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Research 30 of 440
- Influence of TRPV3 mutation on hair growth cycle in mice
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Hypotrichosis in a child with olmsted syndrome
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- News in brief
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- 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
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- TRPV3 Ion Channel: From Gene to Pharmacology
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Therapeutic inhibition of keratinocyte TRPV3 sensory channel by local anesthetic dyclonine
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- The Multifaceted Functions of TRPV4 and Calcium Oscillations in Tissue Repair
- Direct cellular reprogramming enables development of viral T antigen–driven Merkel cell carcinoma in mice
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Painful thickened skin on the soles of the feet
- 890 Development of pigmented reconstructed human epidermis model containing human melanoblasts from keratinocyte culture
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- Diagnostic approach to low‐renin hypertension
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Decay of Skin-Specific Gene Modules in Pangolins
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials