Literature DB >> 33474528

Genetic interactions in a C. elegans sod-1 ALS model: glutamatergic neuron degeneration.

Jennifer F Osborne1,2, Katherine S Yanagi1,3,2, Anne C Hart1,2.   

Abstract

Entities:  

Year:  2021        PMID： 33474528      PMCID： PMC7812382          DOI： 10.17912/micropub.biology.000338

Source DB:  PubMed          Journal:  MicroPubl Biol        ISSN： 2578-9430


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  14 in total

1.  Mutant sensory cilia in the nematode Caenorhabditis elegans.

Authors:  L A Perkins; E M Hedgecock; J N Thomson; J G Culotti
Journal:  Dev Biol       Date:  1986-10       Impact factor: 3.582

2.  Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase.

Authors:  John Mitchell; Praveen Paul; Han-Jou Chen; Alex Morris; Miles Payling; Mario Falchi; James Habgood; Stefania Panoutsou; Sabine Winkler; Veronica Tisato; Amin Hajitou; Bradley Smith; Caroline Vance; Christopher Shaw; Nicholas D Mazarakis; Jacqueline de Belleroche
Journal:  Proc Natl Acad Sci U S A       Date:  2010-04-05       Impact factor: 11.205

3.  SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis.

Authors:  Faisal Fecto; Jianhua Yan; S Pavan Vemula; Erdong Liu; Yi Yang; Wenjie Chen; Jian Guo Zheng; Yong Shi; Nailah Siddique; Hasan Arrat; Sandra Donkervoort; Senda Ajroud-Driss; Robert L Sufit; Scott L Heller; Han-Xiang Deng; Teepu Siddique
Journal:  Arch Neurol       Date:  2011-11

4.  Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.

Authors:  D R Rosen; T Siddique; D Patterson; D A Figlewicz; P Sapp; A Hentati; D Donaldson; J Goto; J P O'Regan; H X Deng
Journal:  Nature       Date:  1993-03-04       Impact factor: 49.962

Review 5.  The role of tau (MAPT) in frontotemporal dementia and related tauopathies.

Authors:  R Rademakers; M Cruts; C van Broeckhoven
Journal:  Hum Mutat       Date:  2004-10       Impact factor: 4.878

6.  The genetics of Caenorhabditis elegans.

Authors:  S Brenner
Journal:  Genetics       Date:  1974-05       Impact factor: 4.562

Review 7.  Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis.

Authors:  Shuo-Chien Ling; Magdalini Polymenidou; Don W Cleveland
Journal:  Neuron       Date:  2013-08-07       Impact factor: 17.173

8.  Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.

Authors:  Han-Xiang Deng; Wenjie Chen; Seong-Tshool Hong; Kym M Boycott; George H Gorrie; Nailah Siddique; Yi Yang; Faisal Fecto; Yong Shi; Hong Zhai; Hujun Jiang; Makito Hirano; Evadnie Rampersaud; Gerard H Jansen; Sandra Donkervoort; Eileen H Bigio; Benjamin R Brooks; Kaouther Ajroud; Robert L Sufit; Jonathan L Haines; Enrico Mugnaini; Margaret A Pericak-Vance; Teepu Siddique
Journal:  Nature       Date:  2011-08-21       Impact factor: 49.962

9.  MAPT as a predisposing gene for sporadic amyotrophic lateral sclerosis in the Chinese Han population.

Authors:  Pu Fang; Wenyuan Xu; Chengsi Wu; Min Zhu; Xiaobing Li; Daojun Hong
Journal:  Neural Regen Res       Date:  2013-11-25       Impact factor: 5.135

10.  Single copy/knock-in models of ALS SOD1 in C. elegans suggest loss and gain of function have different contributions to cholinergic and glutamatergic neurodegeneration.

Authors:  Saba N Baskoylu; Jill Yersak; Patrick O'Hern; Sarah Grosser; Jonah Simon; Sarah Kim; Kelsey Schuch; Maria Dimitriadi; Katherine S Yanagi; Jeremy Lins; Anne C Hart
Journal:  PLoS Genet       Date:  2018-10-08       Impact factor: 5.917
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