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Research 661–690 of 807
- 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
- The roles of Wnt/β‐catenin pathway in tissue development and regenerative medicine
- Learning from nudity: lessons from the nude phenotype
- Safety of testosterone treatment in postmenopausal women
- What causes hidradenitis suppurativa ?—15 years after
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Nutrition Strategy and Life Style in Polycystic Ovary Syndrome—Narrative Review
- 5-Alpha reductase deficiency
- Monilethrix Treated with Minoxidil
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Alopecia in Epidermolysis Bullosa
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Pharmacological Activation of Thermo–Transient Receptor Potential Vanilloid 3 Channels Inhibits Hair Growth by Inducing Cell Death of Hair Follicle Outer Root Sheath
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Synchronizing actin and microtubules for axonal branching
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Trichodystrophies: A hair-raising differential diagnosis
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Congenital Atrichia: A Case Report
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- Hair Growth Defects of Diabetic and Hypercholesterolemic Wistar Albino Rats and Amelioration of Fish Oil-Treatment
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Watching hair grow
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders