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References

  • Ahmed Z., Mackenzie I. R., Hutton M. L. and Dickson D. W. (2007) Progranulin in frontotemporal lobar degeneration and neuroinflammation. J. Neuroinflammation 4, 7.
  • Baker M., Mackenzie I. R., Pickering-Brown S. M. et al. (2006) Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442, 916919.
  • Bause E. and Legler G. (1981) The role of the hydroxy amino acid in the triplet sequence Asn-Xaa-Thr(Ser) for the N-glycosylation step during glycoprotein biosynthesis. Biochem. J. 195, 639644.
  • Bieniek K. F., Murray M. E., Rutherford N. J. et al. (2013) Tau pathology in frontotemporal lobar degeneration with C9ORF72 hexanucleotide repeat expansion. Acta Neuropathol. 125, 289302.
  • Boxer A. L. and Miller B. L. (2005) Clinical features of frontotemporal dementia. Alzheimer Dis. Assoc. Disord. 19(Suppl 1), S3S6.
  • Brady O. A., Zheng Y., Murphy K., Huang M. and Hu F. (2013) The frontotemporal lobar degeneration risk factor, TMEM106B, regulates lysosomal morphology and function. Hum. Mol. Genet. 22, 685695.
  • Chen-Plotkin A. S., Unger T. L., Gallagher M. D. et al. (2012) TMEM106B, the risk gene for frontotemporal dementia, is regulated by the microRNA-132/212 cluster and affects progranulin pathways. J. Neurosci. 32, 1121311227.
  • Cruchaga C., Graff C., Chiang H. H. et al. (2011) Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels. Arch. Neurol. 68, 581586.
  • Cruts M., Gijselinck I., van der Zee J. et al. (2006) Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 442, 920924.
  • DeJesus-Hernandez M., Mackenzie I. R., Boeve B. F. et al. (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72, 245256.
  • Finch N., Carrasquillo M. M., Baker M. et al. (2011) TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers. Neurology 76, 467474.
  • Gass J., Cannon A., Mackenzie I. R. et al. (2006) Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Hum. Mol. Genet. 15, 29883001.
  • Ghidoni R., Stoppani E., Rossi G. et al. (2012) Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study. Neurodegener. Dis. 9, 121127.
  • Gijselinck I., van der Zee J., Engelborghs S. et al. (2008) Progranulin locus deletion in frontotemporal dementia. Hum. Mutat. 29, 5358.
  • Lang C. M., Fellerer K., Schwenk B. M., Kuhn P. H., Kremmer E., Edbauer D., Capell A. and Haass C. (2012) Membrane orientation and subcellular localization of transmembrane protein 106B (TMEM106B), a major risk factor for frontotemporal lobar degeneration. J. Biol. Chem. 287, 1935519365.
  • McKhann G. M., Albert M. S., Grossman M., Miller B., Dickson D. and Trojanowski J. Q. (2001) Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease. Arch. Neurol. 58, 18031809.
  • Neary D., Snowden J. S., Gustafson L. et al. (1998) Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 51, 15461554.
  • Ratnavalli E., Brayne C., Dawson K. and Hodges J. R. (2002) The prevalence of frontotemporal dementia. Neurology 58, 16151621.
  • Renton A. E., Majounie E., Waite A. et al. (2011) A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 72, 257268.
  • Rutherford N. J., Carrasquillo M. M., Li M. et al. (2012) TMEM106B risk variant is implicated in the pathologic presentation of Alzheimer disease. Neurology 79, 717718.
  • Vass R., Ashbridge E., Geser F. et al. (2011) Risk genotypes at TMEM106B are associated with cognitive impairment in amyotrophic lateral sclerosis. Acta Neuropathol. 121, 373380.
  • Van Deerlin V. M., Sleiman P. M., Martinez-Lage M. et al. (2010) Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nat. Genet. 42, 234239.
  • van der Zee J., Van Langenhove T., Kleinberger G. et al. (2011) TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort. Brain 134, 808815.