Gain of function of TMEM16E/ANO5 scrambling activity caused by a mutation associated with gnathodiaphyseal dysplasia

Overview of attention for article published in Cellular and Molecular Life Sciences, November 2017

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RT @BiofisicaCnr: @BiofisicaCnr studies mutations in human TMEM16E/ANO5 gene 🧬connected to gnathodiaphyseal dysplasia (GDD), a rare bone ma…

@BiofisicaCnr studies mutations in human TMEM16E/ANO5 gene 🧬connected to gnathodiaphyseal dysplasia (GDD), a rare bone malformation and fragility disorder, and two types of muscular dystrophy (MD). https://t.co/Ke8Xv4LkHo https://t.co/bk6YHmvTrs #RareDisea

Gain of function of TMEM16E/ANO5 scrambling activity caused by mutation assoc. with #gnathodiaphyseal dysplasia https://t.co/OfgiOeiDrj

Still the enigmatic TMEM16 channel family. https://t.co/2aOly3I2x0

Demonstrated #lipid scrambling activity of TMEM16E/ANO5 #protein and gain of function caused by a #mutation causing gnathodiaphyseal #dysplasia #ResearchHighlight in Cellular and Molecular Life Sciences @SpringerNature #physiology #bonedisease #scramblase