Literature DB >> 15452312

Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegia.

M Fichera1, M Lo Giudice, M Falco, M Sturnio, S Amata, O Calabrese, S Bigoni, E Calzolari, M Neri.   

Abstract

Hereditary spastic paraplegias (HSPs) are characterized by progressive lower extremity spasticity due to an axonal degeneration of motor and sensory neurons. We report a four-generation pedigree segregating an autosomal dominant phenotype for HSP and showing a linkage to the SPG10 locus, coding for Kinesin family member 5A. Subsequent to a denaturing high performance liquid chromatography (dHPLC) mutation screening we found a new missense mutation 838C>T (R280C) at an invariant arginine residue in a region involved in the microtubule binding activity.

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Year:  2004        PMID: 15452312     DOI: 10.1212/01.wnl.0000138731.60693.d2

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  44 in total

1.  Kinesin is an evolutionarily fine-tuned molecular ratchet-and-pawl device of decisively locked direction.

Authors:  Zhisong Wang; Min Feng; Wenwei Zheng; Dagong Fan
Journal:  Biophys J       Date:  2007-08-03       Impact factor: 4.033

2.  Impairments in fast axonal transport and motor neuron deficits in transgenic mice expressing familial Alzheimer's disease-linked mutant presenilin 1.

Authors:  Orly Lazarov; Gerardo A Morfini; Gustavo Pigino; Archana Gadadhar; Xiangjun Chen; John Robinson; Hanson Ho; Scott T Brady; Sangram S Sisodia
Journal:  J Neurosci       Date:  2007-06-27       Impact factor: 6.167

3.  A history of mitochondrial diseases.

Authors:  Salvatore Dimauro
Journal:  J Inherit Metab Dis       Date:  2010-05-21       Impact factor: 4.982

4.  Genetic Basis of Common Human Disease: Insight into the Role of Missense SNPs from Genome-Wide Association Studies.

Authors:  Lipika R Pal; John Moult
Journal:  J Mol Biol       Date:  2015-05-01       Impact factor: 5.469

5.  Mitochondrial disorders of the nuclear genome.

Authors:  C Angelini; L Bello; M Spinazzi; C Ferrati
Journal:  Acta Myol       Date:  2009-07

6.  A perspective on neuronal cell death signaling and neurodegeneration.

Authors:  Scott Brady; Gerardo Morfini
Journal:  Mol Neurobiol       Date:  2010-05-18       Impact factor: 5.590

7.  Historical perspective on mitochondrial medicine.

Authors:  Salvatore DiMauro; Caterina Garone
Journal:  Dev Disabil Res Rev       Date:  2010

Review 8.  Emerging pathways for hereditary axonopathies.

Authors:  Stephan Züchner; Jeffery M Vance
Journal:  J Mol Med (Berl)       Date:  2005-08-31       Impact factor: 4.599

9.  Motor protein mutations cause a new form of hereditary spastic paraplegia.

Authors:  Andrés Caballero Oteyza; Esra Battaloğlu; Levent Ocek; Tobias Lindig; Jennifer Reichbauer; Adriana P Rebelo; Michael A Gonzalez; Yasar Zorlu; Burcak Ozes; Dagmar Timmann; Benjamin Bender; Günther Woehlke; Stephan Züchner; Ludger Schöls; Rebecca Schüle
Journal:  Neurology       Date:  2014-05-07       Impact factor: 9.910

10.  KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction.

Authors:  Jessica Duis; Shannon Dean; Carolyn Applegate; Amy Harper; Rui Xiao; Weimin He; James D Dollar; Lisa R Sun; Marta Biderman Waberski; Thomas O Crawford; Ada Hamosh; Carl E Stafstrom
Journal:  Ann Neurol       Date:  2016-08-24       Impact factor: 10.422

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