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Research 241–270 of 813
- Therapeutic inhibition of keratinocyte TRPV3 sensory channel by local anesthetic dyclonine
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Role of the Wnt signaling pathway in keratoacanthoma
- Acne and acneiform eruptions
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Trichodystrophies: A hair-raising differential diagnosis
- The Role of Histone Demethylases in Disease
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Electrophysiological and Histopathological Effects of Minoxidil on Penicillin-Induced Epilepsy Model in Rats
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Data from Synergistic Function of Smad4 and PTEN in Suppressing Forestomach Squamous Cell Carcinoma in the Mouse
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Genetic Defects of Female Sexual Differentiation
- 9. Immunology and Genetics
- Australasian Society for Dermatology Research Meeting, May 2007
- Syndromes of Severe Insulin Resistance (SSIRs)
- Insulin Resistance and Polycystic Ovary Syndrome
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- Pharmacological Activation of Thermo–Transient Receptor Potential Vanilloid 3 Channels Inhibits Hair Growth by Inducing Cell Death of Hair Follicle Outer Root Sheath
- Disease causing homozygous variants in the human hairless gene