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Research 571–600 of 1000+
- The Functional Relevance of the Type 1 Cytokines IFN-γ and IL-2 in Alopecia Areata of C3H/HeJ Mice
- Rheumatoid arthritis and gouty arthritis in an adult patient with Down's syndrome
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Generalised Glucocorticoid Resistance
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- <i>Hoxc13</i> mutant mice lack external hair
- 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
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- 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?
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- 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