Literature DB >> 29128849

Genetic strategies to tackle neurological diseases in fruit flies.

Mümine Şentürk1, Hugo J Bellen2.   

Abstract

Drosophila melanogaster is a genetic model organism that has contributed to the discovery of numerous genes whose human homologues are associated with diseases. The development of sophisticated genetic tools to manipulate its genome accelerates the discovery of the genetic basis of undiagnosed human diseases and the elucidation of molecular pathogenic events of known and novel diseases. Here, we discuss various approaches used in flies to assess the function of the fly homologues of disease-associated genes. We highlight how systematic and combinatorial approaches based on recently established methods provide us with integrated tool sets that can be applied to the study of neurodevelopmental and neurodegenerative disorders.
Copyright © 2017 Elsevier Ltd. All rights reserved.

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Year:  2017        PMID: 29128849      PMCID: PMC5940587          DOI: 10.1016/j.conb.2017.10.017

Source DB:  PubMed          Journal:  Curr Opin Neurobiol        ISSN: 0959-4388            Impact factor:   6.627


  70 in total

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Journal:  Genetics       Date:  2010-09-27       Impact factor: 4.562

3.  MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.

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Journal:  Am J Hum Genet       Date:  2017-05-11       Impact factor: 11.025

4.  Fruit flies in biomedical research.

Authors:  Michael F Wangler; Shinya Yamamoto; Hugo J Bellen
Journal:  Genetics       Date:  2015-01-26       Impact factor: 4.562

5.  Transcellular spreading of huntingtin aggregates in the Drosophila brain.

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Review 6.  Drosophila as an In Vivo Model for Human Neurodegenerative Disease.

Authors:  Leeanne McGurk; Amit Berson; Nancy M Bonini
Journal:  Genetics       Date:  2015-10       Impact factor: 4.562

7.  The Q system: a repressible binary system for transgene expression, lineage tracing, and mosaic analysis.

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9.  Nitric oxide mediates glial-induced neurodegeneration in Alexander disease.

Authors:  Liqun Wang; Tracy L Hagemann; Hermann Kalwa; Thomas Michel; Albee Messing; Mel B Feany
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Authors:  Koen J T Venken; Joseph W Carlson; Karen L Schulze; Hongling Pan; Yuchun He; Rebecca Spokony; Kenneth H Wan; Maxim Koriabine; Pieter J de Jong; Kevin P White; Hugo J Bellen; Roger A Hoskins
Journal:  Nat Methods       Date:  2009-06       Impact factor: 28.547

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  19 in total

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Journal:  Hum Mol Genet       Date:  2020-06-03       Impact factor: 6.150

2.  De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia.

Authors:  Oguz Kanca; Jonathan C Andrews; Pei-Tseng Lee; Chirag Patel; Stephen R Braddock; Anne M Slavotinek; Julie S Cohen; Cynthia S Gubbels; Kimberly A Aldinger; Judy Williams; Maanasa Indaram; Ali Fatemi; Timothy W Yu; Pankaj B Agrawal; Gilbert Vezina; Cas Simons; Joanna Crawford; C Christopher Lau; Wendy K Chung; Thomas C Markello; William B Dobyns; David R Adams; William A Gahl; Michael F Wangler; Shinya Yamamoto; Hugo J Bellen; May Christine V Malicdan
Journal:  Am J Hum Genet       Date:  2019-07-18       Impact factor: 11.025

Review 3.  The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.

Authors:  A Jeremy Willsey; Montana T Morris; Sheng Wang; Helen R Willsey; Nawei Sun; Nia Teerikorpi; Tierney B Baum; Gerard Cagney; Kevin J Bender; Tejal A Desai; Deepak Srivastava; Graeme W Davis; Jennifer Doudna; Edward Chang; Vikaas Sohal; Daniel H Lowenstein; Hao Li; David Agard; Michael J Keiser; Brian Shoichet; Mark von Zastrow; Lennart Mucke; Steven Finkbeiner; Li Gan; Nenad Sestan; Michael E Ward; Ruth Huttenhain; Tomasz J Nowakowski; Hugo J Bellen; Loren M Frank; Mustafa K Khokha; Richard P Lifton; Martin Kampmann; Trey Ideker; Matthew W State; Nevan J Krogan
Journal:  Cell       Date:  2018-07-26       Impact factor: 41.582

4.  The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder.

Authors:  Scott Barish; Mumine Senturk; Kelly Schoch; Amanda L Minogue; Diego Lopergolo; Chiara Fallerini; Jake Harland; Jacob H Seemann; Nicholas Stong; Peter G Kranz; Sujay Kansagra; Mohamad A Mikati; Joan Jasien; Mays El-Dairi; Paolo Galluzzi; Francesca Ariani; Alessandra Renieri; Francesca Mari; Michael F Wangler; Swathi Arur; Yong-Hui Jiang; Shinya Yamamoto; Vandana Shashi; Hugo J Bellen
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Review 5.  Fly for ALS: Drosophila modeling on the route to amyotrophic lateral sclerosis modifiers.

Authors:  Francesco Liguori; Susanna Amadio; Cinzia Volonté
Journal:  Cell Mol Life Sci       Date:  2021-07-28       Impact factor: 9.261

6.  The fruit fly at the interface of diagnosis and pathogenic mechanisms of rare and common human diseases.

Authors:  Hugo J Bellen; Michael F Wangler; Shinya Yamamoto
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7.  An expanded toolkit for gene tagging based on MiMIC and scarless CRISPR tagging in Drosophila.

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Review 8.  Unraveling Novel Mechanisms of Neurodegeneration Through a Large-Scale Forward Genetic Screen in Drosophila.

Authors:  Samantha L Deal; Shinya Yamamoto
Journal:  Front Genet       Date:  2019-01-14       Impact factor: 4.599

Review 9.  Insights into C9ORF72-Related ALS/FTD from Drosophila and iPSC Models.

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Review 10.  Recent Developments in Using Drosophila as a Model for Human Genetic Disease.

Authors:  Christine Oriel; Paul Lasko
Journal:  Int J Mol Sci       Date:  2018-07-13       Impact factor: 5.923

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