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Results: 1 to 20 of 246

Similar articles for PubMed (Select 16862115)

1.

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.

Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, Pirici D, Rademakers R, Vandenberghe R, Dermaut B, Martin JJ, van Duijn C, Peeters K, Sciot R, Santens P, De Pooter T, Mattheijssens M, Van den Broeck M, Cuijt I, Vennekens K, De Deyn PP, Kumar-Singh S, Van Broeckhoven C.

Nature. 2006 Aug 24;442(7105):920-4. Epub 2006 Jul 16.

PMID:
16862115
2.

Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation.

Behnam M, Ghorbani F, Shin JH, Kim DS, Jang H, Nouri N, Sedghi M, Salehi M, Ansari B, Basiri K.

Gene. 2015 Jun 15. pii: S0378-1119(15)00741-6. doi: 10.1016/j.gene.2015.06.033. [Epub ahead of print]

PMID:
26086902
3.

The molecular basis for development of proinflammatory autoantibodies to progranulin.

Thurner L, Fadle N, Regitz E, Kemele M, Klemm P, Zaks M, Stöger E, Bette B, Carbon G, Zimmer V, Assmann G, Murawski N, Kubuschok B, Held G, Preuss KD, Pfreundschuh M.

J Autoimmun. 2015 May 21. pii: S0896-8411(15)00062-1. doi: 10.1016/j.jaut.2015.05.002. [Epub ahead of print]

PMID:
26005049
4.

A network of RNA and protein interactions in Fronto Temporal Dementia.

Fontana F, Siva K, Denti MA.

Front Mol Neurosci. 2015 Mar 19;8:9. doi: 10.3389/fnmol.2015.00009. eCollection 2015. Review.

5.

Frontotemporal dementia parkinsonism: Clinical findings in a large Iranian family.

Basiri K, Ansari B, Meamar R.

Adv Biomed Res. 2015 Feb 11;4:37. doi: 10.4103/2277-9175.151242. eCollection 2015.

6.

Cerebral hypometabolism and grey matter density in MAPT intron 10 +3 mutation carriers.

Deters KD, Risacher SL, Farlow MR, Unverzagt FW, Kareken DA, Hutchins GD, Yoder KK, Murrell JR, Spina S, Epperson F, Gao S, Saykin AJ, Ghetti B.

Am J Neurodegener Dis. 2014 Dec 5;3(3):103-14. eCollection 2014.

7.

Restoration of progranulin expression rescues cortical neuron generation in an induced pluripotent stem cell model of frontotemporal dementia.

Raitano S, Ordovàs L, De Muynck L, Guo W, Espuny-Camacho I, Geraerts M, Khurana S, Vanuytsel K, Tóth BI, Voets T, Vandenberghe R, Cathomen T, Van Den Bosch L, Vanderhaeghen P, Van Damme P, Verfaillie CM.

Stem Cell Reports. 2015 Jan 13;4(1):16-24. doi: 10.1016/j.stemcr.2014.12.001. Epub 2014 Dec 31.

8.

Parkinsonian syndrome in familial frontotemporal dementia.

Siuda J, Fujioka S, Wszolek ZK.

Parkinsonism Relat Disord. 2014 Sep;20(9):957-64. doi: 10.1016/j.parkreldis.2014.06.004. Epub 2014 Jun 13.

9.

Progranulin in neurodegenerative disease.

Petkau TL, Leavitt BR.

Trends Neurosci. 2014 Jul;37(7):388-98. doi: 10.1016/j.tins.2014.04.003. Epub 2014 May 4. Review.

PMID:
24800652
10.

Targeted manipulation of the sortilin-progranulin axis rescues progranulin haploinsufficiency.

Lee WC, Almeida S, Prudencio M, Caulfield TR, Zhang YJ, Tay WM, Bauer PO, Chew J, Sasaguri H, Jansen-West KR, Gendron TF, Stetler CT, Finch N, Mackenzie IR, Rademakers R, Gao FB, Petrucelli L.

Hum Mol Genet. 2014 Mar 15;23(6):1467-78. doi: 10.1093/hmg/ddt534. Epub 2013 Oct 26.

11.

Activity-dependent secretion of progranulin from synapses.

Petoukhov E, Fernando S, Mills F, Shivji F, Hunter D, Krieger C, Silverman MA, Bamji SX.

J Cell Sci. 2013 Dec 1;126(Pt 23):5412-21. doi: 10.1242/jcs.132076. Epub 2013 Sep 17.

12.

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. doi: 10.1159/000352022. Epub 2013 Sep 6.

PMID:
24022032
13.

Imaging prodromal FTD: seeing the future through PET crystals.

Rabinovici GD, Boeve BF.

Neurology. 2013 Oct 8;81(15):1282-3. doi: 10.1212/WNL.0b013e3182a82591. Epub 2013 Sep 4. No abstract available.

PMID:
24005338
14.

Potential roles of microglial cell progranulin in HIV-associated CNS pathologies and neurocognitive impairment.

Suh HS, Gelman BB, Lee SC.

J Neuroimmune Pharmacol. 2014 Mar;9(2):117-32. Review.

15.

Novel progranulin variants do not disrupt progranulin secretion and cleavage.

Karch CM, Jeng AT, Skorupa T, Cruchaga C, Goate AM.

Neurobiol Aging. 2013 Nov;34(11):2538-40. doi: 10.1016/j.neurobiolaging.2013.05.004. Epub 2013 Jun 4.

16.

Mechanisms of granulin deficiency: lessons from cellular and animal models.

Kleinberger G, Capell A, Haass C, Van Broeckhoven C.

Mol Neurobiol. 2013 Feb;47(1):337-60. doi: 10.1007/s12035-012-8380-8. Epub 2012 Dec 13. Review.

17.

Neuropsychological features of asymptomatic c.709-1G>A progranulin mutation carriers.

Barandiaran M, Estanga A, Moreno F, Indakoetxea B, Alzualde A, Balluerka N, Martí Massó JF, López de Munain A.

J Int Neuropsychol Soc. 2012 Nov;18(6):1086-90. doi: 10.1017/S1355617712000823.

PMID:
23158232
18.

Induced pluripotent stem cell models of progranulin-deficient frontotemporal dementia uncover specific reversible neuronal defects.

Almeida S, Zhang Z, Coppola G, Mao W, Futai K, Karydas A, Geschwind MD, Tartaglia MC, Gao F, Gianni D, Sena-Esteves M, Geschwind DH, Miller BL, Farese RV Jr, Gao FB.

Cell Rep. 2012 Oct 25;2(4):789-98. doi: 10.1016/j.celrep.2012.09.007. Epub 2012 Oct 11.

19.

Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS.

Ogaki K, Li Y, Takanashi M, Ishikawa K, Kobayashi T, Nonaka T, Hasegawa M, Kishi M, Yoshino H, Funayama M, Tsukamoto T, Shioya K, Yokochi M, Imai H, Sasaki R, Kokubo Y, Kuzuhara S, Motoi Y, Tomiyama H, Hattori N.

Parkinsonism Relat Disord. 2013 Jan;19(1):15-20. doi: 10.1016/j.parkreldis.2012.06.019. Epub 2012 Jul 18.

PMID:
22818528
20.

Recent insights into the involvement of progranulin in frontotemporal dementia.

Sun L, Eriksen JL.

Curr Neuropharmacol. 2011 Dec;9(4):632-42. doi: 10.2174/157015911798376361.

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