Gain-of-Function Mutations in TRPM4 Activation Gate Cause Progressive Symmetric Erythrokeratodermia-Reference-Cited by-同舟云学术

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Gain-of-Function Mutations in TRPM4 Activation Gate Cause Progressive Symmetric Erythrokeratodermia

Published:2019-05 Issue:5 Volume:139 Page:1089-1097
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Wang Huijun,Xu Zhe,Lee Bo Hyun,Vu Simon,Hu Linghan,Lee Mingyang,Bu Dingfang,Cao Xu,Hwang Samuel,Yang Yong,Zheng Jie,Lin Zhimiao

Funder

National Natural Science Foundation of China

China National Funds for Distinguished Young Scientists

China National Funds for Excellent Young Scientists

National Institutes of Health Funds

Health and Family Planning Research and Development Foundation of Shunyi District

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference38 articles.

1. TRPM4 enhances cell proliferation through up-regulation of the β-catenin signaling pathway;Armisen;J Cell Physiol,2011

2. Structure of the human TRPM4 ion channel in a lipid nanodisc;Autzen;Science,2018

3. Epidermal TRPM8 channel isoform controls the balance between keratinocyte proliferation and differentiation in a cold-dependent manner;Bidaux;Proc Natl Acad Sci USA,2015

4. Epidermal homeostasis: a balancing act of stem cells in the skin;Blanpain;Nat Rev Mol Cell Biol,2009

5. Defective channels lead to an impaired skin barrier;Blaydon;J Cell Sci,2014

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