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topic_facet:"NADH Dehydrogenase"
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PubPharm (23)
1
Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation
enthalten in:
Journal of biomedical science
| 2023
von
Wang, J.
|
Ji, Y.
|
Ai, C.
| +5
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2
Leber's hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagy
enthalten in:
Human molecular genetics
| 2022
von
Liang, M.
|
Ji, Y.
|
Zhang, L.
| +6
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3
Mitochondrial tRNA variants in 811 Chinese probands with Leber's hereditary optic neuropathy
enthalten in:
Mitochondrion
| 2022
von
Ji, Y.
|
Zhang, J.
|
Liang, M.
| +5
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4
Assocation Between Leber's Hereditary Optic Neuropathy and MT-ND1 3460G>A Mutation-Induced Alterations in Mitochondrial Function, Apoptosis, and Mitophagy
enthalten in:
Investigative ophthalmology & visual science
| 2021
von
Zhang, J.
|
Ji, Y.
|
Chen, J.
| +7
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5
Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations
enthalten in:
Investigative ophthalmology & visual science
| 2021
von
Jin, X.
|
Zhang, J.
|
Yi, Q.
| +7
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6
Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy
enthalten in:
The Journal of biological chemistry
| 2020
von
Ji, Y.
|
Zhang, J.
|
Lu, Y.
| +9
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7
Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy
enthalten in:
Human molecular genetics
| 2019
von
Ji, Y.
|
Zhang, J.
|
Yu, J.
| +18
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8
Mitochondrial haplogroup D4j specific variant m.11696G > a(MT-ND4) may increase the penetrance and expressivity of the LHON-associated m.11778G > a mutation in Chinese pedigrees
enthalten in:
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis
| 2017
von
Xie, S.
|
Zhang, J.
|
Sun, J.
| +9
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9
The role of MT-ND1 m.3635G>A mutation in Leber's hereditary optic neuropathy
enthalten in:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
| 2016
von
Zhang, J.
|
Zhang, Z.
|
Fu, R.
| +5
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10
Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy
enthalten in:
Investigative ophthalmology & visual science
| 2016
von
Ji, Y.
|
Liang, M.
|
Zhang, J.
| +11
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Thema: NADH Dehydrogenase
Medienart
23
Aufsätze
20
E-Artikel
20
E-Ressourcen
3
Gedruckte Aufsätze
Zeitschriftentitel
7
Investigative ophthalmology & visual science
3
Human molecular genetics
2
Biochemical and biophysical research communicat...
2
Mitochondrion
2
Molecular genetics and metabolism
1
Journal of biomedical science
1
Journal of human genetics
1
Mitochondrial DNA. Part A, DNA mapping, sequenc...
1
Ophthalmology
1
The Journal of biological chemistry
1
Yi chuan = Hereditas
1
Zhonghua yi xue yi chuan xue za zhi = Zhonghua ...
Alle anzeigen ...
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Thema
23
EC 1.6.99.3
23
Journal Article
NADH Dehydrogenase
18
Research Support, Non-U.S. Gov't
17
DNA, Mitochondrial
7
NADH dehydrogenase subunit 1, human
7
NADH dehydrogenase subunit 4
6
MT-ND6 protein, human
6
Research Support, N.I.H., Extramural
5
EC 7.1.1.2
4
8L70Q75FXE
4
Adenosine Triphosphate
4
Leber's hereditary optic neuropathy
4
Multicenter Study
3
MT-ND1 protein, human
3
mitochondrial DNA
2
EC 6.1.1.1
2
Electron Transport Complex I
2
Leber’s hereditary optic neuropathy
2
Mitochondrial Proteins
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Erscheinungszeitraum
6
2020-
15
2010-2019
2
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
21
Englisch
2
Chinesisch
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