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The Cellular and Physiological Functions of the Lowe Syndrome Protein OCRL1

Phosphoinositide lipids play a key role in cellular physiology, participating in a wide array of cellular processes. Consequently, mutation of phosphoinositide-metabolizing enzymes is responsible for a growing number of diseases in humans. Two related disorders, oculocerebrorenal syndrome of Lowe (O...

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Bibliografski detalji
Izdano u:Traffic
Glavni autori: Mehta, Zenobia B, Pietka, Grzegorz, Lowe, Martin
Format: Artigo
Jezik:Inglês
Izdano: John Wiley & Sons A/S 2014
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4278560/
https://ncbi.nlm.nih.gov/pubmed/24499450
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/tra.12160
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