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 *

121 related articles for article (PubMed ID: 18270236)

  • 21. PFN1 mutations are rare in Han Chinese populations with amyotrophic lateral sclerosis.
    Chen Y; Zheng ZZ; Huang R; Chen K; Song W; Zhao B; Chen X; Yang Y; Yuan L; Shang HF
    Neurobiol Aging; 2013 Jul; 34(7):1922.e1-5. PubMed ID: 23428184
    [TBL] [Abstract][Full Text] [Related]  

  • 22. TARDBP gene mutations among Chinese patients with sporadic amyotrophic lateral sclerosis.
    Huang R; Fang DF; Ma MY; Guo XY; Zhao B; Zeng Y; Zhou D; Yang Y; Shang HF
    Neurobiol Aging; 2012 May; 33(5):1015.e1-6. PubMed ID: 20708823
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population.
    Chen X; Huang R; Chen Y; Zheng Z; Chen K; Song W; Zhao B; Yang Y; Yuan L; Shang H
    Neurol Sci; 2014 Jul; 35(7):1089-95. PubMed ID: 24493373
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Screening the metallothionein III gene in sporadic amyotrophic lateral sclerosis.
    Morahan JM; Yu B; Trent RJ; Pamphlett R
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Jun; 6(2):115-7. PubMed ID: 16036436
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mutation analysis of VCP in familial and sporadic amyotrophic lateral sclerosis.
    Williams KL; Solski JA; Nicholson GA; Blair IP
    Neurobiol Aging; 2012 Jul; 33(7):1488.e15-6. PubMed ID: 22196955
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Alteration of the Neuromuscular Junction and Modifications of Muscle Metabolism in Response to Neuron-Restricted Expression of the CHMP2B
    Waegaert R; Dirrig-Grosch S; Liu H; Boutry M; Luan P; Loeffler JP; René F
    Biomolecules; 2022 Mar; 12(4):. PubMed ID: 35454086
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [The association between angiogenin gene variations and familial amyotrophic lateral sclerosis in Chinese Han patients].
    Zhang H; Zhang Y; Tang L; Zhang N; Fan D
    Zhonghua Nei Ke Za Zhi; 2015 Feb; 54(2):122-4. PubMed ID: 25907842
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis.
    Nakamura R; Misawa K; Tohnai G; Nakatochi M; Furuhashi S; Atsuta N; Hayashi N; Yokoi D; Watanabe H; Watanabe H; Katsuno M; Izumi Y; Kanai K; Hattori N; Morita M; Taniguchi A; Kano O; Oda M; Shibuya K; Kuwabara S; Suzuki N; Aoki M; Ohta Y; Yamashita T; Abe K; Hashimoto R; Aiba I; Okamoto K; Mizoguchi K; Hasegawa K; Okada Y; Ishihara T; Onodera O; Nakashima K; Kaji R; Kamatani Y; Ikegawa S; Momozawa Y; Kubo M; Ishida N; Minegishi N; Nagasaki M; Sobue G
    Commun Biol; 2020 Sep; 3(1):526. PubMed ID: 32968195
    [TBL] [Abstract][Full Text] [Related]  

  • 29. CHMP2B mutations are not a common cause of frontotemporal lobar degeneration.
    Cannon A; Baker M; Boeve B; Josephs K; Knopman D; Petersen R; Parisi J; Dickison D; Adamson J; Snowden J; Neary D; Mann D; Hutton M; Pickering-Brown SM
    Neurosci Lett; 2006 May; 398(1-2):83-4. PubMed ID: 16431024
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutations in the profilin 1 gene are not common in amyotrophic lateral sclerosis of Chinese origin.
    Zou ZY; Sun Q; Liu MS; Li XG; Cui LY
    Neurobiol Aging; 2013 Jun; 34(6):1713.e5-6. PubMed ID: 23357624
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Screening of the TBK1 gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.
    Shu S; Li XL; Liu Q; Liu F; Cui B; Liu MS; Cui LY; Li XG; Zhang X
    Amyotroph Lateral Scler Frontotemporal Degener; 2016; 17(7-8):605-607. PubMed ID: 27260353
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Association between the Angiogenin (ANG) K17I variant and amyotrophic lateral sclerosis risk in Caucasian: a meta-analysis.
    Pan L; Deng X; Ding D; Leng H; Zhu X; Wang Z
    Neurol Sci; 2015 Dec; 36(12):2163-8. PubMed ID: 26255299
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis.
    Zou ZY; Zhou ZR; Che CH; Liu CY; He RL; Huang HP
    J Neurol Neurosurg Psychiatry; 2017 Jul; 88(7):540-549. PubMed ID: 28057713
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis.
    Belzil VV; Daoud H; Desjarlais A; Bouchard JP; Dupré N; Camu W; Dion PA; Rouleau GA
    Neurobiol Aging; 2011 Mar; 32(3):555.e13-4. PubMed ID: 21074290
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel FUS/TLS mutations and pathology in familial and sporadic amyotrophic lateral sclerosis.
    Hewitt C; Kirby J; Highley JR; Hartley JA; Hibberd R; Hollinger HC; Williams TL; Ince PG; McDermott CJ; Shaw PJ
    Arch Neurol; 2010 Apr; 67(4):455-61. PubMed ID: 20385912
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Screening for OPTN mutations in amyotrophic lateral sclerosis in a mainly Caucasian population.
    Sugihara K; Maruyama H; Kamada M; Morino H; Kawakami H
    Neurobiol Aging; 2011 Oct; 32(10):1923.e9-10. PubMed ID: 21550138
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis.
    Fifita JA; Zhang KY; Galper J; Williams KL; McCann EP; Hogan AL; Saunders N; Bauer D; Tarr IS; Pamphlett R; Nicholson GA; Rowe D; Yang S; Blair IP
    Neurodegener Dis; 2017; 17(6):304-312. PubMed ID: 29131108
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Screening for C9orf72 repeat expansions in Chinese amyotrophic lateral sclerosis patients.
    Zou ZY; Li XG; Liu MS; Cui LY
    Neurobiol Aging; 2013 Jun; 34(6):1710.e5-6. PubMed ID: 23261768
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetics of sporadic amyotrophic lateral sclerosis.
    Schymick JC; Talbot K; Traynor BJ
    Hum Mol Genet; 2007 Oct; 16 Spec No. 2():R233-42. PubMed ID: 17911166
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis.
    Belzil VV; André-Guimont C; Atallah MR; Daoud H; Dupré N; Bouchard JP; Camu W; Dion PA; Rouleau GA
    Neurobiol Aging; 2012 Aug; 33(8):1845.e7-9. PubMed ID: 22361451
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.