Frontotemporal dementia and amyotrophic lateral sclerosis-associated disease protein TDP-43 promotes dendritic branching

[1] Boxer AL(2005)Clinical features of frontotemporal dementia Alzheimer Dis Assoc Disord 19 S3-6

[2] Miller BL(2008)New approaches to the treatment of frontotemporal lobar degeneration Curr Opin Neurol 21 708-716

[3] Vossel KA(1998)Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17 Science 282 1914-1917

[4] Miller BL(1998)Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17 Nature 393 702-705

[5] Hong M(2004)Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein Nat Genet 36 377-381

[6] Zhukareva V(2005)Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia Nat Genet 37 806-808

[7] Vogelsberg-Ragaglia V(2006)Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 Nature 442 916-919

[8] Wszolek Z(2006)Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 Nature 442 920-924

[9] Reed L(2006)Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis Science 314 130-133

[10] Miller BI(2006)TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis Biochem Biophys Res Commun 351 602-611

[1] Boxer AL(2005)Clinical features of frontotemporal dementia Alzheimer Dis Assoc Disord 19 S3-6

[2] Miller BL(2008)New approaches to the treatment of frontotemporal lobar degeneration Curr Opin Neurol 21 708-716

[3] Vossel KA(1998)Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17 Science 282 1914-1917

[4] Miller BL(1998)Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17 Nature 393 702-705

[5] Hong M(2004)Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein Nat Genet 36 377-381

[6] Zhukareva V(2005)Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia Nat Genet 37 806-808

[7] Vogelsberg-Ragaglia V(2006)Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 Nature 442 916-919

[8] Wszolek Z(2006)Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 Nature 442 920-924

[9] Reed L(2006)Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis Science 314 130-133

[10] Miller BI(2006)TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis Biochem Biophys Res Commun 351 602-611