These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
106 related articles for article (PubMed ID: 17030535)
41. Progranulin deficiency induces overactivation of WNT5A expression via TNF-α/NF-κB pathway in peripheral cells from frontotemporal dementia-linked granulin mutation carriers. Alquézar C; de la Encarnación A; Moreno F; López de Munain A; Martín-Requero Á J Psychiatry Neurosci; 2016 Jun; 41(4):225-39. PubMed ID: 26624524 [TBL] [Abstract][Full Text] [Related]
42. A familial form of parkinsonism, dementia, and motor neuron disease: a longitudinal study. Fujioka S; Boeve BF; Parisi JE; Tacik P; Aoki N; Strongosky AJ; Baker M; Sanchez-Contreras M; Ross OA; Rademakers R; Sossi V; Dickson DW; Stoessl AJ; Wszolek ZK Parkinsonism Relat Disord; 2014 Nov; 20(11):1129-34. PubMed ID: 25175602 [TBL] [Abstract][Full Text] [Related]
43. Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration. Chen-Plotkin AS; Geser F; Plotkin JB; Clark CM; Kwong LK; Yuan W; Grossman M; Van Deerlin VM; Trojanowski JQ; Lee VM Hum Mol Genet; 2008 May; 17(10):1349-62. PubMed ID: 18223198 [TBL] [Abstract][Full Text] [Related]
44. Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion. Shankaran SS; Capell A; Hruscha AT; Fellerer K; Neumann M; Schmid B; Haass C J Biol Chem; 2008 Jan; 283(3):1744-1753. PubMed ID: 17984093 [TBL] [Abstract][Full Text] [Related]
45. "Frontotemporoparietal" dementia: clinical phenotype associated with the c.709-1G>A PGRN mutation. Moreno F; Indakoetxea B; Barandiaran M; Alzualde A; Gabilondo A; Estanga A; Ruiz J; Ruibal M; Bergareche A; Martí-Massó JF; López de Munain A Neurology; 2009 Oct; 73(17):1367-74. PubMed ID: 19858458 [TBL] [Abstract][Full Text] [Related]
46. Update on recent molecular and genetic advances in frontotemporal lobar degeneration. Bigio EH J Neuropathol Exp Neurol; 2008 Jul; 67(7):635-48. PubMed ID: 18596549 [TBL] [Abstract][Full Text] [Related]
47. Suppression of Progranulin Expression Leads to Formation of Intranuclear TDP-43 Inclusions In Vitro: A Cell Model of Frontotemporal Lobar Degeneration. Zhu J; Wang N; Li X; Zheng X; Zhao J; Xia H; Mao Q J Neuropathol Exp Neurol; 2019 Dec; 78(12):1124-1129. PubMed ID: 31626287 [TBL] [Abstract][Full Text] [Related]
48. Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation. Skoglund L; Brundin R; Olofsson T; Kalimo H; Ingvast S; Blom ES; Giedraitis V; Ingelsson M; Lannfelt L; Basun H; Glaser A Neurogenetics; 2009 Feb; 10(1):27-34. PubMed ID: 18855025 [TBL] [Abstract][Full Text] [Related]
49. Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutations. Van Deerlin VM; Wood EM; Moore P; Yuan W; Forman MS; Clark CM; Neumann M; Kwong LK; Trojanowski JQ; Lee VM; Grossman M Arch Neurol; 2007 Aug; 64(8):1148-53. PubMed ID: 17698705 [TBL] [Abstract][Full Text] [Related]
50. The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration. Yu CE; Bird TD; Bekris LM; Montine TJ; Leverenz JB; Steinbart E; Galloway NM; Feldman H; Woltjer R; Miller CA; Wood EM; Grossman M; McCluskey L; Clark CM; Neumann M; Danek A; Galasko DR; Arnold SE; Chen-Plotkin A; Karydas A; Miller BL; Trojanowski JQ; Lee VM; Schellenberg GD; Van Deerlin VM Arch Neurol; 2010 Feb; 67(2):161-70. PubMed ID: 20142524 [TBL] [Abstract][Full Text] [Related]
51. Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease. Shiarli AM; Jennings R; Shi J; Bailey K; Davidson Y; Tian J; Bigio EH; Ghetti B; Murrell JR; Delisle MB; Mirra S; Crain B; Zolo P; Arima K; Iseki E; Murayama S; Kretzschmar H; Neumann M; Lippa C; Halliday G; Mackenzie J; Khan N; Ravid R; Dickson D; Wszolek Z; Iwatsubo T; Pickering-Brown SM; Mann DM Neuropathol Appl Neurobiol; 2006 Aug; 32(4):374-87. PubMed ID: 16866983 [TBL] [Abstract][Full Text] [Related]
52. Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration. Chen-Plotkin AS; Martinez-Lage M; Sleiman PM; Hu W; Greene R; Wood EM; Bing S; Grossman M; Schellenberg GD; Hatanpaa KJ; Weiner MF; White CL; Brooks WS; Halliday GM; Kril JJ; Gearing M; Beach TG; Graff-Radford NR; Dickson DW; Rademakers R; Boeve BF; Pickering-Brown SM; Snowden J; van Swieten JC; Heutink P; Seelaar H; Murrell JR; Ghetti B; Spina S; Grafman J; Kaye JA; Woltjer RL; Mesulam M; Bigio E; Lladó A; Miller BL; Alzualde A; Moreno F; Rohrer JD; Mackenzie IR; Feldman HH; Hamilton RL; Cruts M; Engelborghs S; De Deyn PP; Van Broeckhoven C; Bird TD; Cairns NJ; Goate A; Frosch MP; Riederer PF; Bogdanovic N; Lee VM; Trojanowski JQ; Van Deerlin VM Arch Neurol; 2011 Apr; 68(4):488-97. PubMed ID: 21482928 [TBL] [Abstract][Full Text] [Related]