These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
207 related articles for article (PubMed ID: 26486469)
1. A canine orthologue of the human GFAP c.716G>A (p.Arg239His) variant causes Alexander disease in a Labrador retriever. Van Poucke M; Martlé V; Van Brantegem L; Ducatelle R; Van Ham L; Bhatti S; Peelman LJ Eur J Hum Genet; 2016 Jun; 24(6):852-6. PubMed ID: 26486469 [TBL] [Abstract][Full Text] [Related]
2. GFAP variants leading to infantile Alexander disease: Phenotype and genotype analysis of 135 cases and report of a de novo variant. Heshmatzad K; Haghi Panah M; Tavasoli AR; Ashrafi MR; Mahdieh N; Rabbani B Clin Neurol Neurosurg; 2021 Aug; 207():106754. PubMed ID: 34146839 [TBL] [Abstract][Full Text] [Related]
3. Aggregation-prone GFAP mutation in Alexander disease validated using a zebrafish model. Lee SH; Nam TS; Kim KH; Kim JH; Yoon W; Heo SH; Kim MJ; Shin BA; Perng MD; Choy HE; Jo J; Kim MK; Choi SY BMC Neurol; 2017 Sep; 17(1):175. PubMed ID: 28882119 [TBL] [Abstract][Full Text] [Related]
4. The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and the association of alpha B-crystallin and HSP27. Der Perng M; Su M; Wen SF; Li R; Gibbon T; Prescott AR; Brenner M; Quinlan RA Am J Hum Genet; 2006 Aug; 79(2):197-213. PubMed ID: 16826512 [TBL] [Abstract][Full Text] [Related]
5. Screening for GFAP rearrangements in a cohort of Alexander disease and undetermined leukoencephalopathy patients. Ferreira MC; Dorboz I; Rodriguez D; Boespflug Tanguy O Eur J Med Genet; 2015 Sep; 58(9):466-70. PubMed ID: 26208460 [TBL] [Abstract][Full Text] [Related]
6. The origin of Rosenthal fibers and their contributions to astrocyte pathology in Alexander disease. Sosunov AA; McKhann GM; Goldman JE Acta Neuropathol Commun; 2017 Mar; 5(1):27. PubMed ID: 28359321 [TBL] [Abstract][Full Text] [Related]
7. Synemin is expressed in reactive astrocytes and Rosenthal fibers in Alexander disease. Pekny T; Faiz M; Wilhelmsson U; Curtis MA; Matej R; Skalli O; Pekny M APMIS; 2014 Jan; 122(1):76-80. PubMed ID: 23594359 [TBL] [Abstract][Full Text] [Related]
8. Alexander disease-associated glial fibrillary acidic protein mutations in mice induce Rosenthal fiber formation and a white matter stress response. Hagemann TL; Connor JX; Messing A J Neurosci; 2006 Oct; 26(43):11162-73. PubMed ID: 17065456 [TBL] [Abstract][Full Text] [Related]
9. Neonatal Alexander Disease: Novel GFAP Mutation and Comparison to Previously Published Cases. Knuutinen O; Kousi M; Suo-Palosaari M; Moilanen JS; Tuominen H; Vainionpää L; Joensuu T; Anttonen AK; Uusimaa J; Lehesjoki AE; Vieira P Neuropediatrics; 2018 Aug; 49(4):256-261. PubMed ID: 29801191 [TBL] [Abstract][Full Text] [Related]
10. Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing. Heshmatzad K; Naderi N; Masoumi T; Pouraliakbar H; Kalayinia S Eur J Med Res; 2022 Sep; 27(1):174. PubMed ID: 36088400 [TBL] [Abstract][Full Text] [Related]
11. Aggregate formation analysis of GFAP Tulyeu J; Tamaura M; Jimbo E; Shimbo H; Takano K; Iai M; Yamashita S; Goto T; Aida N; Tokuhiro E; Yamagata T; Osaka H Brain Dev; 2019 Feb; 41(2):195-200. PubMed ID: 30213442 [TBL] [Abstract][Full Text] [Related]
12. Glial fibrillary acidic protein is pathologically modified in Alexander disease. Lin NH; Jian WS; Snider N; Perng MD J Biol Chem; 2024 Jul; 300(7):107402. PubMed ID: 38782207 [TBL] [Abstract][Full Text] [Related]
13. GFAP mutations in Alexander disease. Li R; Messing A; Goldman JE; Brenner M Int J Dev Neurosci; 2002; 20(3-5):259-68. PubMed ID: 12175861 [TBL] [Abstract][Full Text] [Related]
14. A case of severe Alexander disease with de novo c. 239 T > C, p.(F80S), in GFAP. Matsumoto A; Tulyeu J; Furukawa R; Watanabe C; Monden Y; Nozaki Y; Mori M; Namekawa M; Jimbo EF; Aihara T; Yamagata T; Osaka H Brain Dev; 2018 Aug; 40(7):587-591. PubMed ID: 29573842 [TBL] [Abstract][Full Text] [Related]
15. Clinical and genetic study in Chinese patients with Alexander disease. Ye Wu ; Qiang Gu ; Jingmin Wang ; Yanling Yang ; Xiru Wu ; Yuwu Jiang J Child Neurol; 2008 Feb; 23(2):173-7. PubMed ID: 18079314 [TBL] [Abstract][Full Text] [Related]
16. Plectin regulates the organization of glial fibrillary acidic protein in Alexander disease. Tian R; Gregor M; Wiche G; Goldman JE Am J Pathol; 2006 Mar; 168(3):888-97. PubMed ID: 16507904 [TBL] [Abstract][Full Text] [Related]
17. Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease. Li R; Johnson AB; Salomons G; Goldman JE; Naidu S; Quinlan R; Cree B; Ruyle SZ; Banwell B; D'Hooghe M; Siebert JR; Rolf CM; Cox H; Reddy A; Gutiérrez-Solana LG; Collins A; Weller RO; Messing A; van der Knaap MS; Brenner M Ann Neurol; 2005 Mar; 57(3):310-26. PubMed ID: 15732097 [TBL] [Abstract][Full Text] [Related]
18. Follow-up study of 22 Chinese children with Alexander disease and analysis of parental origin of de novo GFAP mutations. Zang L; Wang J; Jiang Y; Gu Q; Gao Z; Yang Y; Xiao J; Wu Y J Hum Genet; 2013 Apr; 58(4):183-8. PubMed ID: 23364391 [TBL] [Abstract][Full Text] [Related]
19. Clinical aspects and pathology of Alexander disease, and morphological and functional alteration of astrocytes induced by GFAP mutation. Yoshida T; Nakagawa M Neuropathology; 2012 Aug; 32(4):440-6. PubMed ID: 22118268 [TBL] [Abstract][Full Text] [Related]
20. Glial fibrillary acidic protein exhibits altered turnover kinetics in a mouse model of Alexander disease. Moody LR; Barrett-Wilt GA; Sussman MR; Messing A J Biol Chem; 2017 Apr; 292(14):5814-5824. PubMed ID: 28223355 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]