Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration

[1]  Houeto Jean-Luc.  [Parkinson's disease]. , 2022, La Revue du praticien.

[2]  E. Rogaeva,et al.  Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis , 2008, Neurobiology of Aging.

[3]  S. Pickering-Brown,et al.  The complex aetiology of frontotemporal lobar degeneration , 2007, Experimental Neurology.

[4]  J. Schneider,et al.  Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration , 2007, Acta Neuropathologica.

[5]  S. Melquist,et al.  Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. , 2006, Human molecular genetics.

[6]  Bruce L. Miller,et al.  Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis , 2006, Science.

[7]  Julie S. Snowden,et al.  Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype , 2006, Acta Neuropathologica.

[8]  S. Melquist,et al.  Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 , 2006, Nature.

[9]  H. Horvitz,et al.  A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia , 2006, Neurology.

[10]  S. Gabriel,et al.  Efficiency and power in genetic association studies , 2005, Nature Genetics.

[11]  Holger Hummerich,et al.  Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia , 2005, Nature Genetics.

[12]  Mark Daly,et al.  Haploview: analysis and visualization of LD and haplotype maps , 2005, Bioinform..

[13]  A. Singleton,et al.  The law of mass action applied to neurodegenerative disease: a hypothesis concerning the etiology and pathogenesis of complex diseases. , 2004, Human molecular genetics.

[14]  A. Pestronk,et al.  Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein , 2004, Nature Genetics.

[15]  L. Petrucelli,et al.  Mechanism of neurodegenerative disease: role of the ubiquitin proteasome system , 2004, Annals of medicine.

[16]  Peter Donnelly,et al.  A comparison of bayesian methods for haplotype reconstruction from population genotype data. , 2003, American journal of human genetics.

[17]  John D. Storey,et al.  Statistical significance for genomewide studies , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[18]  H. Akiyama,et al.  Neuronal and glial inclusions in frontotemporal dementia with or without motor neuron disease are immunopositive for p62 , 2003, Neuroscience Letters.

[19]  S. Gabriel,et al.  The Structure of Haplotype Blocks in the Human Genome , 2002, Science.

[20]  J. Hardy,et al.  Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene. , 2002, Brain : a journal of neurology.

[21]  Z. Zeng,et al.  Isolation and characterization of a novel cDNA, UBAP1, derived from the tumor suppressor locus in human chromosome 9p21–22 , 2001, Journal of Cancer Research and Clinical Oncology.

[22]  P. Donnelly,et al.  A new statistical method for haplotype reconstruction from population data. , 2001, American journal of human genetics.

[23]  R. Faber,et al.  Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. , 1999, Neurology.

[24]  Ronald C. Petersen,et al.  Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 , 1998, Nature.

[25]  D. Curtis,et al.  Monte Carlo tests for associations between disease and alleles at highly polymorphic loci , 1995, Annals of human genetics.

[26]  A. Singleton,et al.  Suppression of MMP-9 by doxycycline in brain arteriovenous malformations , 2004, BMC neurology.

[27]  A Ciechanover,et al.  The ubiquitin-proteasome pathway and pathogenesis of human diseases. , 1999, Annual review of medicine.

[28]  J. Mcleod,et al.  Familial amyotrophic lateral sclerosis. , 1973, Proceedings of the Australian Association of Neurologists.