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Research 361–390 of 1000+
- The PDGF/PDGFR pathway as a drug target
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Genetic prediction of male pattern baldness
- Keratin disorders: from gene to therapy
- Interferon in the treatment of cutaneous T-cell lymphoma
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Wnt signaling in skin organogenesis
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Oral Manifestations of Hematologic and Nutritional Diseases
- Alopecia areata update
- Significance of the S100A4 Protein in Psoriasis
- Are sex discordant outcomes in COVID-19 related to sex hormones?
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Hair Restoration Surgery: The State of the Art
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- INTERFERONS IN DERMATOLOGY
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Congenital adrenal hyperplasia
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis