Hallupp M - Search Results

1

Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies.

Stanford PM, Brooks WS, Teber ET, Hallupp M, McLean C, Halliday GM, Martins RN, Kwok JB, Schofield PR. Stanford PM, et al. Among authors: hallupp m. J Neurol. 2004 Sep;251(9):1098-104. doi: 10.1007/s00415-004-0489-x. J Neurol. 2004. PMID: 15372253

2

Tau haplotypes regulate transcription and are associated with Parkinson's disease.

Kwok JB, Teber ET, Loy C, Hallupp M, Nicholson G, Mellick GD, Buchanan DD, Silburn PA, Schofield PR. Kwok JB, et al. Among authors: hallupp m. Ann Neurol. 2004 Mar;55(3):329-34. doi: 10.1002/ana.10826. Ann Neurol. 2004. PMID: 14991810

3

GSK3B polymorphisms alter transcription and splicing in Parkinson's disease.

Kwok JB, Hallupp M, Loy CT, Chan DK, Woo J, Mellick GD, Buchanan DD, Silburn PA, Halliday GM, Schofield PR. Kwok JB, et al. Among authors: hallupp m. Ann Neurol. 2005 Dec;58(6):829-39. doi: 10.1002/ana.20691. Ann Neurol. 2005. PMID: 16315267

4

Glycogen synthase kinase-3beta and tau genes interact in Alzheimer's disease.

Kwok JB, Loy CT, Hamilton G, Lau E, Hallupp M, Williams J, Owen MJ, Broe GA, Tang N, Lam L, Powell JF, Lovestone S, Schofield PR. Kwok JB, et al. Among authors: hallupp m. Ann Neurol. 2008 Oct;64(4):446-54. doi: 10.1002/ana.21476. Ann Neurol. 2008. PMID: 18991351

5

C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts.

Dobson-Stone C, Hallupp M, Bartley L, Shepherd CE, Halliday GM, Schofield PR, Hodges JR, Kwok JB. Dobson-Stone C, et al. Among authors: hallupp m. Neurology. 2012 Sep 4;79(10):995-1001. doi: 10.1212/WNL.0b013e3182684634. Epub 2012 Aug 8. Neurology. 2012. PMID: 22875086 Free PMC article.

6

Endogenous progesterone levels and frontotemporal dementia: modulation of TDP-43 and Tau levels in vitro and treatment of the A315T TARDBP mouse model.

Dang TN, Dobson-Stone C, Glaros EN, Kim WS, Hallupp M, Bartley L, Piguet O, Hodges JR, Halliday GM, Double KL, Schofield PR, Crouch PJ, Kwok JB. Dang TN, et al. Among authors: hallupp m. Dis Model Mech. 2013 Sep;6(5):1198-204. doi: 10.1242/dmm.011460. Epub 2013 Jun 20. Dis Model Mech. 2013. PMID: 23798570 Free PMC article.

7

Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies.

Forrest SL, Kril JJ, Stevens CH, Kwok JB, Hallupp M, Kim WS, Huang Y, McGinley CV, Werka H, Kiernan MC, Götz J, Spillantini MG, Hodges JR, Ittner LM, Halliday GM. Forrest SL, et al. Among authors: hallupp m. Brain. 2018 Feb 1;141(2):521-534. doi: 10.1093/brain/awx328. Brain. 2018. PMID: 29253099 Free PMC article.

8

Presenilin-1 mutation L271V results in altered exon 8 splicing and Alzheimer's disease with non-cored plaques and no neuritic dystrophy.

Kwok JB, Halliday GM, Brooks WS, Dolios G, Laudon H, Murayama O, Hallupp M, Badenhop RF, Vickers J, Wang R, Naslund J, Takashima A, Gandy SE, Schofield PR. Kwok JB, et al. Among authors: hallupp m. J Biol Chem. 2003 Feb 28;278(9):6748-54. doi: 10.1074/jbc.M211827200. Epub 2002 Dec 19. J Biol Chem. 2003. PMID: 12493737 Free article.

9

No association of spastic paraparesis genes in PSEN1 Alzheimer's disease with spastic paraparesis.

Karlstrom H, Kwok JB, Gregory GC, Hallupp M, Brooks WS, Schofield PR. Karlstrom H, et al. Among authors: hallupp m. Neuroreport. 2007 Aug 6;18(12):1267-9. doi: 10.1097/WNR.0b013e3282405209. Neuroreport. 2007. PMID: 17632280

10

C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients.

Dobson-Stone C, Hallupp M, Loy CT, Thompson EM, Haan E, Sue CM, Panegyres PK, Razquin C, Seijo-Martínez M, Rene R, Gascon J, Campdelacreu J, Schmoll B, Volk AE, Brooks WS, Schofield PR, Pastor P, Kwok JB. Dobson-Stone C, et al. Among authors: hallupp m. PLoS One. 2013;8(2):e56899. doi: 10.1371/journal.pone.0056899. Epub 2013 Feb 20. PLoS One. 2013. PMID: 23437264 Free PMC article.

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