176 related articles for article (PubMed ID: 23724906)
41. 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]
42. Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.
Le Ber I; Camuzat A; Hannequin D; Pasquier F; Guedj E; Rovelet-Lecrux A; Hahn-Barma V; van der Zee J; Clot F; Bakchine S; Puel M; Ghanim M; Lacomblez L; Mikol J; Deramecourt V; Lejeune P; de la Sayette V; Belliard S; Vercelletto M; Meyrignac C; Van Broeckhoven C; Lambert JC; Verpillat P; Campion D; Habert MO; Dubois B; Brice A;
Brain; 2008 Mar; 131(Pt 3):732-46. PubMed ID: 18245784
[TBL] [Abstract][Full Text] [Related]
43. 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]
44. GRN-/- iPSC-derived cortical neurons recapitulate the pathological findings of both frontotemporal lobar degeneration and neuronal ceroidolipofuscinosis.
Bossolasco P; Cimini S; Maderna E; Bardelli D; Canafoglia L; Cavallaro T; Ricci M; Silani V; Marucci G; Rossi G
Neurobiol Dis; 2022 Dec; 175():105891. PubMed ID: 36220610
[TBL] [Abstract][Full Text] [Related]
45. Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma.
Carrasquillo MM; Nicholson AM; Finch N; Gibbs JR; Baker M; Rutherford NJ; Hunter TA; DeJesus-Hernandez M; Bisceglio GD; Mackenzie IR; Singleton A; Cookson MR; Crook JE; Dillman A; Hernandez D; Petersen RC; Graff-Radford NR; Younkin SG; Rademakers R
Am J Hum Genet; 2010 Dec; 87(6):890-7. PubMed ID: 21087763
[TBL] [Abstract][Full Text] [Related]
46. Serum C-Peptide, Visfatin, Resistin, and Ghrelin are Altered in Sporadic and GRN-Associated Frontotemporal Lobar Degeneration.
Zanardini R; Benussi L; Fostinelli S; Saraceno C; Ciani M; Borroni B; Padovani A; Binetti G; Ghidoni R
J Alzheimers Dis; 2018; 61(3):1053-1060. PubMed ID: 29226876
[TBL] [Abstract][Full Text] [Related]
47. Progranulin peripheral levels as a screening tool for the identification of subjects with progranulin mutations in a Portuguese cohort.
Almeida MR; Baldeiras I; Ribeiro MH; Santiago B; Machado C; Massano J; Guimarães J; Resende Oliveira C; Santana I
Neurodegener Dis; 2014; 13(4):214-23. PubMed ID: 24022032
[TBL] [Abstract][Full Text] [Related]
48. Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.
Van Langenhove T; van der Zee J; Gijselinck I; Engelborghs S; Vandenberghe R; Vandenbulcke M; De Bleecker J; Sieben A; Versijpt J; Ivanoiu A; Deryck O; Willems C; Dillen L; Philtjens S; Maes G; Bäumer V; Van Den Broeck M; Mattheijssens M; Peeters K; Martin JJ; Michotte A; Santens P; De Jonghe P; Cras P; De Deyn PP; Cruts M; Van Broeckhoven C
JAMA Neurol; 2013 Mar; 70(3):365-73. PubMed ID: 23338682
[TBL] [Abstract][Full Text] [Related]
49. Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration.
Clot F; Rovelet-Lecrux A; Lamari F; Noël S; Keren B; Camuzat A; Michon A; Jornea L; Laudier B; de Septenville A; Caroppo P; Campion D; Cazeneuve C; Brice A; LeGuern E; Le Ber I;
Neurogenetics; 2014 May; 15(2):95-100. PubMed ID: 24469240
[TBL] [Abstract][Full Text] [Related]
50. Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia.
Wilke C; Gillardon F; Deuschle C; Hobert MA; Jansen IE; Metzger FG; Heutink P; Gasser T; Maetzler W; Blauwendraat C; Synofzik M
Neurodegener Dis; 2017; 17(2-3):83-88. PubMed ID: 27760429
[TBL] [Abstract][Full Text] [Related]
51. GRN variability contributes to sporadic frontotemporal lobar degeneration.
Galimberti D; Fenoglio C; Cortini F; Serpente M; Venturelli E; Villa C; Clerici F; Marcone A; Benussi L; Ghidoni R; Gallone S; Scalabrini D; Restelli I; Martinelli Boneschi F; Cappa S; Binetti G; Mariani C; Rainero I; Giordana MT; Bresolin N; Scarpini E
J Alzheimers Dis; 2010; 19(1):171-7. PubMed ID: 20061636
[TBL] [Abstract][Full Text] [Related]
52. Promoter DNA methylation regulates progranulin expression and is altered in FTLD.
Banzhaf-Strathmann J; Claus R; Mücke O; Rentzsch K; van der Zee J; Engelborghs S; De Deyn PP; Cruts M; van Broeckhoven C; Plass C; Edbauer D
Acta Neuropathol Commun; 2013 May; 1():16. PubMed ID: 24252647
[TBL] [Abstract][Full Text] [Related]
53. Role of progranulin as a biomarker for Alzheimer's disease.
Sleegers K; Brouwers N; Van Broeckhoven C
Biomark Med; 2010 Feb; 4(1):37-50. PubMed ID: 20387302
[TBL] [Abstract][Full Text] [Related]
54. Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy.
Bagnoli S; Piaceri I; Tedde A; Piacentini S; Nannucci S; Bracco L; Sorbi S; Nacmias B
Cell Mol Neurobiol; 2012 Jan; 32(1):13-6. PubMed ID: 21800185
[TBL] [Abstract][Full Text] [Related]
55. Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration.
Krüger J; Kaivorinne AL; Udd B; Majamaa K; Remes AM
Eur J Neurol; 2009 Jan; 16(1):27-30. PubMed ID: 19049508
[TBL] [Abstract][Full Text] [Related]
56. Missense mutations in progranulin gene associated with frontotemporal lobar degeneration: study of pathogenetic features.
Karch CM; Ezerskiy L; Redaelli V; Giovagnoli AR; Tiraboschi P; Pelliccioni G; Pelliccioni P; Kapetis D; D'Amato I; Piccoli E; Ferretti MG; Tagliavini F; Rossi G
Neurobiol Aging; 2016 Feb; 38():215.e1-215.e12. PubMed ID: 26652843
[TBL] [Abstract][Full Text] [Related]
57. Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred.
Pietroboni AM; Fumagalli GG; Ghezzi L; Fenoglio C; Cortini F; Serpente M; Cantoni C; Rotondo E; Corti P; Carecchio M; Bassi M; Bresolin N; Galbiati D; Galimberti D; Scarpini E
J Alzheimers Dis; 2011; 24(2):253-9. PubMed ID: 21258152
[TBL] [Abstract][Full Text] [Related]
58. Novel GRN Mutations in Patients with Corticobasal Syndrome.
Taghdiri F; Sato C; Ghani M; Moreno D; Rogaeva E; Tartaglia MC
Sci Rep; 2016 Mar; 6():22913. PubMed ID: 26961809
[TBL] [Abstract][Full Text] [Related]
59. Progranulin expression in the developing and adult murine brain.
Petkau TL; Neal SJ; Orban PC; MacDonald JL; Hill AM; Lu G; Feldman HH; Mackenzie IR; Leavitt BR
J Comp Neurol; 2010 Oct; 518(19):3931-47. PubMed ID: 20737593
[TBL] [Abstract][Full Text] [Related]
60. Serum biomarker for progranulin-associated frontotemporal lobar degeneration.
Sleegers K; Brouwers N; Van Damme P; Engelborghs S; Gijselinck I; van der Zee J; Peeters K; Mattheijssens M; Cruts M; Vandenberghe R; De Deyn PP; Robberecht W; Van Broeckhoven C
Ann Neurol; 2009 May; 65(5):603-9. PubMed ID: 19288468
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
