| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Daniela Scarabino, Liana Veneziano, Suran Nethisinghe, Elide Mantuano, Alessia Fiore, Giulia Granata, Nita Solanky, Ginevra Zanni, Francesca Cavalcanti, Rosa Maria Corbo, Paola Giunt. Unusual Age-Dependent Behavior of Leukocytes Telomere Length in Friedreich's Ataxia. Movement disorders : official journal of the Movement Disorder Society. 2024-09-05. PMID:39235665. |
friedreich ataxia (frda) is an autosomal recessive neurodegenerative disorder caused by an expanded gaa repeat in the first intron of the fxn gene. |
2024-09-05 |
2024-09-08 |
Not clear |
| Lin Wu, Fei Huang, Lu Yang, Liu Yang, Zichen Sun, Jinghua Zhang, Siyu Xia, Hongting Zhao, Yibing Ding, Dezhi Bian, Kuanyu L. Interplay of FXN expression and lipolysis in white adipocytes plays a critical role in insulin sensitivity in Friedreich's ataxia mouse model. Scientific reports. vol 14. issue 1. 2024-08-27. PMID:39191875. |
frataxin (fxn) is required for iron-sulfur cluster biogenesis, and its loss causes the early-onset neurodegenerative disease friedreich ataxia (frda). |
2024-08-27 |
2024-08-30 |
mouse |
| Andrés Vicente-Acosta, Saúl Herranz-Martín, María Ruth Pazos, Jorge Galán-Cruz, Mario Amores, Frida Loria, Javier Díaz-Nid. Glial cell activation precedes neurodegeneration in the cerebellar cortex of the YG8-800 murine model of Friedreich ataxia. Neurobiology of disease. 2024-08-07. PMID:39111701. |
friedreich ataxia is a hereditary neurodegenerative disorder resulting from reduced levels of the protein frataxin due to an expanded gaa repeat in the fxn gene. |
2024-08-07 |
2024-08-10 |
mouse |
| Andrés Vicente-Acosta, Saúl Herranz-Martín, María Ruth Pazos, Jorge Galán-Cruz, Mario Amores, Frida Loria, Javier Díaz-Nid. Glial cell activation precedes neurodegeneration in the cerebellar cortex of the YG8-800 murine model of Friedreich ataxia. Neurobiology of disease. 2024-08-07. PMID:39111701. |
in this work, we followed and characterized the progression of changes in the cerebellar cortex in the latest version of friedreich ataxia humanized mouse model, yg8-800 (fxn |
2024-08-07 |
2024-08-10 |
mouse |
| Estelle Jullian, Maria Russi, Ema Turki, Margaux Bouvelot, Laura Tixier, Sandrine Middendorp, Elodie Martin, Véronique Monnie. Glial overexpression of Tspo extends lifespan and protects against frataxin deficiency in Drosophila. Biochimie. 2024-05-16. PMID:38750879. |
friedreich ataxia (fa) is a neurodegenerative disease due to gaa expansions in the fxn gene leading to decreased expression of frataxin, a mitochondrial protein involved in the biosynthesis of iron-sulfur clusters. |
2024-05-16 |
2024-05-27 |
human |
| Christian Rummey, Susan Perlman, Sub H Subramony, Jennifer Farmer, David R Lync. Evaluating mFARS in pediatric Friedreich's ataxia: Insights from the FACHILD study. Annals of clinical and translational neurology. 2024-04-01. PMID:38556905. |
friedreich ataxia (frda) is a rare genetic disorder caused by mutations in the fxn gene, leading to progressive coordination loss and other symptoms. |
2024-04-01 |
2024-04-03 |
Not clear |
| Megan M Shen, Christian Rummey, David R Lync. Phenotypic variation of FXN compound heterozygotes in a Friedreich ataxia cohort. Annals of clinical and translational neurology. 2024-02-24. PMID:38396238. |
phenotypic variation of fxn compound heterozygotes in a friedreich ataxia cohort. |
2024-02-24 |
2024-02-26 |
Not clear |
| Megan M Shen, Christian Rummey, David R Lync. Phenotypic variation of FXN compound heterozygotes in a Friedreich ataxia cohort. Annals of clinical and translational neurology. 2024-02-24. PMID:38396238. |
most individuals with friedreich ataxia (frda) have homozygous gaa triplet repeat expansions in the fxn gene, correlating with a typical phenotype of ataxia and cardiomyopathy. |
2024-02-24 |
2024-02-26 |
Not clear |
| Doni Davide, Cavion Federica, Bortolus Marco, Baschiera Elisa, Muccioli Silvia, Tombesi Giulia, d'Ettorre Federica, Daniele Ottaviani, Marchesan Elena, Leanza Luigi, Greggio Elisa, Ziviani Elena, Russo Antonella, Bellin Milena, Sartori Geppo, Carbonera Donatella, Salviati Leonardo, Costantini Paol. Human frataxin, the Friedreich ataxia deficient protein, interacts with mitochondrial respiratory chain. Cell death & disease. vol 14. issue 12. 2023-12-07. PMID:38062036. |
friedreich ataxia (frda) is a rare, inherited neurodegenerative disease caused by an expanded gaa repeat in the first intron of the fxn gene, leading to transcriptional silencing and reduced expression of frataxin. |
2023-12-07 |
2023-12-17 |
human |
| Cinthia Aguilera, Anna Esteve-Garcia, Carlos Casasnovas, Valentina Vélez-Santamaria, Laura Rausell, Pablo Gargallo, Javier Garcia-Planells, Pedro Alía, Núria Llecha, Ariadna Padró-Mique. Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: may be more prevalent than we think? BMC medical genomics. vol 16. issue 1. 2023-12-02. PMID:38041144. |
novel intragenic deletion within the fxn gene in a patient with typical phenotype of friedreich ataxia: may be more prevalent than we think? |
2023-12-02 |
2023-12-10 |
Not clear |
| Cinthia Aguilera, Anna Esteve-Garcia, Carlos Casasnovas, Valentina Vélez-Santamaria, Laura Rausell, Pablo Gargallo, Javier Garcia-Planells, Pedro Alía, Núria Llecha, Ariadna Padró-Mique. Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: may be more prevalent than we think? BMC medical genomics. vol 16. issue 1. 2023-12-02. PMID:38041144. |
friedreich ataxia is the most common inherited ataxia in europe and is mainly caused by biallelic pathogenic expansions of the gaa trinucleotide repeat in intron 1 of the fxn gene that lead to a decrease in frataxin protein levels. |
2023-12-02 |
2023-12-10 |
Not clear |
| Saumya Maheshwari, Gabriela Vilema-Enríquez, Richard Wade-Martin. Patient-derived iPSC models of Friedreich ataxia: a new frontier for understanding disease mechanisms and therapeutic application. Translational neurodegeneration. vol 12. issue 1. 2023-09-19. PMID:37726850. |
friedreich ataxia (frda) is a rare genetic multisystem disorder caused by a pathological gaa trinucleotide repeat expansion in the fxn gene. |
2023-09-19 |
2023-10-07 |
Not clear |
| Maria M Krasilnikova, Casey L Humphries, Emily M Shinsk. Friedreich's ataxia: new insights. Emerging topics in life sciences. 2023-09-12. PMID:37698160. |
friedreich ataxia (frda) is an inherited disease that is typically caused by gaa repeat expansion within the first intron of the fxn gene coding for frataxin. |
2023-09-12 |
2023-10-07 |
Not clear |
| Camille Bouchard, Catherine Gérard, Solange Gni-Fiene Yanyabé, Nathalie Majeau, Malek Aloui, Gabrielle Buisson, Pouiré Yameogo, Vanessa Couture, Jacques P Trembla. Finding an Appropriate Mouse Model to Study the Impact of a Treatment for Friedreich Ataxia on the Behavioral Phenotype. Genes. vol 14. issue 8. 2023-08-26. PMID:37628705. |
friedreich ataxia (frda) is a progressive neurodegenerative disease caused by a gaa repeat in the intron 1 of the frataxin gene (fxn) leading to a lower expression of the frataxin protein. |
2023-08-26 |
2023-09-07 |
mouse |
| Layne N Rodden, Kellie McIntyre, Medina Keita, Mckenzie Wells, Courtney Park, Victoria Profeta, Amy Waldman, Christian Rummey, Laura J Balcer, David R Lync. Retinal hypoplasia and degeneration result in vision loss in Friedreich ataxia. Annals of clinical and translational neurology. 2023-06-19. PMID:37334854. |
friedreich ataxia (frda) is an inherited condition caused by a gaa triplet repeat (gaa-tr) expansion in the fxn gene. |
2023-06-19 |
2023-08-14 |
Not clear |
| L Ramo. Dimorphic frataxin and its gene regulation by sex steroids in hamsters. Molecular genetics and genomics : MGG. 2023-03-17. PMID:36929169. |
the role of frataxin (fxn) has been studied extensively in friedreich ataxia patients, however, the molecular bases underlining the sex steroid-dependent gene expression profiles of fxn in adult tissues are unknown. |
2023-03-17 |
2023-08-14 |
Not clear |
| Pouiré Yaméogo, Catherine Gérard, Nathalie Majeau, Jacques P Trembla. Removal of the GAA repeat in the heart of a Friedreich's ataxia mouse model using CjCas9. Gene therapy. 2023-02-13. PMID:36781946. |
most friedreich ataxia (frda) cases are caused by the elongation of the gaa repeat (gaar) sequence in the first intron of the fxn gene, leading to a decrease of the frataxin protein expression. |
2023-02-13 |
2023-08-14 |
mouse |
| Catherine Gérard, Annabelle Fortin Archambault, Camille Bouchard, Jacques P Trembla. A promissing mouse model for Friedreich Ataxia progressing like human patients. Behavioural brain research. 2022-09-11. PMID:36089099. |
friedreich ataxia (frda) is a genetic disease caused by an expended gaa repeat in the fxn gene leading to a reduction in frataxin protein production. |
2022-09-11 |
2023-08-14 |
mouse |
| Thomas M O'Connell, David L Logsdon, R Mark Payn. Metabolomics analysis reveals dysregulation in one carbon metabolism in Friedreich Ataxia. Molecular genetics and metabolism. 2022-07-07. PMID:35798654. |
friedreich ataxia (fa) is a rare and often fatal autosomal recessive disease in which a mitochondrial protein, frataxin (fxn), is severely reduced in all tissues. |
2022-07-07 |
2023-08-14 |
human |
| Layne N Rodden, Kaitlyn M Gilliam, Christina Lam, Teerapat Rojsajjakul, Clementina Mesaros, Chiara Dionisi, Mark Pook, Massimo Pandolfo, David R Lynch, Ian A Blair, Sanjay I Bidichandan. DNA methylation in Friedreich ataxia silences expression of frataxin isoform E. Scientific reports. vol 12. issue 1. 2022-03-24. PMID:35322126. |
dna methylation in friedreich ataxia silences expression of frataxin isoform e. epigenetic silencing in friedreich ataxia (frda), induced by an expanded gaa triplet-repeat in intron 1 of the fxn gene, results in deficiency of the mitochondrial protein, frataxin. |
2022-03-24 |
2023-08-13 |
mouse |