A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome.
Human monogenic pain syndromes have provided important insights into the molecular mechanisms that underlie normal and pathological pain states. We describe an autosomal-dominant familial episodic pain syndrome characterized by episodes of debilitating upper body pain, triggered by fasting and physi...
Main Authors: | Kremeyer, B, Lopera, F, Cox, J, Momin, A, Rugiero, F, Marsh, S, Woods, C, Jones, N, Paterson, K, Fricker, F, Villegas, A, Acosta, N, Pineda-Trujillo, N, Ramírez, J, Zea, J, Burley, M, Bedoya, G, Bennett, D, Wood, J, Ruiz-Linares, A |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2010
|
Similar Items
-
TRPA1 as Target in Myocardial Infarction
by: Clara Hoebart, et al.
Published: (2023-01-01) -
Caco-2 Intestinal Permeability Study of Phenyltetrahydroquinolinedione Derivative – TRPA₁ Antagonist
by: N. V. Pyatigorskaya, et al.
Published: (2022-09-01) -
The Agonist Action of Alkylphenols on TRPA1 Relates to Their Effects on Membrane Lipid Order: Implications for TRPA1-Mediated Chemosensation
by: Justyna B. Startek, et al.
Published: (2021-03-01) -
Effects of TRPA1 activation and inhibition on TRPA1 and CGRP expression in dorsal root ganglion neurons
by: Xiao-Lei Wang, et al.
Published: (2019-01-01) -
The role of TRPA1 channels in thermosensation
by: Hao Zhang, et al.
Published: (2022-12-01)