BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 35315050)

  • 1. [Advance in research on pathogenetic genes for amyotrophic lateral sclerosis].
    Zhao H; Niu Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Mar; 39(3):343-349. PubMed ID: 35315050
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The prognostic value of systematic genetic screening in amyotrophic lateral sclerosis patients.
    He D; Liu Y; Dong S; Shen D; Yang X; Hao M; Yin X; He X; Li Y; Wang Y; Liu M; Wang J; Chen X; Cui L
    J Neurol; 2024 Mar; 271(3):1385-1396. PubMed ID: 37980296
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Knowledge-Based Machine Learning Approach to Gene Prioritisation in Amyotrophic Lateral Sclerosis.
    Bean DM; Al-Chalabi A; Dobson RJB; Iacoangeli A
    Genes (Basel); 2020 Jun; 11(6):. PubMed ID: 32575372
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic overlap between ALS and other neurodegenerative or neuromuscular disorders.
    Olsen CG; Busk ØL; Holla ØL; Tveten K; Holmøy T; Tysnes OB; Høyer H
    Amyotroph Lateral Scler Frontotemporal Degener; 2024 Feb; 25(1-2):177-187. PubMed ID: 37849306
    [TBL] [Abstract][Full Text] [Related]  

  • 5. MicroRNAs in amyotrophic lateral sclerosis: from pathogenetic involvement to diagnostic biomarker and therapeutic agent development.
    Wang L; Zhang L
    Neurol Sci; 2020 Dec; 41(12):3569-3577. PubMed ID: 33006054
    [TBL] [Abstract][Full Text] [Related]  

  • 6. OPTN p.Met468Arg and ATXN2 intermediate length polyQ extension in families with C9orf72 mediated amyotrophic lateral sclerosis and frontotemporal dementia.
    Farhan SMK; Gendron TF; Petrucelli L; Hegele RA; Strong MJ
    Am J Med Genet B Neuropsychiatr Genet; 2018 Jan; 177(1):75-85. PubMed ID: 29080331
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Advance in research on biomarkers for amyotrophic lateral sclerosis].
    Cheng Y; Chen Y; Shang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Apr; 38(4):383-387. PubMed ID: 33834472
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Update on amyotrophic lateral sclerosis genetics.
    Brenner D; Weishaupt JH
    Curr Opin Neurol; 2019 Oct; 32(5):735-739. PubMed ID: 31335339
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Amyotrophic Lateral Sclerosis Genes in
    Layalle S; They L; Ourghani S; Raoul C; Soustelle L
    Int J Mol Sci; 2021 Jan; 22(2):. PubMed ID: 33477509
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Emerging understanding of the genotype-phenotype relationship in amyotrophic lateral sclerosis.
    Goutman SA; Chen KS; Paez-Colasante X; Feldman EL
    Handb Clin Neurol; 2018; 148():603-623. PubMed ID: 29478603
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Heterozygous
    Osmanovic A; Gogol I; Martens H; Widjaja M; Müller K; Schreiber-Katz O; Feuerhake F; Langhans CD; Schmidt G; Andersen PM; Ludolph AC; Weishaupt JH; Brand F; Petri S; Weber RG
    Genes (Basel); 2021 Dec; 13(1):. PubMed ID: 35052424
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of GGC repeat expansion in the
    Yuan Y; Liu Z; Hou X; Li W; Ni J; Huang L; Hu Y; Liu P; Hou X; Xue J; Sun Q; Tian Y; Jiao B; Duan R; Jiang H; Shen L; Tang B; Wang J
    Neurology; 2020 Dec; 95(24):e3394-e3405. PubMed ID: 32989102
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical neurogenetics: amyotrophic lateral sclerosis.
    Harms MB; Baloh RH
    Neurol Clin; 2013 Nov; 31(4):929-50. PubMed ID: 24176417
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genotype-property patient-phenotype relations suggest that proteome exhaustion can cause amyotrophic lateral sclerosis.
    Kepp KP
    PLoS One; 2015; 10(3):e0118649. PubMed ID: 25798606
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pathogenic Genome Signatures That Damage Motor Neurons in Amyotrophic Lateral Sclerosis.
    Yousefian-Jazi A; Seol Y; Kim J; Ryu HL; Lee J; Ryu H
    Cells; 2020 Dec; 9(12):. PubMed ID: 33333804
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular basis of amyotrophic lateral sclerosis.
    Liscic RM; Breljak D
    Prog Neuropsychopharmacol Biol Psychiatry; 2011 Mar; 35(2):370-2. PubMed ID: 20655970
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Common mutations of interest in the diagnosis of amyotrophic lateral sclerosis: how common are common mutations in ALS genes?
    Perrone B; Conforti FL
    Expert Rev Mol Diagn; 2020 Jul; 20(7):703-714. PubMed ID: 32497448
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis.
    Piaceri I; Del Mastio M; Tedde A; Bagnoli S; Latorraca S; Massaro F; Paganini M; Corrado A; Sorbi S; Nacmias B
    Clin Genet; 2012 Jul; 82(1):83-7. PubMed ID: 21651514
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis.
    Stoccoro A; Smith AR; Mosca L; Marocchi A; Gerardi F; Lunetta C; Cereda C; Gagliardi S; Lunnon K; Migliore L; Coppedè F
    Clin Epigenetics; 2020 Sep; 12(1):137. PubMed ID: 32917270
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Metal(loid)s role in the pathogenesis of amyotrophic lateral sclerosis: Environmental, epidemiological, and genetic data.
    Tesauro M; Bruschi M; Filippini T; D'Alfonso S; Mazzini L; Corrado L; Consonni M; Vinceti M; Fusi P; Urani C
    Environ Res; 2021 Jan; 192():110292. PubMed ID: 33027627
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.