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Research 241–270 of 1000+
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Hair Follicle Immune Privilege Revisited: The Key to Alopecia Areata Management
- The Okuda Papers: an extraordinary - but unfortunately unrecognized - piece of work that could have changed the history of hair transplantation
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- 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
- Learning from nudity: lessons from the nude phenotype
- The character “hairless” in the mouse
- A Clinical Approach to Severe Insulin Resistance
- Skin manifestations among<i>GATA2</i>-deficient patients
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Cyclosporine-Induced Alopecia in Childhood Nephrotic Syndrome – A Case Report
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Testosterone and dihydrotestosterone production in genetically furless and furred male rabbits and effects on growth.
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- The Editor's Choice
- Oral Presentations
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Identification of the cell lineage at the origin of basal cell carcinoma
- Finasteride-induced gynecomastia