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Research 30 of 371
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- TRPV3 as a Therapeutic Target for Itch
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- Influence of TRPV3 mutation on hair growth cycle in mice
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Structural mechanism of TRPV3 channel inhibition by the plant‐derived coumarin osthole
- Activation of TRPV3 Inhibits Lipogenesis and Stimulates Production of Inflammatory Mediators in Human Sebocytes—A Putative Contributor to Dry Skin Dermatoses
- Molecular determinants for the chemical activation of the warmth-sensitive TRPV3 channel by the natural monoterpenoid carvacrol
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Unlocking the therapeutic potential of TRPV3: Insights into thermosensation, channel modulation, and skin homeostasis involving TRPV3
- Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
- Different Ligands of the TRPV3 Cation Channel Cause Distinct Conformational Changes as Revealed by Intrinsic Tryptophan Fluorescence Quenching
- A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation
- Therapeutic inhibition of keratinocyte TRPV3 sensory channel by local anesthetic dyclonine
- TRPV3 Ion Channel: From Gene to Pharmacology
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Natural phenylethanoid glycoside forsythoside A alleviates androgenetic alopecia by selectively inhibiting TRPV3 channels in mice
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Molecular studies of transient receptor potential Vanilloid 3 (TRPV3)
- 738 Cryo-EM and molecular dynamics of TRPV3 channel in activated state reveal structural features implicated in severe itch and hyperkeratosis
- Activation of temperature-sensitive Ca2+-permeable TRPV3 channels by natural ï¡-hydroxyl acids causes exfoliation for skin-resurfacing
- 889 Trpv3 gain-of-function mutation impairs differentiation of hair follicle inner root sheath
- Structural Analyses of the Transient Receptor Potential Channels TRPV3 and TRPV6
- 1391 Immune cells may have a role in hair loss process caused by TRPV3 gain-of-function mutation
- Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome with Concomitant Lymphopenia: A Novel TP63 Mutation
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”