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Research 121–150 of 1000+
- Learning from nudity: lessons from the nude phenotype
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- The role of dutasteride in the treatment of benign prostatic obstruction and related conditions
- Plant cell culture as emerging technology for production of active cosmetic ingredients
- Adverse health effects of androgen use
- Epidermal growth factor, innovation and safety
- The crosstalk of monocyte-neutrophil in hair follicles regulates neutrophil transepidermal migration in contact dermatitis
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Beyond Expectations
- Dermatoscopy of hair shaft disorders
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Congenital hair loss disorders: Rare, but not too rare
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Progeroide Syndrome
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- The urine as a diagnostic key for a homozygous EGFR mutation
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Stem Cells and their Niches
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders