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Research 241–270 of 1000+
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Congenital adrenal hyperplasia
- Congenital atrichia and hypotrichosis
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- 5-Alpha-reductase deficiency in a Saudi "girl"
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Two females with hair loss
- Comparison of allogeneic stem cell transplant conditioning regimens in AML, MDS and CLL
- Genetic Defects of Female Sexual Differentiation
- Immunopathogenesis of Primary Cicatricial Alopecia
- Cutaneous Lupus Erythematosus
- Use of chemotherapy during human pregnancy
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Alopecia areata
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Morpho-Regulation of Ectodermal Organs
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Interferon in the treatment of cutaneous T-cell lymphoma
- The role of lymphocytes in the development and treatment of alopecia areata
- Influence of TRPV3 mutation on hair growth cycle in mice
- Sex Hormone-Binding Globulin (SHBG) as an Early Biomarker and Therapeutic Target in Polycystic Ovary Syndrome
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Oral Manifestations of Hematologic and Nutritional Diseases
- Alopecia areata update
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Genetic basis of polycystic ovary syndrome