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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

195 related articles for article (PubMed ID: 29102476)

  • 21. The genotype-phenotype landscape of familial amyotrophic lateral sclerosis in Australia.
    McCann EP; Williams KL; Fifita JA; Tarr IS; O'Connor J; Rowe DB; Nicholson GA; Blair IP
    Clin Genet; 2017 Sep; 92(3):259-266. PubMed ID: 28105640
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Accuracy of a machine learning method based on structural and locational information from AlphaFold2 for predicting the pathogenicity of TARDBP and FUS gene variants in ALS.
    Hatano Y; Ishihara T; Onodera O
    BMC Bioinformatics; 2023 May; 24(1):206. PubMed ID: 37208601
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cyclin F, Neurodegeneration, and the Pathogenesis of ALS/FTD.
    Rayner SL; Hogan A; Davidson JM; Cheng F; Luu L; Morsch M; Blair I; Chung R; Lee A
    Neuroscientist; 2024 Apr; 30(2):214-228. PubMed ID: 36062310
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutation analysis and immunopathological studies of PFN1 in familial and sporadic amyotrophic lateral sclerosis.
    Yang S; Fifita JA; Williams KL; Warraich ST; Pamphlett R; Nicholson GA; Blair IP
    Neurobiol Aging; 2013 Sep; 34(9):2235.e7-10. PubMed ID: 23635659
    [TBL] [Abstract][Full Text] [Related]  

  • 25. TDP-43 is a ubiquitylation substrate of the SCF
    Rayner SL; Yang S; Farrawell NE; Jagaraj CJ; Cheng F; Davidson JM; Luu L; Redondo AG; Rábano A; Borrego-Hernández D; Atkin JD; Morsch M; Blair IP; Yerbury JJ; Chung R; Lee A
    Neurobiol Dis; 2022 Jun; 167():105673. PubMed ID: 35231559
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of a novel missense mutation in angiogenin in a Chinese amyotrophic lateral sclerosis cohort.
    Zou ZY; Wang XN; Liu MS; Sun Q; Li XG; Cui LY; Kong J
    Amyotroph Lateral Scler; 2012 May; 13(3):270-5. PubMed ID: 22292798
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Zebrafish CCNF and FUS Mediate Stress-Specific Motor Responses.
    Aksoy YA; Cole AJ; Deng W; Hesselson D
    Cells; 2024 Feb; 13(5):. PubMed ID: 38474336
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Targeted next-generation sequencing reveals novel and rare variants in Indian patients with amyotrophic lateral sclerosis.
    Narain P; Pandey A; Gupta S; Gomes J; Bhatia R; Vivekanandan P
    Neurobiol Aging; 2018 Nov; 71():265.e9-265.e14. PubMed ID: 29895397
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China.
    Hou L; Jiao B; Xiao T; Zhou L; Zhou Z; Du J; Yan X; Wang J; Tang B; Shen L
    Sci Rep; 2016 Sep; 6():32478. PubMed ID: 27604643
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification of novel
    Wang F; Fu S; Lei J; Wu H; Shi S; Chen K; Hu J; Xu X
    Aging (Albany NY); 2020 Nov; 12(22):22859-22868. PubMed ID: 33159016
    [TBL] [Abstract][Full Text] [Related]  

  • 31. CHCHD10 mutations in patients with amyotrophic lateral sclerosis in Mainland China.
    Shen S; He J; Tang L; Zhang N; Fan D
    Neurobiol Aging; 2017 Jun; 54():214.e7-214.e10. PubMed ID: 28318595
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutation analysis of the TIA1 gene in Chinese patients with amyotrophic lateral sclerosis and frontotemporal dementia.
    Yuan Z; Jiao B; Hou L; Xiao T; Liu X; Wang J; Xu J; Zhou L; Yan X; Tang B; Shen L
    Neurobiol Aging; 2018 Apr; 64():160.e9-160.e12. PubMed ID: 29370934
    [TBL] [Abstract][Full Text] [Related]  

  • 33. CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients.
    Chiò A; Mora G; Sabatelli M; Caponnetto C; Traynor BJ; Johnson JO; Nalls MA; Calvo A; Moglia C; Borghero G; Monsurrò MR; La Bella V; Volanti P; Simone I; Salvi F; Logullo FO; Nilo R; Battistini S; Mandrioli J; Tanel R; Murru MR; Mandich P; Zollino M; Conforti FL; ; Brunetti M; Barberis M; Restagno G; Penco S; Lunetta C
    Neurobiol Aging; 2015 Apr; 36(4):1767.e3-1767.e6. PubMed ID: 25726362
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Four novel optineurin mutations in patients with sporadic amyotrophic lateral sclerosis in Mainland China.
    Yang L; Cheng Y; Jia X; Liu X; Li X; Zhang K; Shen D; Liu M; Guan Y; Liu Q; Cui L; Li X
    Neurobiol Aging; 2021 Jan; 97():149.e1-149.e8. PubMed ID: 32893042
    [TBL] [Abstract][Full Text] [Related]  

  • 35. ALS-linked loss of Cyclin-F function affects HSP90.
    Siebert A; Gattringer V; Weishaupt JH; Behrends C
    Life Sci Alliance; 2022 Sep; 5(12):. PubMed ID: 36114006
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Absence of mutations in exon 6 of the TARDBP gene in 207 Chinese patients with sporadic amyotrohic lateral sclerosis.
    Ye CH; Lu XL; Zheng MY; Zhen J; Li ZP; Shi L; Liu ZY; Feng LY; Pei Z; Yao XL
    PLoS One; 2013; 8(7):e68106. PubMed ID: 23874513
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementia.
    Yang X; Sun X; Liu Q; Liu L; Li J; Cai Z; Zhang K; Liu S; He D; Shen D; Liu M; Cui L; Zhang X
    Orphanet J Rare Dis; 2022 Nov; 17(1):404. PubMed ID: 36345033
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts.
    Ingre C; Landers JE; Rizik N; Volk AE; Akimoto C; Birve A; Hübers A; Keagle PJ; Piotrowska K; Press R; Andersen PM; Ludolph AC; Weishaupt JH
    Neurobiol Aging; 2013 Jun; 34(6):1708.e1-6. PubMed ID: 23141414
    [TBL] [Abstract][Full Text] [Related]  

  • 39. DCTN1 gene analysis in Chinese patients with sporadic amyotrophic lateral sclerosis.
    Liu X; Yang L; Tang L; Chen L; Liu X; Fan D
    PLoS One; 2017; 12(8):e0182572. PubMed ID: 28792508
    [TBL] [Abstract][Full Text] [Related]  

  • 40. High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis.
    Xu GR; Hu W; Zhan LL; Wang C; Xu LQ; Lin MT; Chen WJ; Wang N; Zhang QJ
    BMC Neurol; 2018 Apr; 18(1):35. PubMed ID: 29621978
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.