Literature DB >> 12849454

Mouse models for neurological disease.

Majid Hafezparast1, Azlina Ahmad-Annuar, Nicholas W Wood, Sarah J Tabrizi, Elizabeth M C Fisher.   

Abstract

The mouse has many advantages over human beings for the study of genetics, including the unique property that genetic manipulation can be routinely carried out in the mouse genome. Most importantly, mice and human beings share the same mammalian genes, have many similar biochemical pathways, and have the same diseases. In the minority of cases where these features do not apply, we can still often gain new insights into mouse and human biology. In addition to existing mouse models, several major programmes have been set up to generate new mouse models of disease. Alongside these efforts are new initiatives for the clinical, behavioural, and physiological testing of mice. Molecular genetics has had a major influence on our understanding of the causes of neurological disorders in human beings, and much of this has come from work in mice.

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Year:  2002        PMID: 12849454     DOI: 10.1016/s1474-4422(02)00100-x

Source DB:  PubMed          Journal:  Lancet Neurol        ISSN: 1474-4422            Impact factor:   44.182


  13 in total

Review 1.  Genetic Discoveries Drive Molecular Analyses and Targeted Therapeutic Options in the Epilepsies.

Authors:  Ryan S Dhindsa; David B Goldstein
Journal:  Curr Neurol Neurosci Rep       Date:  2015-10       Impact factor: 5.081

2.  Noninvasive, in vivo imaging of the mouse brain using photoacoustic microscopy.

Authors:  Erich W Stein; Konstantin Maslov; Lihong V Wang
Journal:  J Appl Phys       Date:  2009-05-19       Impact factor: 2.546

3.  Overexpression of NEUROG2 and NEUROG1 in human embryonic stem cells produces a network of excitatory and inhibitory neurons.

Authors:  Congyi Lu; Xi Shi; Andrew Allen; David Baez-Nieto; Alexandria Nikish; Neville E Sanjana; Jen Q Pan
Journal:  FASEB J       Date:  2019-01-30       Impact factor: 5.191

4.  Cln6 mutants associated with neuronal ceroid lipofuscinosis are degraded in a proteasome-dependent manner.

Authors:  Kristina Oresic; Britta Mueller; Domenico Tortorella
Journal:  Biosci Rep       Date:  2009-06       Impact factor: 3.840

5.  Expression profile and mitochondrial colocalization of Tdp1 in peripheral human tissues.

Authors:  Hok Khim Fam; Miraj K Chowdhury; Cheryl Walton; Kunho Choi; Cornelius F Boerkoel; Glenda Hendson
Journal:  J Mol Histol       Date:  2013-03-28       Impact factor: 2.611

6.  The legs at odd angles (Loa) mutation in cytoplasmic dynein ameliorates mitochondrial function in SOD1G93A mouse model for motor neuron disease.

Authors:  Ali Morsi El-Kadi; Virginie Bros-Facer; Wenhan Deng; Amelia Philpott; Eleanor Stoddart; Gareth Banks; Graham S Jackson; Elizabeth M C Fisher; Michael R Duchen; Linda Greensmith; Anthony L Moore; Majid Hafezparast
Journal:  J Biol Chem       Date:  2010-04-09       Impact factor: 5.157

7.  Noninvasive, in vivo imaging of blood-oxygenation dynamics within the mouse brain using photoacoustic microscopy.

Authors:  Erich W Stein; Konstantin Maslov; Lihong V Wang
Journal:  J Biomed Opt       Date:  2009 Mar-Apr       Impact factor: 3.170

8.  Sagittal Plane Kinematic Gait Analysis in C57BL/6 Mice Subjected to MOG35-55 Induced Experimental Autoimmune Encephalomyelitis.

Authors:  Maximillian Dj Fiander; Matthew Aj Chedrawe; Anna-Claire Lamport; Turgay Akay; George S Robertson
Journal:  J Vis Exp       Date:  2017-11-04       Impact factor: 1.355

Review 9.  Modeling neurological disorders using brain organoids.

Authors:  Daniel Y Zhang; Hongjun Song; Guo-Li Ming
Journal:  Semin Cell Dev Biol       Date:  2020-06-17       Impact factor: 7.727

10.  TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.

Authors:  Bradley J Turner; Dirk Bäumer; Nicholas J Parkinson; Jakub Scaber; Olaf Ansorge; Kevin Talbot
Journal:  BMC Neurosci       Date:  2008-10-28       Impact factor: 3.288

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