1. Duguid, J R JR, Bohmont, C W CW, Liu, N G NG and Tourtellotte, W W WW.. (1989) Changes in brain gene expression shared by scrapie and Alzheimer disease.. Proceedings of the National Academy of Sciences of the United States of America, [PMID:2780570] |
2. Kosako, H H and 6 more authors.. (1997) Phosphorylation of glial fibrillary acidic protein at the same sites by cleavage furrow kinase and Rho-associated kinase.. The Journal of biological chemistry, (18): [PMID:9099667] |
3. Matsuzawa, K K and 10 more authors.. (1997) Domain-specific phosphorylation of vimentin and glial fibrillary acidic protein by PKN.. Biochemical and biophysical research communications, (29): [PMID:9175763] |
4. Isaacs, A A, Baker, M M, Wavrant-De Vrièze, F F and Hutton, M M.. (1998) Determination of the gene structure of human GFAP and absence of coding region mutations associated with frontotemporal dementia with parkinsonism linked to chromosome 17.. Genomics, (1): [PMID:9693047] |
5. Brenner, M M and 5 more authors.. (2001) Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease.. Nature genetics, [PMID:11138011] |
6. Nielsen, Anders Lade AL and 5 more authors.. (2002) A new splice variant of glial fibrillary acidic protein, GFAP epsilon, interacts with the presenilin proteins.. The Journal of biological chemistry, (16): [PMID:12058025] |
7. Kawajiri, Aie A and 6 more authors.. (2003) Functional significance of the specific sites phosphorylated in desmin at cleavage furrow: Aurora-B may phosphorylate and regulate type III intermediate filaments during cytokinesis coordinatedly with Rho-kinase.. Molecular biology of the cell, [PMID:12686604] |
8. Zody, Michael C MC and 73 more authors.. (2006) DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.. Nature, (20): [PMID:16625196] |
9. Lee, Jung Mu and 8 more authors.. (2006) A case of infantile Alexander disease accompanied by infantile spasms diagnosed by DNA analysis.. Journal of Korean medical science, [PMID:17043438] |
10. Hinttala, Reetta R and 5 more authors.. (2007) Alexander disease with occipital predominance and a novel c.799G>C mutation in the GFAP gene.. Acta neuropathologica, [PMID:17805552] |
11. Bechtel, Stephanie S and 18 more authors.. (2007) The full-ORF clone resource of the German cDNA Consortium.. BMC genomics, (31): [PMID:17974005] |
12. Ye Wu and 5 more authors.. (2008) Clinical and genetic study in Chinese patients with Alexander disease.. Journal of child neurology, [PMID:18079314] |
13. Kaneko, Hiroyuki H and 10 more authors.. (2009) Novel GFAP mutation in patient with adult-onset Alexander disease presenting with spastic ataxia.. Movement disorders : official journal of the Movement Disorder Society, (15): [PMID:19412928] |
14. Namekawa, Michito M and 5 more authors.. (2010) Adult-onset Alexander disease with typical "tadpole" brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature.. BMC neurology, (1): [PMID:20359319] |
15. Jin, Zhicheng and 5 more authors.. (2013) Identification and characterization of citrulline-modified brain proteins by combining HCD and CID fragmentation.. Proteomics, [PMID:23828821] |