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Literature DB >> 18986339

TDP-43 neuropathology is similar in sporadic amyotrophic lateral sclerosis with or without TDP-43 mutations.

R Pamphlett, N Luquin, C McLean, S Kum Jew, L Adams.

Abstract

Entities: Disease Gene

Mesh：

Substances：
DNA-Binding Proteins

Year: 2009 PMID： 18986339 DOI： 10.1111/j.1365-2990.2008.00982.x

Source DB: PubMed Journal: Neuropathol Appl Neurobiol ISSN： 0305-1846 Impact factor: 8.090

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Cited

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20 in total

Review 1. Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration.

Authors: Edward B Lee; Virginia M-Y Lee; John Q Trojanowski
Journal: Nat Rev Neurosci Date: 2011-11-30 Impact factor: 34.870

2. Cutaneous somatic and autonomic nerve TDP-43 deposition in amyotrophic lateral sclerosis.

Authors: Yuting Ren; Wenxiu Liu; Yifan Li; Bo Sun; Yanran Li; Fei Yang; Hongfen Wang; Mao Li; Fang Cui; Xusheng Huang
Journal: J Neurol Date: 2018-05-26 Impact factor: 4.849

3. Wild-type and A315T mutant TDP-43 exert differential neurotoxicity in a Drosophila model of ALS.

Authors: Patricia S Estes; Ashley Boehringer; Rebecca Zwick; Jonathan E Tang; Brianna Grigsby; Daniela C Zarnescu
Journal: Hum Mol Genet Date: 2011-03-26 Impact factor: 6.150

Review 4. Modeling ALS and FTLD proteinopathies in yeast: an efficient approach for studying protein aggregation and toxicity.

Authors: Dmitry Kryndushkin; Frank Shewmaker
Journal: Prion Date: 2011-10-01 Impact factor: 3.931

5. Partial loss of TDP-43 function causes phenotypes of amyotrophic lateral sclerosis.

Authors: Chunxing Yang; Hongyan Wang; Tao Qiao; Bin Yang; Leonardo Aliaga; Linghua Qiu; Weijia Tan; Johnny Salameh; Diane M McKenna-Yasek; Thomas Smith; Lingtao Peng; Melissa J Moore; Robert H Brown; Huaibin Cai; Zuoshang Xu
Journal: Proc Natl Acad Sci U S A Date: 2014-03-10 Impact factor: 11.205

TDP-43 neuropathology is similar in sporadic amyotrophic lateral sclerosis with or without TDP-43 mutations.

Review 1. Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration.

2. Cutaneous somatic and autonomic nerve TDP-43 deposition in amyotrophic lateral sclerosis.

3. Wild-type and A315T mutant TDP-43 exert differential neurotoxicity in a Drosophila model of ALS.

Review 4. Modeling ALS and FTLD proteinopathies in yeast: an efficient approach for studying protein aggregation and toxicity.

5. Partial loss of TDP-43 function causes phenotypes of amyotrophic lateral sclerosis.

6. CGG repeats in RNA modulate expression of TDP-43 in mouse and fly models of fragile X tremor ataxia syndrome.

Review 7. TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration.

8. Disease-associated mutations of TDP-43 promote turnover of the protein through the proteasomal pathway.

Review 9. Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis.

Review 10. Molecular neuropathology of TDP-43 proteinopathies.