Literature DB >> 18842101

Drosophila models of neurodegenerative diseases.

Bingwei Lu1, Hannes Vogel.   

Abstract

Neurodegenerative diseases are progressive disorders of the nervous system that affect specific cellular populations in the central and peripheral nervous systems. Although most cases are sporadic, genes associated with familial cases have been identified, thus enabling the development of animal models. Invertebrates such as Drosophila have recently emerged as model systems for studying mechanisms of neurodegeneration in several major neurodegenerative diseases. These models are also excellent in vivo systems for the testing of therapeutic compounds. Genetic studies using these animal models have provided novel insights into the disease process. We anticipate that further exploration of the animal models will further our understanding of mechanisms of neurodegeneration as well as facilitate the development of rational treatments for debilitating degenerative diseases.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 18842101      PMCID: PMC3045805          DOI: 10.1146/annurev.pathol.3.121806.151529

Source DB:  PubMed          Journal:  Annu Rev Pathol        ISSN: 1553-4006            Impact factor:   23.472


  150 in total

1.  MARK, a novel family of protein kinases that phosphorylate microtubule-associated proteins and trigger microtubule disruption.

Authors:  G Drewes; A Ebneth; U Preuss; E M Mandelkow; E Mandelkow
Journal:  Cell       Date:  1997-04-18       Impact factor: 41.582

2.  Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.

Authors:  T Kitada; S Asakawa; N Hattori; H Matsumine; Y Yamamura; S Minoshima; M Yokochi; Y Mizuno; N Shimizu
Journal:  Nature       Date:  1998-04-09       Impact factor: 49.962

3.  Drosophila drop-dead mutations accelerate the time course of age-related markers.

Authors:  B Rogina; S Benzer; S L Helfand
Journal:  Proc Natl Acad Sci U S A       Date:  1997-06-10       Impact factor: 11.205

4.  The swiss cheese mutant causes glial hyperwrapping and brain degeneration in Drosophila.

Authors:  D Kretzschmar; G Hasan; S Sharma; M Heisenberg; S Benzer
Journal:  J Neurosci       Date:  1997-10-01       Impact factor: 6.167

5.  A preparation of Alzheimer paired helical filaments that displays distinct tau proteins by polyacrylamide gel electrophoresis.

Authors:  S G Greenberg; P Davies
Journal:  Proc Natl Acad Sci U S A       Date:  1990-08       Impact factor: 11.205

6.  Indices of oxidative stress and mitochondrial function in individuals with incidental Lewy body disease.

Authors:  D T Dexter; J Sian; S Rose; J G Hindmarsh; V M Mann; J M Cooper; F R Wells; S E Daniel; A J Lees; A H Schapira
Journal:  Ann Neurol       Date:  1994-01       Impact factor: 10.422

7.  par-1, a gene required for establishing polarity in C. elegans embryos, encodes a putative Ser/Thr kinase that is asymmetrically distributed.

Authors:  S Guo; K J Kemphues
Journal:  Cell       Date:  1995-05-19       Impact factor: 41.582

8.  Human amyloid precursor protein ameliorates behavioral deficit of flies deleted for Appl gene.

Authors:  L Luo; T Tully; K White
Journal:  Neuron       Date:  1992-10       Impact factor: 17.173

Review 9.  Neuropathological stageing of Alzheimer-related changes.

Authors:  H Braak; E Braak
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

10.  A68: a major subunit of paired helical filaments and derivatized forms of normal Tau.

Authors:  V M Lee; B J Balin; L Otvos; J Q Trojanowski
Journal:  Science       Date:  1991-02-08       Impact factor: 47.728

View more
  93 in total

Review 1.  Modeling human neurodegenerative diseases in transgenic systems.

Authors:  Miguel A Gama Sosa; Rita De Gasperi; Gregory A Elder
Journal:  Hum Genet       Date:  2011-12-14       Impact factor: 4.132

2.  In vivo reconstitution of gamma-secretase in Drosophila results in substrate specificity.

Authors:  Denise Stempfle; Ritu Kanwar; Alexander Loewer; Mark E Fortini; Gunter Merdes
Journal:  Mol Cell Biol       Date:  2010-04-26       Impact factor: 4.272

3.  Developmental expression of drop-dead is required for early adult survival and normal body mass in Drosophila melanogaster.

Authors:  Christine Lynn Sansone; Edward M Blumenthal
Journal:  Insect Biochem Mol Biol       Date:  2012-06-21       Impact factor: 4.714

Review 4.  Pharmacological lifespan extension of invertebrates.

Authors:  Mark Lucanic; Gordon J Lithgow; Silvestre Alavez
Journal:  Ageing Res Rev       Date:  2012-07-06       Impact factor: 10.895

Review 5.  Recent advances in using Drosophila to model neurodegenerative diseases.

Authors:  Bingwei Lu
Journal:  Apoptosis       Date:  2009-08       Impact factor: 4.677

6.  Signaling pathways involved in 1-octen-3-ol-mediated neurotoxicity in Drosophila melanogaster: implication in Parkinson’s disease.

Authors:  Arati A Inamdar; Prakash Masurekar; Muhammad Hossain; Jason R Richardson; Joan W Bennett
Journal:  Neurotox Res       Date:  2014-02       Impact factor: 3.911

7.  Environmental Presence of Hexavalent but Not Trivalent Chromium Causes Neurotoxicity in Exposed Drosophila melanogaster.

Authors:  Pallavi Singh; D Kar Chowdhuri
Journal:  Mol Neurobiol       Date:  2016-05-11       Impact factor: 5.590

8.  Exploring prion protein biology in flies: genetics and beyond.

Authors:  Diego E Rincon-Limas; Sergio Casas-Tinto; Pedro Fernandez-Funez
Journal:  Prion       Date:  2010-01-30       Impact factor: 3.931

Review 9.  Transgenic Drosophila models of Alzheimer's disease and tauopathies.

Authors:  Kanae Iijima-Ando; Koichi Iijima
Journal:  Brain Struct Funct       Date:  2009-12-05       Impact factor: 3.270

10.  Apolipoprotein E-mimetics inhibit neurodegeneration and restore cognitive functions in a transgenic Drosophila model of Alzheimer's disease.

Authors:  Svetlana Sarantseva; Svetlana Timoshenko; Olga Bolshakova; Eugenia Karaseva; Dmitry Rodin; Alexander L Schwarzman; Michael P Vitek
Journal:  PLoS One       Date:  2009-12-07       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.