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BK channel overexpression on plasma membrane of fibroblasts from Hutchinson-Gilford progeria syndrome

Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare genetic disorder wherein symptoms resembling aspects of aging are manifested at a very early age. It is a genetic condition that occurs due to a de novo mutation in the LMNA gene encoding for the nuclear structural protein lamin A. The...

詳細記述

保存先:
書誌詳細
出版年:Aging (Albany NY)
主要な著者: Zironi, Isabella, Gavoçi, Entelë, Lattanzi, Giovanna, Virelli, Angela, Amorini, Fabrizio, Remondini, Daniel, Castellani, Gastone
フォーマット: Artigo
言語:Inglês
出版事項: Impact Journals 2018
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6286842/
https://ncbi.nlm.nih.gov/pubmed/30398975
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/aging.101621
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