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Xu Cao
Xu Cao
Peking University, UMich, UC Davis
Verified email at bjmu.edu.cn
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Year
Exome Sequencing Reveals Mutations in< i> TRPV3</i> as a Cause of Olmsted Syndrome
Z Lin, Q Chen, M Lee, X Cao, J Zhang, D Ma, L Chen, X Hu, H Wang, ...
The American Journal of Human Genetics 90 (3), 558-564, 2012
3432012
Selective disruption of high sensitivity heat activation but not capsaicin activation of TRPV1 channels by pore turret mutations
Y Cui, F Yang, X Cao, V Yarov-Yarovoy, KW Wang, J Zheng
The Journal of general physiology 139 (4), 273-283, 2012
1112012
Heteromeric heat-sensitive transient receptor potential channels exhibit distinct temperature and chemical response
W Cheng, F Yang, S Liu, CK Colton, C Wang, Y Cui, X Cao, MX Zhu, ...
Journal of Biological Chemistry 287 (10), 7279-7288, 2012
882012
Intracellular proton-mediated activation of TRPV3 channels accounts for the exfoliation effect of α-hydroxyl acids on keratinocytes
X Cao, F Yang, J Zheng, KW Wang
Journal of Biological Chemistry 287 (31), 25905-25916, 2012
742012
Divalent cations activate TRPV1 through promoting conformational change of the extracellular region
F Yang, L Ma, X Cao, KW Wang, J Zheng
Journal of General Physiology 143 (1), 91-103, 2014
642014
Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome
H Wang, X Cao, Z Lin, M Lee, X Jia, Y Ren, L Dai, L Guan, J Zhang, X Lin, ...
Human molecular genetics 24 (1), 243-250, 2015
602015
Divalent cations potentiate TRPV1 channel by lowering the heat activation threshold
X Cao, L Ma, F Yang, KW Wang, J Zheng
Journal of General Physiology 143 (1), 75-90, 2014
552014
The ER/PM microdomain, PI (4, 5) P2 and the regulation of STIM1–Orai1 channel function
X Cao, S Choi, JJ Maléth, S Park, M Ahuja, S Muallem
Cell calcium 58 (4), 342-348, 2015
542015
Mutation in AQP5, encoding aquaporin 5, causes palmoplantar keratoderma Bothnia type
X Cao, J Yin, H Wang, J Zhao, J Zhang, L Dai, J Zhang, H Jiang, Z Lin, ...
Journal of Investigative Dermatology 134, 284-287, 2014
492014
New and recurrent SERPINB7 mutations in seven Chinese patients with Nagashima-type palmoplantar keratosis
J Yin, G Xu, H Wang, J Zhao, L Duo, X Cao, Z Tang, Z Lin, Y Yang
The Journal of Investigative Dermatology 134 (8), 2269, 2014
472014
Crystal structure of the N-terminal ankyrin repeat domain of TRPV3 reveals unique conformation of finger 3 loop critical for channel function
DJ Shi, S Ye, X Cao, R Zhang, KW Wang
Protein & cell 4 (12), 942-950, 2013
452013
A TRPV4 channel C-terminal folding recognition domain critical for trafficking and function
L Lei, X Cao, F Yang, DJ Shi, YQ Tang, J Zheng, KW Wang
Journal of Biological Chemistry, 2013
432013
Gain-of-function mutations in TRPM4 activation gate cause progressive symmetric erythrokeratodermia
H Wang, Z Xu, BH Lee, S Vu, L Hu, M Lee, D Bu, X Cao, S Hwang, ...
Journal of Investigative Dermatology 139 (5), 1089-1097, 2019
412019
Activation of TRPV1 mediates thymic stromal lymphopoietin release via the Ca2+/NFAT pathway in airway epithelial cells
X Jia, H Zhang, X Cao, Y Yin, B Zhang
FEBS letters 588 (17), 3047-3054, 2014
352014
Visceral hyperalgesia induced by forebrain-specific suppression of native Kv7/KCNQ/M-current in mice
Y Bi, H Chen, J Su, X Cao, X Bian, KW Wang
Molecular pain 7, 1744-8069-7-84, 2011
292011
Genotype‒phenotype correlation of TRPV3-related Olmsted Syndrome
W Zhong, L Hu, X Cao, J Zhao, X Zhang, M Lee, H Wang, J Zhang, ...
Journal of Investigative Dermatology 141 (3), 545-554, 2021
232021
A novel degradation signal derived from distal C-terminal frameshift mutations of KCNQ2 protein which cause neonatal epilepsy
J Su, X Cao, KW Wang
Journal of Biological Chemistry 286 (50), 42949-42958, 2011
172011
Semidominant inheritance in olmsted syndrome
X Cao, H Wang, Y Li, M Lee, L Jiang, Y Zhou, C Feng, Z Lin, Y Yang
The Journal of investigative dermatology 136 (8), 1722-1725, 2016
142016
Exome sequencing reveals novel BCS1L mutations in siblings with hearing loss and hypotrichosis
J Zhang, L Duo, Z Lin, H Wang, J Yin, X Cao, J Zhao, L Dai, X Liu, ...
Gene 566 (1), 84-88, 2015
122015
A platform for assessing outer segment fate in primary human fetal RPE cultures
Q Zhang, F Presswalla, K Feathers, X Cao, BA Hughes, DN Zacks, ...
Experimental eye research 178, 212-222, 2019
102019
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