Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

Author： Gass Jennifer   Cannon Ashley   Boeve Bradley   Baker Matt   Adamson Jennifer   Crook Richard   Melquist Stacey   Kuntz Karen   Petersen Ron   Josephs Keith   Pickering-Brown Stuart M.   Graff-Radford Neill   Uitti Ryan   Dickson Dennis   Wszolek Zbigniew   Gonzalez John   Beach Thomas G.   Bigio Eileen   Johnson Nancy   Weintraub Sandra   Mesulam Marsel   White Charles L.   Woodruff Bryan   Caselli Richard   Hsiung Ging-Yuek   Feldman Howard   Knopman Dave   Hutton Mike   Rademakers Rosa  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.15, Iss.20, 2006-10, pp. : 2988-3001

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration

By Chen-Plotkin Alice S.   Geser Felix   Plotkin Joshua B.   Clark Chris M.   Kwong Linda K.   Yuan Wuxing   Grossman Murray   Van Deerlin Vivianna M.   Trojanowski John Q.   Lee Virginia M.-Y.  

Human Molecular Genetics, Vol. 17, Iss. 10, 2008-05 ,pp. : 1349-1362

Oxford University Press

Access to resources Recommend Favorite

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro

By van der Zee Julie   Urwin Hazel   Engelborghs Sebastiaan   Bruyland Marc   Vandenberghe Rik   Dermaut Bart   De Pooter Tim   Peeters Karin   Santens Patrick   De Deyn Peter P.   Fisher Elizabeth M.   Collinge John   Isaacs Adrian M.   Van Broeckhoven Christine  

Human Molecular Genetics, Vol. 17, Iss. 2, 2008-01 ,pp. : 313-322

Oxford University Press

Access to resources Recommend Favorite

The frontotemporal lobar degeneration risk factor, TMEM106B, regulates lysosomal morphology and function

By Brady Owen A.   Zheng Yanqiu   Murphy Kira   Huang Marshall   Hu Fenghua  

Human Molecular Genetics, Vol. 22, Iss. 4, 2013-02 ,pp. : 685-695

Oxford University Press

Access to resources Recommend Favorite

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome

By Tassone F.  

Human Molecular Genetics, Vol. 12, Iss. 9, 2003-05 ,pp. : 949-959

Oxford University Press

Access to resources Recommend Favorite

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

By Rademakers Rosa   Eriksen Jason L.   Baker Matt   Robinson Todd   Ahmed Zeshan   Lincoln Sarah J.   Finch Nicole   Rutherford Nicola J.   Crook Richard J.   Josephs Keith A.   Boeve Bradley F.   Knopman David S.   Petersen Ronald C.   Parisi Joseph E.   Caselli Richard J.   Wszolek Zbigniew K.   Uitti Ryan J.   Feldman Howard   Hutton Michael L.   Mackenzie Ian R.   Graff-Radford Neill R.   Dickson Dennis W.  

Human Molecular Genetics, Vol. 17, Iss. 23, 2008-12 ,pp. : 3631-3642

Oxford University Press

Access to resources Recommend Favorite