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Research 841–870 of 1000+
- Congenital atrichia and hypotrichosis
- Biotinidase deficiency characterized by skin and hair findings
- Effect of 5α-Dihydrotestosterone and Testosterone on Apoptosis in Human Dermal Papilla Cells
- The Clinical Presentation of Systemic Lupus Erythematosus
- Congenital adrenal hyperplasia
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Traditional and Integrative Approaches to the Treatment of Alopecia
- Diagnostic approach to low‐renin hypertension
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Androgens Affect the Activity of Human Sebocytes in Culture in a Manner Dependent on the Localization of the Sebaceous Glands and Their Effect Is Antagonized by Spironolactone
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Transcriptomic inspection revealed a possible pathway regulating the formation of the high-quality brush hair in Chinese Haimen goat ( <i>Capra hircus</i> )
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Jojoba (Simmondsia chinensis (Link) Schneider): An important Medicinal Plant- The Gold of the Desert
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Hashimoto Thyroiditis - A Comprehensive Review
- Immunopathogenesis of Primary Cicatricial Alopecia
- Nonclassic adrenal hyperplasia
- Association between genetically predicted rheumatoid arthritis and alopecia areata: a two-sample Mendelian randomization study
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Acquired Alopecias in Mexican Adults: A Clinical and Epidemiological Study of 1,888 Patients
- Nevus Sebaceus With Novel HRAS Sequence Variant Mutation Misdiagnosed as Alopecia Areata
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- The crosstalk of monocyte-neutrophil in hair follicles regulates neutrophil transepidermal migration in contact dermatitis