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Marc Cruts

Showing results (61-70 of 85) with videos related to

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Scientific Reports|February 13, 2016
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTDSteven Boeynaems, Elke Bogaert, Emiel Michiels, et al.
Neurology|November 20, 2015
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohortIlse Gijselinck, Sara Van Mossevelde, Julie van der Zee, et al.
Nature|July 25, 2006
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21Marc Cruts, Ilse Gijselinck, Julie van der Zee, et al.
Brain : a Journal of Neurology|December 18, 2015
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohortSara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
Human Mutation|April 17, 2007
Progranulin null mutations in both sporadic and familial frontotemporal dementiaIsabelle Le Ber, Julie van der Zee, Didier Hannequin, et al.
Acta Neuropathologica Communications|November 12, 2015
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brainsJonathan Janssens, Stéphanie Philtjens, Gernot Kleinberger, et al.
Human Mutation|March 9, 2007
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementiaJulie van der Zee, Isabelle Le Ber, Sebastian Maurer-Stroh, et al.
Neurobiology of Aging|April 14, 2018
Clinical variability and onset age modifiers in an extended Belgian GRN founder familyEline Wauters, Sara Van Mossevelde, Kristel Sleegers, et al.
Archives of Neurology|October 10, 2007
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder familyNathalie Brouwers, Karen Nuytemans, Julie van der Zee, et al.
Genome Research|September 27, 2007
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21Robert Lyle, Paola Prandini, Kazutoyo Osoegawa, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
Scientific Reports|February 13, 2016
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTDSteven Boeynaems, Elke Bogaert, Emiel Michiels, et al.
Neurology|November 20, 2015
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohortIlse Gijselinck, Sara Van Mossevelde, Julie van der Zee, et al.
Nature|July 25, 2006
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21Marc Cruts, Ilse Gijselinck, Julie van der Zee, et al.
Brain : a Journal of Neurology|December 18, 2015
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohortSara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
Human Mutation|April 17, 2007
Progranulin null mutations in both sporadic and familial frontotemporal dementiaIsabelle Le Ber, Julie van der Zee, Didier Hannequin, et al.
Acta Neuropathologica Communications|November 12, 2015
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brainsJonathan Janssens, Stéphanie Philtjens, Gernot Kleinberger, et al.
Human Mutation|March 9, 2007
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementiaJulie van der Zee, Isabelle Le Ber, Sebastian Maurer-Stroh, et al.
Neurobiology of Aging|April 14, 2018
Clinical variability and onset age modifiers in an extended Belgian GRN founder familyEline Wauters, Sara Van Mossevelde, Kristel Sleegers, et al.
Archives of Neurology|October 10, 2007
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder familyNathalie Brouwers, Karen Nuytemans, Julie van der Zee, et al.
Genome Research|September 27, 2007
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21Robert Lyle, Paola Prandini, Kazutoyo Osoegawa, et al.
Pageof 9