211 related articles for article (PubMed ID: 34257281)
21. Phosphorylation of the outer membrane mitochondrial protein OM64 influences protein import into mitochondria.
Nickel C; Horneff R; Heermann R; Neumann B; Jung K; Soll J; Schwenkert S
Mitochondrion; 2019 Jan; 44():93-102. PubMed ID: 29374544
[TBL] [Abstract][Full Text] [Related]
22. TOM70 Sustains Cell Bioenergetics by Promoting IP3R3-Mediated ER to Mitochondria Ca
Filadi R; Leal NS; Schreiner B; Rossi A; Dentoni G; Pinho CM; Wiehager B; Cieri D; Calì T; Pizzo P; Ankarcrona M
Curr Biol; 2018 Feb; 28(3):369-382.e6. PubMed ID: 29395920
[TBL] [Abstract][Full Text] [Related]
23. A biophysical analysis of the tetratricopeptide repeat-rich mitochondrial import receptor, Tom70, reveals an elongated monomer that is inherently flexible, unstable, and unfolds via a multistate pathway.
Beddoe T; Bushell SR; Perugini MA; Lithgow T; Mulhern TD; Bottomley SP; Rossjohn J
J Biol Chem; 2004 Nov; 279(45):46448-54. PubMed ID: 15316022
[TBL] [Abstract][Full Text] [Related]
24. Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A.
Bronicki LM; Redin C; Drunat S; Piton A; Lyons M; Passemard S; Baumann C; Faivre L; Thevenon J; Rivière JB; Isidor B; Gan G; Francannet C; Willems M; Gunel M; Jones JR; Gleeson JG; Mandel JL; Stevenson RE; Friez MJ; Aylsworth AS
Eur J Hum Genet; 2015 Nov; 23(11):1482-7. PubMed ID: 25920557
[TBL] [Abstract][Full Text] [Related]
25. Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.
Møller RS; Kübart S; Hoeltzenbein M; Heye B; Vogel I; Hansen CP; Menzel C; Ullmann R; Tommerup N; Ropers HH; Tümer Z; Kalscheuer VM
Am J Hum Genet; 2008 May; 82(5):1165-70. PubMed ID: 18405873
[TBL] [Abstract][Full Text] [Related]
26. Normalizing the gene dosage of Dyrk1A in a mouse model of Down syndrome rescues several Alzheimer's disease phenotypes.
García-Cerro S; Rueda N; Vidal V; Lantigua S; Martínez-Cué C
Neurobiol Dis; 2017 Oct; 106():76-88. PubMed ID: 28647555
[TBL] [Abstract][Full Text] [Related]
27. DYRK1A regulates Hap1-Dcaf7/WDR68 binding with implication for delayed growth in Down syndrome.
Xiang J; Yang S; Xin N; Gaertig MA; Reeves RH; Li S; Li XJ
Proc Natl Acad Sci U S A; 2017 Feb; 114(7):E1224-E1233. PubMed ID: 28137862
[TBL] [Abstract][Full Text] [Related]
28. tRNA import across the mitochondrial inner membrane in T. brucei requires TIM subunits but is independent of protein import.
Shikha S; Huot JL; Schneider A; Niemann M
Nucleic Acids Res; 2020 Dec; 48(21):12269-12281. PubMed ID: 33231678
[TBL] [Abstract][Full Text] [Related]
29. Tom70-based transcriptional regulation of mitochondrial biogenesis and aging.
Liu Q; Chang CE; Wooldredge AC; Fong B; Kennedy BK; Zhou C
Elife; 2022 Mar; 11():. PubMed ID: 35234609
[TBL] [Abstract][Full Text] [Related]
30. Function of cytosolic chaperones in Tom70-mediated mitochondrial import.
Fan AC; Young JC
Protein Pept Lett; 2011 Feb; 18(2):122-31. PubMed ID: 20955164
[TBL] [Abstract][Full Text] [Related]
31. Role of membrane contact sites in protein import into mitochondria.
Horvath SE; Rampelt H; Oeljeklaus S; Warscheid B; van der Laan M; Pfanner N
Protein Sci; 2015 Mar; 24(3):277-97. PubMed ID: 25514890
[TBL] [Abstract][Full Text] [Related]
32. Dual Role of Mitochondrial Porin in Metabolite Transport across the Outer Membrane and Protein Transfer to the Inner Membrane.
Ellenrieder L; Dieterle MP; Doan KN; Mårtensson CU; Floerchinger A; Campo ML; Pfanner N; Becker T
Mol Cell; 2019 Mar; 73(5):1056-1065.e7. PubMed ID: 30738704
[TBL] [Abstract][Full Text] [Related]
33. DYRK1A mutations in two unrelated patients.
Ruaud L; Mignot C; Guët A; Ohl C; Nava C; Héron D; Keren B; Depienne C; Benoit V; Maystadt I; Lederer D; Amsallem D; Piard J
Eur J Med Genet; 2015 Mar; 58(3):168-74. PubMed ID: 25641759
[TBL] [Abstract][Full Text] [Related]
34. Glucose-induced regulation of protein import receptor Tom22 by cytosolic and mitochondria-bound kinases.
Gerbeth C; Schmidt O; Rao S; Harbauer AB; Mikropoulou D; Opalińska M; Guiard B; Pfanner N; Meisinger C
Cell Metab; 2013 Oct; 18(4):578-87. PubMed ID: 24093680
[TBL] [Abstract][Full Text] [Related]
35. The Mitochondrial Import Complex MIM Functions as Main Translocase for α-Helical Outer Membrane Proteins.
Doan KN; Grevel A; Mårtensson CU; Ellenrieder L; Thornton N; Wenz LS; Opaliński Ł; Guiard B; Pfanner N; Becker T
Cell Rep; 2020 Apr; 31(4):107567. PubMed ID: 32348752
[TBL] [Abstract][Full Text] [Related]
36. The chaperone-binding activity of the mitochondrial surface receptor Tom70 protects the cytosol against mitoprotein-induced stress.
Backes S; Bykov YS; Flohr T; Räschle M; Zhou J; Lenhard S; Krämer L; Mühlhaus T; Bibi C; Jann C; Smith JD; Steinmetz LM; Rapaport D; Storchová Z; Schuldiner M; Boos F; Herrmann JM
Cell Rep; 2021 Apr; 35(1):108936. PubMed ID: 33826901
[TBL] [Abstract][Full Text] [Related]
37. Nascent mitochondrial proteins initiate the localized condensation of cytosolic protein aggregates on the mitochondrial surface.
Liu Q; Fong B; Yoo S; Unruh JR; Guo F; Yu Z; Chen J; Si K; Li R; Zhou C
Proc Natl Acad Sci U S A; 2023 Aug; 120(31):e2300475120. PubMed ID: 37494397
[TBL] [Abstract][Full Text] [Related]
38. Human mitochondrial import receptor Tom70 functions as a monomer.
Fan AC; Gava LM; Ramos CH; Young JC
Biochem J; 2010 Aug; 429(3):553-63. PubMed ID: 20504278
[TBL] [Abstract][Full Text] [Related]
39. Transgenic mouse in vivo library of human Down syndrome critical region 1: association between DYRK1A overexpression, brain development abnormalities, and cell cycle protein alteration.
Branchi I; Bichler Z; Minghetti L; Delabar JM; Malchiodi-Albedi F; Gonzalez MC; Chettouh Z; Nicolini A; Chabert C; Smith DJ; Rubin EM; Migliore-Samour D; Alleva E
J Neuropathol Exp Neurol; 2004 May; 63(5):429-40. PubMed ID: 15198122
[TBL] [Abstract][Full Text] [Related]
40. Inactivation of the Neurospora crassa mitochondrial outer membrane protein TOM70 by repeat-induced point mutation (RIP) causes defects in mitochondrial protein import and morphology.
Grad LI; Descheneau AT; Neupert W; Lill R; Nargang FE
Curr Genet; 1999 Sep; 36(3):137-46. PubMed ID: 10501936
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]