TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions

Author:

Gallagher Michael D.,Suh Eunran,Grossman Murray,Elman Lauren,McCluskey Leo,Van Swieten John C.,Al-Sarraj Safa,Neumann Manuela,Gelpi Ellen,Ghetti Bernardino,Rohrer Jonathan D.,Halliday Glenda,Van Broeckhoven Christine,Seilhean Danielle,Shaw Pamela J.,Frosch Matthew P.,Alafuzoff Irina,Antonell Anna,Bogdanovic Nenad,Brooks William,Cairns Nigel J.,Cooper-Knock Johnathan,Cotman Carl,Cras Patrick,Cruts Marc,De Deyn Peter P.,DeCarli Charles,Dobson-Stone Carol,Engelborghs Sebastiaan,Fox Nick,Galasko Douglas,Gearing Marla,Gijselinck Ilse,Grafman Jordan,Hartikainen Päivi,Hatanpaa Kimmo J.,Highley J. Robin,Hodges John,Hulette Christine,Ince Paul G.,Jin Lee-Way,Kirby Janine,Kofler Julia,Kril Jillian,Kwok John B. J.,Levey Allan,Lieberman Andrew,Llado Albert,Martin Jean-Jacques,Masliah Eliezer,McDermott Christopher J.,McKee Ann,McLean Catriona,Mead Simon,Miller Carol A.,Miller Josh,Munoz David G.,Murrell Jill,Paulson Henry,Piguet Olivier,Rossor Martin,Sanchez-Valle Raquel,Sano Mary,Schneider Julie,Silbert Lisa C.,Spina Salvatore,van der Zee Julie,Van Langenhove Tim,Warren Jason,Wharton Stephen B.,White III Charles L.,Woltjer Randall L.,Trojanowski John Q.,Lee Virginia M. Y.,Van Deerlin Vivianna,Chen-Plotkin Alice S.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Reference45 articles.

1. Ash PE, Bieniek KF, Gendron TF, Caulfield T, Lin WL, Dejesus-Hernandez M, van Blitterswijk MM, Jansen-West K, Paul JW 3rd, Rademakers R, Boylan KB, Dickson DW, Petrucelli L (2013) Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS. Neuron 77:639–646. doi: 10.1016/j.neuron.2013.02.004

2. Boxer AL, Mackenzie IR, Boeve BF, Baker M, Seeley WW, Crook R, Feldman H, Hsiung GY, Rutherford N, Laluz V, Whitwell J, Foti D, McDade E, Molano J, Karydas A, Wojtas A, Goldman J, Mirsky J, Sengdy P, Dearmond S, Miller BL, Rademakers R (2011) Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD–ALS family. J Neurol Neurosurg Psychiatry 82:196–203. doi: 10.1136/jnnp.2009.204081

3. Brady OA, Zheng Y, Murphy K, Huang M, Hu F (2013) The frontotemporal lobar degeneration risk factor, TMEM106B, regulates lysosomal morphology and function. Hum Mol Genet 22:685–695. doi: 10.1093/hmg/dds475

4. Brooks BR, Miller RG, Swash M, Munsat TL, World Federation of Neurology Research Group on Motor Neuron Diseases (2000) El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord 1:293–299

5. Chen-Plotkin AS, Unger TL, Gallagher MD, Bill E, Kwong LK, Volpicelli-Daley L, Busch JI, Akle S, Grossman M, Van Deerlin V, Trojanowski JQ, Lee VM (2012) TMEM106B, the risk gene for frontotemporal dementia, is regulated by the microRNA-132/212 cluster and affects progranulin pathways. J Neurosci 32:11213–11227. doi: 10.1523/JNEUROSCI.0521-12.2012

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