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Academic Journal

No Association of Multiple Sclerosis with C9orf72 Hexanucleotide Repeat Size in an Austrian Cohort.

Authors : König, Theresa^1,2 (AUTHOR) ; Leutmezer, Fritz^1,2 (AUTHOR) ; Berger, Thomas^1,2 (AUTHOR)

Source: International Journal of Molecular Sciences. Jul2023, Vol. 24 Issue 14, p11254. 9p.

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G-Quadruplexes Formation by the C9orf72 Nucleotide Repeat Expansion d(GGGGCC) n and Conformation Regulation by Fangchinoline.

Authors : Zhang, Yun¹ (AUTHOR); Huang, Junliu¹ (AUTHOR); Yu, Kainan¹ (AUTHOR)

Source: Molecules. Jun2023, Vol. 28 Issue 12, p4671. 14p.

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Academic Journal

Roadmap for C9ORF72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis: Report on the C9ORF72 FTD/ALS Summit.

Authors : Sattler, Rita¹ (AUTHOR) ; Traynor, Bryan J.² (AUTHOR); Robertson, Janice³ (AUTHOR)

Source: Neurology & Therapy. Dec2023, Vol. 12 Issue 6, p1821-1843. 23p.

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A toxic gain-of-function mechanism in C9orf72 ALS impairs the autophagy-lysosome pathway in neurons.

Authors : Beckers, Jimmy^1,2 (AUTHOR) ; Tharkeshwar, Arun Kumar^1,2,3 (AUTHOR); Fumagalli, Laura^4,5 (AUTHOR)

Source: Acta Neuropathologica Communications. 9/18/2023, Vol. 11 Issue 1, p1-22. 22p.

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Insight into Tetramolecular DNA G-Quadruplexes Associated with ALS and FTLD: Cation Interactions and Formation of Higher-Ordered Structure.

Authors : Zalar, Matja¹ (AUTHOR) ; Wang, Baifan¹ (AUTHOR) ; Plavec, Janez^1,2,3 (AUTHOR)

Source: International Journal of Molecular Sciences. Sep2023, Vol. 24 Issue 17, p13437. 19p.

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Medium-Chain Fatty Acids Rescue Motor Function and Neuromuscular Junction Degeneration in a Drosophila Model of Amyotrophic Lateral Sclerosis.

Authors : Dunn, Ella¹ (AUTHOR) ; Steinert, Joern R.² (AUTHOR) ; Stone, Aelfwin² (AUTHOR)

Source: Cells (2073-4409). Sep2023, Vol. 12 Issue 17, p2163. 19p.

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Academic Journal

Repeat length of C9orf72-associated glycine–alanine polypeptides affects their toxicity.

Authors : Morón-Oset, Javier¹ (AUTHOR); Fischer, Lilly Katharina Sophie¹ (AUTHOR); Jauré, Nathalie¹ (AUTHOR)

Source: Acta Neuropathologica Communications. 8/29/2023, Vol. 11 Issue 1, p1-28. 28p.

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Clinical testing panels for ALS: global distribution, consistency, and challenges.

Authors : Dilliott, Allison A.¹ (AUTHOR); Al Nasser, Ahmad² (AUTHOR); Elnagheeb, Marwa³ (AUTHOR)

Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Aug2023, Vol. 24 Issue 5/6, p420-435. 16p.

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Academic Journal

Frequency of C9orf72 and SOD1 mutations in 302 sporadic ALS patients from three German ALS centers.

Authors : Yilmaz, Rüstem¹ (AUTHOR); Grehl, Torsten² (AUTHOR); Eckrich, Lukas¹ (AUTHOR)

Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Aug2023, Vol. 24 Issue 5/6, p414-419. 6p.

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Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain.

Authors : Baviera‐Muñoz, Raquel^1,2,3,4 (AUTHOR); Carretero‐Vilarroig, Lidón^2,3,5 (AUTHOR); Muelas, Nuria^1,2,3,6,7 (AUTHOR)

Source: Movement Disorders Clinical Practice. Jun2023, Vol. 10 Issue 6, p992-997. 6p.

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فلترة النتائج

No Association of Multiple Sclerosis with C9orf72 Hexanucleotide Repeat Size in an Austrian Cohort.

G-Quadruplexes Formation by the C9orf72 Nucleotide Repeat Expansion d(GGGGCC) n and Conformation Regulation by Fangchinoline.

Roadmap for C9ORF72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis: Report on the C9ORF72 FTD/ALS Summit.

A toxic gain-of-function mechanism in C9orf72 ALS impairs the autophagy-lysosome pathway in neurons.

Insight into Tetramolecular DNA G-Quadruplexes Associated with ALS and FTLD: Cation Interactions and Formation of Higher-Ordered Structure.

Medium-Chain Fatty Acids Rescue Motor Function and Neuromuscular Junction Degeneration in a Drosophila Model of Amyotrophic Lateral Sclerosis.

Repeat length of C9orf72-associated glycine–alanine polypeptides affects their toxicity.

Clinical testing panels for ALS: global distribution, consistency, and challenges.

Frequency of C9orf72 and SOD1 mutations in 302 sporadic ALS patients from three German ALS centers.

Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain.

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