Literature DB >> 16240358

DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.

Grazia Annesi1, Giovanni Savettieri, Pierfrancesco Pugliese, Marco D'Amelio, Patrizia Tarantino, Paolo Ragonese, Vincenzo La Bella, Tommaso Piccoli, Donatella Civitelli, Ferdinanda Annesi, Brigida Fierro, Federico Piccoli, Gennarina Arabia, Manuela Caracciolo, Innocenza Claudia Cirò Candiano, Aldo Quattrone.   

Abstract

DJ-1 gene mutations have been found to cause early-onset Parkinson's disease. We report a family from southern Italy with three brothers affected by early-onset parkinsonism, dementia, and amyotrophic lateral sclerosis. Molecular analysis of the DJ-1 gene in two living patients showed a novel homozygous mutation in exon 7 (E163K) and a new homozygous mutation (g.168_185dup) in the promoter region of the gene. Both mutations cosegregated with the disease and were detected in a heterozygous state in the patients' mother and their healthy siblings. Our findings expand the spectrum of clinical presentations associated with mutations in DJ-1 gene.

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Year:  2005        PMID: 16240358     DOI: 10.1002/ana.20666

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


  61 in total

Review 1.  The role of cysteine oxidation in DJ-1 function and dysfunction.

Authors:  Mark A Wilson
Journal:  Antioxid Redox Signal       Date:  2011-01-14       Impact factor: 8.401

2.  Engineered disulfide bonds restore chaperone-like function of DJ-1 mutants linked to familial Parkinson's disease.

Authors:  Todd Logan; Lindsay Clark; Soumya S Ray
Journal:  Biochemistry       Date:  2010-07-13       Impact factor: 3.162

3.  The MMACHC proteome: hallmarks of functional cobalamin deficiency in humans.

Authors:  Luciana Hannibal; Patricia M DiBello; Michelle Yu; Abby Miller; Sihe Wang; Belinda Willard; David S Rosenblatt; Donald W Jacobsen
Journal:  Mol Genet Metab       Date:  2011-03-24       Impact factor: 4.797

4.  Structural effects of Parkinson's disease linked DJ-1 mutations.

Authors:  Gaetano Malgieri; David Eliezer
Journal:  Protein Sci       Date:  2008-05       Impact factor: 6.725

Review 5.  DJ-1, PINK1, and their effects on mitochondrial pathways.

Authors:  Mark R Cookson
Journal:  Mov Disord       Date:  2010       Impact factor: 10.338

Review 6.  The phenotypic variability of amyotrophic lateral sclerosis.

Authors:  Bart Swinnen; Wim Robberecht
Journal:  Nat Rev Neurol       Date:  2014-10-14       Impact factor: 42.937

7.  Genetic Counseling Dilemmas for a Patient with Sporadic Amyotrophic Lateral Sclerosis, Frontotemporal Degeneration & Parkinson's Disease.

Authors:  Vittorio Mantero; Claudia Tarlarini; Angelo Aliprandi; Giuseppe Lauria; Andrea Rigamonti; Lucia Abate; Paola Origone; Paola Mandich; Silvana Penco; Andrea Salmaggi
Journal:  J Genet Couns       Date:  2017-03-01       Impact factor: 2.537

8.  DJ-1 deficient mice demonstrate similar vulnerability to pathogenic Ala53Thr human alpha-syn toxicity.

Authors:  Chenere P Ramsey; Elpida Tsika; Harry Ischiropoulos; Benoit I Giasson
Journal:  Hum Mol Genet       Date:  2010-01-20       Impact factor: 6.150

9.  The E163K DJ-1 mutant shows specific antioxidant deficiency.

Authors:  Chenere P Ramsey; Benoit I Giasson
Journal:  Brain Res       Date:  2008-09-16       Impact factor: 3.252

10.  Identification of a novel functional deletion variant in the 5'-UTR of the DJ-1 gene.

Authors:  Rowena J Keyser; Lize van der Merwe; Mauritz Venter; Craig Kinnear; Louise Warnich; Jonathan Carr; Soraya Bardien
Journal:  BMC Med Genet       Date:  2009-10-13       Impact factor: 2.103

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