    Hirano, M
    VISION RESEARCH, 1996, 36 : 3237 - 3237
  • [37] Human mitochondrial DNA and nuclear DNA isolation from food bite marks
    Zapico, Sara C.
    Menendez, Sofia T.
    ARCHIVES OF ORAL BIOLOGY, 2016, 70 : 67 - 72
  • [38] Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations.
    Pénisson-Besnier, I
    Moreau, C
    Jacques, C
    Roger, JC
    Dubas, F
    Reynier, P
    REVUE NEUROLOGIQUE, 2001, 157 (05) : 537 - 541
  • [39] A novel mitochondrial DNA deletion producing progressive external ophthalmoplegia associated with multiple sclerosis
    Slee, M.
    Finkemeyer, J.
    Krupa, M.
    Raghupathi, R.
    Gardner, J.
    Blumbergs, P.
    Agzarian, M.
    Thyagarajan, D.
    JOURNAL OF CLINICAL NEUROSCIENCE, 2011, 18 (10) : 1318 - 1324
  • [40] LEBERS HEREDITARY OPTIC NEUROPATHY MITOCHONDRIAL-DNA MUTATIONS IN MULTIPLE-SCLEROSIS
    KELLARWOOD, H
    ROBERTSON, N
    GOVAN, GG
    COMPSTON, DAS
    HARDING, AE
    ANNALS OF NEUROLOGY, 1994, 36 (01) : 109 - 112
12345