231 related articles for article (PubMed ID: 19091982)
21. A survival pathway for Caenorhabditis elegans with a blocked unfolded protein response.
Urano F; Calfon M; Yoneda T; Yun C; Kiraly M; Clark SG; Ron D
J Cell Biol; 2002 Aug; 158(4):639-46. PubMed ID: 12186849
[TBL] [Abstract][Full Text] [Related]
22. WDR45 contributes to neurodegeneration through regulation of ER homeostasis and neuronal death.
Wan H; Wang Q; Chen X; Zeng Q; Shao Y; Fang H; Liao X; Li HS; Liu MG; Xu TL; Diao M; Li D; Meng B; Tang B; Zhang Z; Liao L
Autophagy; 2020 Mar; 16(3):531-547. PubMed ID: 31204559
[TBL] [Abstract][Full Text] [Related]
23. Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1.
Du J; Hu YC; Tang BS; Chen C; Luo YY; Zhan ZX; Zhao GH; Jiang H; Xia K; Shen L
Clin Neurol Neurosurg; 2011 Jul; 113(6):480-2. PubMed ID: 21419568
[TBL] [Abstract][Full Text] [Related]
24. Protrudin regulates endoplasmic reticulum morphology and function associated with the pathogenesis of hereditary spastic paraplegia.
Hashimoto Y; Shirane M; Matsuzaki F; Saita S; Ohnishi T; Nakayama KI
J Biol Chem; 2014 May; 289(19):12946-61. PubMed ID: 24668814
[TBL] [Abstract][Full Text] [Related]
25. Hereditary spastic paraplegia-linked REEP1 modulates endoplasmic reticulum/mitochondria contacts.
Lim Y; Cho IT; Schoel LJ; Cho G; Golden JA
Ann Neurol; 2015 Nov; 78(5):679-96. PubMed ID: 26201691
[TBL] [Abstract][Full Text] [Related]
26. Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese families.
Chen S; Song C; Guo H; Xu P; Huang W; Zhou Y; Sun J; Li CX; Du Y; Li X; Liu Z; Geng D; Maxwell PH; Zhang C; Wang Y
Hum Mutat; 2005 Feb; 25(2):135-41. PubMed ID: 15643603
[TBL] [Abstract][Full Text] [Related]
27. Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots.
Beetz C; Schüle R; Klebe S; Klimpe S; Klopstock T; Lacour A; Otto S; Sperfeld AD; van de Warrenburg B; Schöls L; Deufel T
J Neurol Sci; 2008 May; 268(1-2):131-5. PubMed ID: 18191948
[TBL] [Abstract][Full Text] [Related]
28. Rescue of ATXN3 neuronal toxicity in
Fardghassemi Y; Tauffenberger A; Gosselin S; Parker JA
Dis Model Mech; 2017 Dec; 10(12):1465-1480. PubMed ID: 29061563
[TBL] [Abstract][Full Text] [Related]
29. Clinical and Genetic Features of Chinese Patients With
Fu J; Ma M; Li G; Zhang J
Front Genet; 2022; 13():859688. PubMed ID: 35464835
[No Abstract] [Full Text] [Related]
30. Modeling of axonal endoplasmic reticulum network by spastic paraplegia proteins.
Yalçın B; Zhao L; Stofanko M; O'Sullivan NC; Kang ZH; Roost A; Thomas MR; Zaessinger S; Blard O; Patto AL; Sohail A; Baena V; Terasaki M; O'Kane CJ
Elife; 2017 Jul; 6():. PubMed ID: 28742022
[TBL] [Abstract][Full Text] [Related]
31. Neuronal toxicity in Caenorhabditis elegans from an editing site mutant in glutamate receptor channels.
Aronoff R; Mellem JE; Maricq AV; Sprengel R; Seeburg PH
J Neurosci; 2004 Sep; 24(37):8135-40. PubMed ID: 15371514
[TBL] [Abstract][Full Text] [Related]
32. ER-shaping proteins are required for ER and mitochondrial network organization in motor neurons.
Fowler PC; O'Sullivan NC
Hum Mol Genet; 2016 Jul; 25(13):2827-2837. PubMed ID: 27170313
[TBL] [Abstract][Full Text] [Related]
33. Liver X receptor-agonist treatment rescues degeneration in a Drosophila model of hereditary spastic paraplegia.
Byrne DJ; Garcia-Pardo ME; Cole NB; Batnasan B; Heneghan S; Sohail A; Blackstone C; O'Sullivan NC
Acta Neuropathol Commun; 2022 Mar; 10(1):40. PubMed ID: 35346366
[TBL] [Abstract][Full Text] [Related]
34. A spastic paraplegia mouse model reveals REEP1-dependent ER shaping.
Beetz C; Koch N; Khundadze M; Zimmer G; Nietzsche S; Hertel N; Huebner AK; Mumtaz R; Schweizer M; Dirren E; Karle KN; Irintchev A; Alvarez V; Redies C; Westermann M; Kurth I; Deufel T; Kessels MM; Qualmann B; Hübner CA
J Clin Invest; 2013 Oct; 123(10):4273-82. PubMed ID: 24051375
[TBL] [Abstract][Full Text] [Related]
35. Mutant spastin proteins promote deficits in axonal transport through an isoform-specific mechanism involving casein kinase 2 activation.
Leo L; Weissmann C; Burns M; Kang M; Song Y; Qiang L; Brady ST; Baas PW; Morfini G
Hum Mol Genet; 2017 Jun; 26(12):2321-2334. PubMed ID: 28398512
[TBL] [Abstract][Full Text] [Related]
36. ER Morphology in the Pathogenesis of Hereditary Spastic Paraplegia.
Sonda S; Pendin D; Daga A
Cells; 2021 Oct; 10(11):. PubMed ID: 34831093
[TBL] [Abstract][Full Text] [Related]
37. The Caenorhabditis elegans HP1 family protein HPL-2 maintains ER homeostasis through the UPR and hormesis.
Kozlowski L; Garvis S; Bedet C; Palladino F
Proc Natl Acad Sci U S A; 2014 Apr; 111(16):5956-61. PubMed ID: 24715729
[TBL] [Abstract][Full Text] [Related]
38. Epilepsy in hereditary spastic paraplegia associated with NIPA1 gene.
Boysen S; Elumalai V; ElSheikh RH; Aravindhan A; Veerapandiyan A
J Clin Neurosci; 2022 Jun; 100():212-213. PubMed ID: 35181192
[No Abstract] [Full Text] [Related]
39. The effects of ER morphology on synaptic structure and function in Drosophila melanogaster.
Summerville JB; Faust JF; Fan E; Pendin D; Daga A; Formella J; Stern M; McNew JA
J Cell Sci; 2016 Apr; 129(8):1635-48. PubMed ID: 26906425
[TBL] [Abstract][Full Text] [Related]
40. MANF deletion abrogates early larval Caenorhabditis elegans stress response to tunicamycin and Pseudomonas aeruginosa.
Hartman JH; Richie CT; Gordon KL; Mello DF; Castillo P; Zhu A; Wang Y; Hoffer BJ; Sherwood DR; Meyer JN; Harvey BK
Eur J Cell Biol; 2019 Dec; 98(5-8):151043. PubMed ID: 31138438
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]