Literature DB >> 14595660

An English kindred with a novel recessive tauopathy and respiratory failure.

David J Nicholl1, Michael A Greenstone, Carl E Clarke, Patrizia Rizzu, Daniel Crooks, Alex Crowe, John Q Trojanowski, Virginia M-Y Lee, Peter Heutink.   

Abstract

We present the clinicopathological features of two siblings from a consanguineous marriage who presented with respiratory hypoventilation and died 10 days and 4 years later, respectively. This disorder showed extensive tau neuropathology, and both had a novel homozygous S352L tau gene mutation. This is the first description of a pathologically proved young-onset tauopathy with apparent recessive inheritance.

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Year:  2003        PMID: 14595660     DOI: 10.1002/ana.10747

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  16 in total

1.  A Conserved Cytoskeletal Signaling Cascade Mediates Neurotoxicity of FTDP-17 Tau Mutations In Vivo.

Authors:  Farah H Bardai; Liqun Wang; Yamini Mutreja; Mythili Yenjerla; T Chris Gamblin; Mel B Feany
Journal:  J Neurosci       Date:  2017-11-14       Impact factor: 6.167

2.  Central hypoventilation in progressive supranuclear palsy.

Authors:  Kory S Herrick; Randy Woltjer; Thao Pham; Megan Chalupsky; Amie L Hiller
Journal:  Mov Disord Clin Pract       Date:  2016-05-19

Review 3.  The cytoskeleton in neurodegenerative diseases.

Authors:  Nigel J Cairns; Virginia M-Y Lee; John Q Trojanowski
Journal:  J Pathol       Date:  2004-11       Impact factor: 7.996

4.  Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by MAPT Variants.

Authors:  Laura Williams; Diana A Olszewska; Conor Fearon; Brian Magennis; Allan McCarthy; Lewis P Rowland; Richard Mayeux; Rory Page; Stanley Fahn; Alan Beausang; Tim Lynch
Journal:  Mov Disord Clin Pract       Date:  2021-06-24

5.  FTD-associated mutations in Tau result in a combination of dominant and recessive phenotypes.

Authors:  Alexander D Law; Marlène Cassar; Dani M Long; Eileen S Chow; Jadwiga M Giebultowicz; Anjana Venkataramanan; Roland Strauss; Doris Kretzschmar
Journal:  Neurobiol Dis       Date:  2022-05-16       Impact factor: 7.046

6.  Impaired tau-microtubule interactions are prevalent among pathogenic tau variants arising from missense mutations.

Authors:  Yuxing Xia; Zachary A Sorrentino; Justin D Kim; Kevin H Strang; Cara J Riffe; Benoit I Giasson
Journal:  J Biol Chem       Date:  2019-10-24       Impact factor: 5.157

Review 7.  Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging.

Authors:  B Ghetti; A L Oblak; B F Boeve; K A Johnson; B C Dickerson; M Goedert
Journal:  Neuropathol Appl Neurobiol       Date:  2015-02       Impact factor: 8.090

8.  Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.

Authors:  Gil-Mi Ryu; Pamela Song; Kyu-Won Kim; Kyung-Soo Oh; Keun-Joon Park; Jong Hun Kim
Journal:  Nucleic Acids Res       Date:  2009-01-12       Impact factor: 16.971

Review 9.  Frontotemporal lobar degeneration: old knowledge and new insight into the pathogenetic mechanisms of tau mutations.

Authors:  Giacomina Rossi; Fabrizio Tagliavini
Journal:  Front Aging Neurosci       Date:  2015-10-14       Impact factor: 5.750

10.  The homologous carboxyl-terminal domains of microtubule-associated protein 2 and TAU induce neuronal dysfunction and have differential fates in the evolution of neurofibrillary tangles.

Authors:  Ce Xie; Tomohiro Miyasaka; Satomi Yoshimura; Hiroyuki Hatsuta; Sawako Yoshina; Eriko Kage-Nakadai; Shohei Mitani; Shigeo Murayama; Yasuo Ihara
Journal:  PLoS One       Date:  2014-02-25       Impact factor: 3.240

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