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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2001 | 2 |
2008 | 1 |
2024 | 0 |
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3 results
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Page 1
Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease.
Nat Genet. 2001 Jan;27(1):117-20. doi: 10.1038/83679.
Nat Genet. 2001.
PMID: 11138011
Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation.
Rodriguez D, Gauthier F, Bertini E, Bugiani M, Brenner M, N'guyen S, Goizet C, Gelot A, Surtees R, Pedespan JM, Hernandorena X, Troncoso M, Uziel G, Messing A, Ponsot G, Pham-Dinh D, Dautigny A, Boespflug-Tanguy O.
Rodriguez D, et al.
Am J Hum Genet. 2001 Nov;69(5):1134-40. doi: 10.1086/323799. Epub 2001 Sep 20.
Am J Hum Genet. 2001.
PMID: 11567214
Free PMC article.
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Autophagy induced by Alexander disease-mutant GFAP accumulation is regulated by p38/MAPK and mTOR signaling pathways.
Tang G, Yue Z, Talloczy Z, Hagemann T, Cho W, Messing A, Sulzer DL, Goldman JE.
Tang G, et al.
Hum Mol Genet. 2008 Jun 1;17(11):1540-55. doi: 10.1093/hmg/ddn042. Epub 2008 Feb 14.
Hum Mol Genet. 2008.
PMID: 18276609
Free PMC article.
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