Search Results - "Balendra, R."

Theme 05 - Human Cell Biology and Pathology.

Authors: Balendra, R. Ruiz de los Mozos, I. Odeh, H. et al.

Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 2023 Suppl1, Vol. 24, p140-160. 21p.

Theme 1 Epidemiology and informatics.

Authors: Armon, Carmel Pupillo, Elisabetta Bianchi, Elisa et al.

Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 2019 Supplement, Vol. 20, p101-113. 13p.

Theme 5 Human Cell Biology and Pathology.

Authors: Boivin, M.-N. Ferry, N. LaFleur, K. et al.

Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 2024 Suppl 1, Vol. 25, p158-184. 27p.

Theme 4 In Vivo Experimental Models.

Authors: Vandenakker, A. Bird, S. Curzio, D. D. et al.

Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 2024 Suppl 1, Vol. 25, p136-157. 22p.

Multi-regional transcriptomic profiling reveals divergent molecular mechanisms in ALS-related neurodegeneration.

Authors: Hsu, Yu-Wen Lu, Yu-Ning Liu, Mingming et al.

Source: PLoS Genetics. 7/8/2026, Vol. 22 Issue 7, p1-24. 24p.

Effects of Loop Nucleobase Substitution on G-Quadruplex Thermal Stability in Aqueous Glycine Betaine, Proline, TMAO, and Urea Solutions.

Authors: Schwinefus, Jeffrey J. Corluka, Marija Dobrinski, Isabella et al.

Source: Biomolecules (2218-273X). May2026, Vol. 16 Issue 5, p697. 17p.

Real-world prognostic role of riluzole use in ALS: a multi-center study from PRECISION-ALS.

Authors: Vasta, Rosario Ombelet, Fouke Hobin, Frederik et al.

Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 2025 Suppl 1, Vol. 26, p50-60. 11p.

Clinical trajectories of genetic variants in ALS: a European observational study within PRECISION-ALS.

Authors: McFarlane, Robert Opie-Martin, Sarah Caravaca Puchades, Alejandro et al.

Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 2025 Suppl 1, Vol. 26, p41-49. 9p.

Author Index.

Source: Amyotrophic Lateral Sclerosis. Oct2012 Supplement, Vol. 13, p189-194. 6p.

Genetic risk for neurodegenerative conditions is linked to disease-specific microglial pathways.

Authors: Askarova, Aydan Yaa, Reuben M. Marzi, Sarah J. et al.

Source: PLoS Genetics. 4/9/2025, Vol. 21 Issue 4, p1-23. 23p.

Loss of Pol III repressor Maf1 in neurons promotes longevity by preventing the age-related decline in 5S rRNA and translation.

Authors: Xu, Bowen Hull, Alexander Hill, Olivia N. M. et al.

Source: PLoS Biology. 7/15/2025, Vol. 23 Issue 7, p1-21. 21p.

TIA1 Mutant Mouse Model Exhibits Motor Deficits and Neurodegenerative Characteristics of Amyotrophic Lateral Sclerosis.

Authors: Mao, Li-Hong Song, Yu-Ning Zhang, Jing-Qi et al.

Source: Cells (2073-4409). Mar2026, Vol. 15 Issue 5, p420. 20p.

Selective Silencing of TDP-43 P. G376D Mutation Reverses Key Amyotrophic Lateral Sclerosis-Related Cellular Deficits.

Authors: Romano, Roberta Ruotolo, Giorgia Perrone, Francesco et al.

Source: Biomolecules (2218-273X). Mar2026, Vol. 16 Issue 3, p393. 17p.

Analysis of normal C9orf72 repeat length as possible disease modifier in amyotrophic lateral sclerosis.

Authors: Peverelli, Silvia Brusati, Alberto Casiraghi, Valeria et al.

Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Feb2024, Vol. 25 Issue 1/2, p207-210. 4p.

Amyotrophic lateral sclerosis caused by TARDBP mutations: from genetics to TDP-43 proteinopathy.

Authors: Balendra R Sreedharan J Hallegger M et al.

Source: The Lancet. Neurology [Lancet Neurol] 2025 May; Vol. 24 (5), pp. 456-470.

Publication Type: Journal Article; Review

Journal Info: Publisher: Lancet Pub. Group Country of Publication: England NLM ID: 101139309 Publication Model: Print Cited Medium: Internet ISSN: 1474-4465 (Electronic) Linking ISSN: 14744422 NLM ISO Abbreviation: Lancet Neurol Subsets: MEDLINE

Microglial Dysfunction Induced by C9ORF72 Dipeptide Repeat Proteins: Biomarker and Therapeutic Perspectives.

Authors: Sharma, Niti An, Seong Soo A.

Source: International Journal of Molecular Sciences. Jun2026, Vol. 27 Issue 12, p5537. 16p.

Epigenetic Evidence Implies Disturbed Proteostasis and Potentially Protein Aggregation in Suicidality.

Authors: Šmon, Julija Juković, Maja Kršanac, Matea et al.

Source: Biomolecules (2218-273X). May2026, Vol. 16 Issue 5, p733. 30p.

G4 Oligonucleotide-Based Chaperones of Heterogeneous Nuclear Ribonucleoprotein A1.

Authors: Malakhova, Elizaveta Svetlova, Julia Pavlova, Iuliia et al.

Source: International Journal of Molecular Sciences. Oct2025, Vol. 26 Issue 20, p10104. 18p.

Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease.

Authors: Bhattacharyya, Nihar Chai, Niuzheng Hafford-Tear, Nathaniel J. et al.

Source: PLoS Genetics. 5/7/2024, Vol. 20 Issue 5, p1-27. 27p.

Wear Reduction on the Roller–Shoe Mechanism at High Operation Loads.

Authors: Iordache, Constantin Răzvan Bujoreanu, Carmen Alaci, Stelian et al.

Source: Coatings (2079-6412); Mar2024, Vol. 14 Issue 3, p316, 19p