408 related articles for article (PubMed ID: 28158749)
1. ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia.
Cooper HM; Yang Y; Ylikallio E; Khairullin R; Woldegebriel R; Lin KL; Euro L; Palin E; Wolf A; Trokovic R; Isohanni P; Kaakkola S; Auranen M; Lönnqvist T; Wanrooij S; Tyynismaa H
Hum Mol Genet; 2017 Apr; 26(8):1432-1443. PubMed ID: 28158749
[TBL] [Abstract][Full Text] [Related]
2. Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes.
Harel T; Yoon WH; Garone C; Gu S; Coban-Akdemir Z; Eldomery MK; Posey JE; Jhangiani SN; Rosenfeld JA; Cho MT; Fox S; Withers M; Brooks SM; Chiang T; Duraine L; Erdin S; Yuan B; Shao Y; Moussallem E; Lamperti C; Donati MA; Smith JD; McLaughlin HM; Eng CM; Walkiewicz M; Xia F; Pippucci T; Magini P; Seri M; Zeviani M; Hirano M; Hunter JV; Srour M; Zanigni S; Lewis RA; Muzny DM; Lotze TE; Boerwinkle E; ; ; Gibbs RA; Hickey SE; Graham BH; Yang Y; Buhas D; Martin DM; Potocki L; Graziano C; Bellen HJ; Lupski JR
Am J Hum Genet; 2016 Oct; 99(4):831-845. PubMed ID: 27640307
[TBL] [Abstract][Full Text] [Related]
3. Functional interpretation of ATAD3A variants in neuro-mitochondrial phenotypes.
Yap ZY; Park YH; Wortmann SB; Gunning AC; Ezer S; Lee S; Duraine L; Wilichowski E; Wilson K; Mayr JA; Wagner M; Li H; Kini U; Black ED; Monaghan KG; Lupski JR; Ellard S; Westphal DS; Harel T; Yoon WH
Genome Med; 2021 Apr; 13(1):55. PubMed ID: 33845882
[TBL] [Abstract][Full Text] [Related]
4. "ATAD3C regulates ATAD3A assembly and function in the mitochondrial membrane".
Gaudó P; de Tomás-Mateo E; Garrido-Pérez N; Santana A; Ruiz-Pesini E; Montoya J; Bayona-Bafaluy P
Free Radic Biol Med; 2024 Feb; 211():114-126. PubMed ID: 38092275
[TBL] [Abstract][Full Text] [Related]
5. Mitochondrial ATAD3A combines with GRP78 to regulate the WASF3 metastasis-promoting protein.
Teng Y; Ren X; Li H; Shull A; Kim J; Cowell JK
Oncogene; 2016 Jan; 35(3):333-43. PubMed ID: 25823022
[TBL] [Abstract][Full Text] [Related]
6. Novel ATAD3A recessive mutation associated to fatal cerebellar hypoplasia with multiorgan involvement and mitochondrial structural abnormalities.
Peralta S; González-Quintana A; Ybarra M; Delmiro A; Pérez-Pérez R; Docampo J; Arenas J; Blázquez A; Ugalde C; Martín MA
Mol Genet Metab; 2019 Dec; 128(4):452-462. PubMed ID: 31727539
[TBL] [Abstract][Full Text] [Related]
7. Mitochondrial dysfunction caused by novel ATAD3A mutations.
Dorison N; Gaignard P; Bayot A; Gelot A; Becker PH; Fourati S; Lebigot E; Charles P; Wai T; Therond P; Slama A
Mol Genet Metab; 2020; 131(1-2):107-113. PubMed ID: 32933822
[TBL] [Abstract][Full Text] [Related]
8. Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia.
Koppen M; Metodiev MD; Casari G; Rugarli EI; Langer T
Mol Cell Biol; 2007 Jan; 27(2):758-67. PubMed ID: 17101804
[TBL] [Abstract][Full Text] [Related]
9. Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases.
Pierson TM; Adams D; Bonn F; Martinelli P; Cherukuri PF; Teer JK; Hansen NF; Cruz P; Mullikin For The Nisc Comparative Sequencing Program JC; Blakesley RW; Golas G; Kwan J; Sandler A; Fuentes Fajardo K; Markello T; Tifft C; Blackstone C; Rugarli EI; Langer T; Gahl WA; Toro C
PLoS Genet; 2011 Oct; 7(10):e1002325. PubMed ID: 22022284
[TBL] [Abstract][Full Text] [Related]
10. The AAA+ ATPase ATAD3A controls mitochondrial dynamics at the interface of the inner and outer membranes.
Gilquin B; Taillebourg E; Cherradi N; Hubstenberger A; Gay O; Merle N; Assard N; Fauvarque MO; Tomohiro S; Kuge O; Baudier J
Mol Cell Biol; 2010 Apr; 30(8):1984-96. PubMed ID: 20154147
[TBL] [Abstract][Full Text] [Related]
11. Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78).
Estrada-Cuzcano A; Martin S; Chamova T; Synofzik M; Timmann D; Holemans T; Andreeva A; Reichbauer J; De Rycke R; Chang DI; van Veen S; Samuel J; Schöls L; Pöppel T; Mollerup Sørensen D; Asselbergh B; Klein C; Zuchner S; Jordanova A; Vangheluwe P; Tournev I; Schüle R
Brain; 2017 Feb; 140(2):287-305. PubMed ID: 28137957
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial protein ATPase family, AAA domain containing 3A correlates with radioresistance in glioblastoma.
You WC; Chiou SH; Huang CY; Chiang SF; Yang CL; Sudhakar JN; Lin TY; Chiang IP; Shen CC; Cheng WY; Lin JC; Shieh SH; Chow KC
Neuro Oncol; 2013 Oct; 15(10):1342-52. PubMed ID: 24057885
[TBL] [Abstract][Full Text] [Related]
13. ATAD3A has a scaffolding role regulating mitochondria inner membrane structure and protein assembly.
Arguello T; Peralta S; Antonicka H; Gaidosh G; Diaz F; Tu YT; Garcia S; Shiekhattar R; Barrientos A; Moraes CT
Cell Rep; 2021 Dec; 37(12):110139. PubMed ID: 34936866
[TBL] [Abstract][Full Text] [Related]
14. The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria.
Nolden M; Ehses S; Koppen M; Bernacchia A; Rugarli EI; Langer T
Cell; 2005 Oct; 123(2):277-89. PubMed ID: 16239145
[TBL] [Abstract][Full Text] [Related]
15. Deletion of ATAD3A inhibits osteogenesis by impairing mitochondria structure and function in pre-osteoblast.
Lee H; Kim DW
Dev Dyn; 2022 Dec; 251(12):1982-2000. PubMed ID: 36000457
[TBL] [Abstract][Full Text] [Related]
16. Translating m-AAA protease function in mitochondria to hereditary spastic paraplegia.
Rugarli EI; Langer T
Trends Mol Med; 2006 Jun; 12(6):262-9. PubMed ID: 16647881
[TBL] [Abstract][Full Text] [Related]
17. Mitochondrial nucleoid trafficking regulated by the inner-membrane AAA-ATPase ATAD3A modulates respiratory complex formation.
Ishihara T; Ban-Ishihara R; Ota A; Ishihara N
Proc Natl Acad Sci U S A; 2022 Nov; 119(47):e2210730119. PubMed ID: 36383603
[TBL] [Abstract][Full Text] [Related]
18. Impaired mitochondrial dynamics underlie axonal defects in hereditary spastic paraplegias.
Denton K; Mou Y; Xu CC; Shah D; Chang J; Blackstone C; Li XJ
Hum Mol Genet; 2018 Jul; 27(14):2517-2530. PubMed ID: 29726929
[TBL] [Abstract][Full Text] [Related]
19. Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A.
Lepelley A; Della Mina E; Van Nieuwenhove E; Waumans L; Fraitag S; Rice GI; Dhir A; Frémond ML; Rodero MP; Seabra L; Carter E; Bodemer C; Buhas D; Callewaert B; de Lonlay P; De Somer L; Dyment DA; Faes F; Grove L; Holden S; Hully M; Kurian MA; McMillan HJ; Suetens K; Tyynismaa H; Chhun S; Wai T; Wouters C; Bader-Meunier B; Crow YJ
J Exp Med; 2021 Oct; 218(10):. PubMed ID: 34387651
[TBL] [Abstract][Full Text] [Related]
20. Human papillomavirus infection and expression of ATPase family AAA domain containing 3A, a novel anti-autophagy factor, in uterine cervical cancer.
Chen TC; Hung YC; Lin TY; Chang HW; Chiang IP; Chen YY; Chow KC
Int J Mol Med; 2011 Nov; 28(5):689-96. PubMed ID: 21743956
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
