KATP Channel Expression and Genetic Polymorphisms Associated with Progression and Survival in Amyotrophic Lateral Sclerosis-Reference-Cited by-同舟云学术

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KATP Channel Expression and Genetic Polymorphisms Associated with Progression and Survival in Amyotrophic Lateral Sclerosis

Published:2018-02-28 Issue:10 Volume:55 Page:7962-7972
ISSN:0893-7648
Container-title:Molecular Neurobiology
language:en
Short-container-title:Mol Neurobiol

Author:

Vidal-Taboada José M.^ORCID,Pugliese Marco^ORCID,Salvadó Maria^ORCID,Gámez Josep^ORCID,Mahy Nicole^ORCID,Rodríguez Manuel J.^ORCID

Funder

Agència de Gestió d’Ajuts Universitaris i de Recerca

Comissió Interdepartamental de Recerca i Innovació Tecnològica

Ministerio de Sanidad, Servicios Sociales e Igualdad

Secretaría de Estado de Investigación, Desarrollo e Innovación

Publisher

Springer Science and Business Media LLC

Subject

Neuroscience (miscellaneous),Cellular and Molecular Neuroscience,Neurology

Link

http://link.springer.com/article/10.1007/s12035-018-0970-7/fulltext.html

Reference63 articles.

1. Conte A, Lattante S, Luigetti M, del Grande A, Romano A, Marcaccio A, Marangi G, Rossini PM et al (2012) Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation. J Neurol Neurosurg Psychiatry 83:1201–1203. https://doi.org/10.1136/jnnp-2012-302897

2. Kiernan MC, Vucic S, Cheah BC, Turner M, Eisen A, Hardiman O et al (2011) Amyotrophic lateral sclerosis. Lancet 377:942–955. https://doi.org/10.1016/S0140-6736(10)61156-7

3. Rowland LP, Shneider NA (2001) Amyotrophic lateral sclerosis. N Engl J Med 344:1688–1700. https://doi.org/10.1056/NEJM200105313442207

4. Swinnen B, Robberecht W (2014) The phenotypic variability of amyotrophic lateral sclerosis. Nat Rev Neurol 10:661–670. https://doi.org/10.1038/nrneurol.2014.184

5. Mackenzie I, Rademakers R, Neumann M (2010) TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia. Lancet Neurol 9:995–1007. https://doi.org/10.1016/S1474-4422(10)70195-2

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1. Genetic factors for survival in amyotrophic lateral sclerosis: an integrated approach combining a systematic review, pairwise and network meta-analysis;BMC Medicine;2022-06-27

2. A chemogenomic approach is required for effective treatment of amyotrophic lateral sclerosis;Clinical and Translational Medicine;2022-01

3. ATP-binding cassette transporters and neurodegenerative diseases;Essays in Biochemistry;2021-12

4. Genetic Variants of Potassium Voltage-gated Channel Subfamily J Member 11 in Gestational Diabetes Mellitus: A Case-control Study;Maternal-Fetal Medicine;2019-12-20

5. ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9;Nature Communications;2019-10-01

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