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.
211 related articles for article (PubMed ID: 37698160)
1. Friedreich's ataxia: new insights. Krasilnikova MM; Humphries CL; Shinsky EM Emerg Top Life Sci; 2023 Dec; 7(3):313-323. PubMed ID: 37698160 [TBL] [Abstract][Full Text] [Related]
2. A GAA repeat expansion reporter model of Friedreich's ataxia recapitulates the genomic context and allows rapid screening of therapeutic compounds. Lufino MM; Silva AM; Németh AH; Alegre-Abarrategui J; Russell AJ; Wade-Martins R Hum Mol Genet; 2013 Dec; 22(25):5173-87. PubMed ID: 23943791 [TBL] [Abstract][Full Text] [Related]
3. A novel GAA-repeat-expansion-based mouse model of Friedreich's ataxia. Anjomani Virmouni S; Ezzatizadeh V; Sandi C; Sandi M; Al-Mahdawi S; Chutake Y; Pook MA Dis Model Mech; 2015 Mar; 8(3):225-35. PubMed ID: 25681319 [TBL] [Abstract][Full Text] [Related]
4. Generation and characterization of iPSC lines from Friedreich's ataxia patient (FRDA) with GAA.TTC repeat expansion in the Frataxin (FXN) gene's first intron (IGIBi016-A) and a non-FRDA healthy control individual (IGIBi017-A). Ahmad I; Kamai A; Zahra S; Kapoor H; Kumar Srivastava A; Faruq M Stem Cell Res; 2024 Jun; 77():103382. PubMed ID: 38484450 [TBL] [Abstract][Full Text] [Related]
5. The GAA repeat expansion in intron 1 of the frataxin gene is related to the severity of cardiac manifestation in patients with Friedreich's ataxia. Bit-Avragim N; Perrot A; Schöls L; Hardt C; Kreuz FR; Zühlke C; Bubel S; Laccone F; Vogel HP; Dietz R; Osterziel KJ J Mol Med (Berl); 2001; 78(11):626-32. PubMed ID: 11269509 [TBL] [Abstract][Full Text] [Related]
6. A multiple animal and cellular models approach to study frataxin deficiency in Friedreich Ataxia. Mosbach V; Puccio H Biochim Biophys Acta Mol Cell Res; 2024 Oct; 1871(7):119809. PubMed ID: 39134123 [TBL] [Abstract][Full Text] [Related]
7. Friedreich's ataxia--a case of aberrant transcription termination? Butler JS; Napierala M Transcription; 2015; 6(2):33-6. PubMed ID: 25831023 [TBL] [Abstract][Full Text] [Related]
8. DNA Base Damage Repair Crosstalks with Chromatin Structures to Contract Expanded GAA Repeats in Friedreich's Ataxia. Lai Y; Diaz N; Armbrister R; Agoulnik I; Liu Y Biomolecules; 2024 Jul; 14(7):. PubMed ID: 39062522 [TBL] [Abstract][Full Text] [Related]
9. Alleviating GAA Repeat Induced Transcriptional Silencing of the Friedreich's Ataxia Gene During Somatic Cell Reprogramming. Polak U; Li Y; Butler JS; Napierala M Stem Cells Dev; 2016 Dec; 25(23):1788-1800. PubMed ID: 27615158 [TBL] [Abstract][Full Text] [Related]
11. A Comprehensive Transcriptome Analysis Identifies FXN and BDNF as Novel Targets of miRNAs in Friedreich's Ataxia Patients. Misiorek JO; Schreiber AM; Urbanek-Trzeciak MO; Jazurek-Ciesiołka M; Hauser LA; Lynch DR; Napierala JS; Napierala M Mol Neurobiol; 2020 Jun; 57(6):2639-2653. PubMed ID: 32291635 [TBL] [Abstract][Full Text] [Related]
12. Identification of a novel missense mutation in Friedreich's ataxia -FXN Clark E; Strawser C; Schadt K; Lynch DR Ann Clin Transl Neurol; 2019 Apr; 6(4):812-816. PubMed ID: 31020006 [TBL] [Abstract][Full Text] [Related]
13. Stalled DNA Replication Forks at the Endogenous GAA Repeats Drive Repeat Expansion in Friedreich's Ataxia Cells. Gerhardt J; Bhalla AD; Butler JS; Puckett JW; Dervan PB; Rosenwaks Z; Napierala M Cell Rep; 2016 Aug; 16(5):1218-1227. PubMed ID: 27425605 [TBL] [Abstract][Full Text] [Related]
14. Friedreich's ataxia, frataxin, PIP5K1B: echo of a distant fracas. Bayot A; Rustin P Oxid Med Cell Longev; 2013; 2013():725635. PubMed ID: 24194977 [TBL] [Abstract][Full Text] [Related]
15. A Novel Metric for Predicting Severity of Disease Features in Friedreich's Ataxia. Rodden LN; Rummey C; Kessler S; Wilson RB; Lynch DR Mov Disord; 2023 Jun; 38(6):970-977. PubMed ID: 36928898 [TBL] [Abstract][Full Text] [Related]
16. Friedreich's ataxia and frataxin: molecular genetics, evolution and pathogenesis (Review). Palau F Int J Mol Med; 2001 Jun; 7(6):581-9. PubMed ID: 11351269 [TBL] [Abstract][Full Text] [Related]
17. Removal of the GAA repeat in the heart of a Friedreich's ataxia mouse model using CjCas9. Yaméogo P; Gérard C; Majeau N; Tremblay JP Gene Ther; 2023 Aug; 30(7-8):612-619. PubMed ID: 36781946 [TBL] [Abstract][Full Text] [Related]
18. Generation of transgene-free iPSC lines from three patients with Friedreich's ataxia (FRDA) carrying GAA triplet expansions in the first intron of FXN gene. Kelekçi S; Uğurlu-Çimen D; Demir AB; Özçimen B; Burak Yıldız A; Batuhan Karakuş M; Börklü Yücel E; Önder TT Stem Cell Res; 2021 Jul; 54():102438. PubMed ID: 34214898 [TBL] [Abstract][Full Text] [Related]
19. Complete FXN deletion in a patient with Friedreich's ataxia. van den Ouweland AM; van Minkelen R; Bolman GM; Wouters CH; Becht-Noordermeer C; Deelen WH; Deelen-Manders JM; Ippel EP; Saris J; Halley DJ Genet Test Mol Biomarkers; 2012 Sep; 16(9):1015-8. PubMed ID: 22691228 [TBL] [Abstract][Full Text] [Related]
20. GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology. Al-Mahdawi S; Pinto RM; Varshney D; Lawrence L; Lowrie MB; Hughes S; Webster Z; Blake J; Cooper JM; King R; Pook MA Genomics; 2006 Nov; 88(5):580-90. PubMed ID: 16919418 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]