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Research 511–540 of 710
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- Comments concerning the real risk of sexual adverse events secondary to the use of 5-ARIs
- Vaccines, Infections, and Alopecia Areata
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- Cycle pilaire et alopécie X chez le chien
- Insulin Resistance and Polycystic Ovary Syndrome
- Molecular genetics of androgen insensitivity
- Reply
- Abstracts from the 2025 WDS Forum
- 원저 : 한국인 안드로겐 탈모증 환자에서 안드로겐 수용체의 CAG 반복 다형성에 관한 연구 -Preliminary Report-
- 13C-NMR study of 4-azasteroids in solution and solid state
- Case report: NUDT15 polymorphism and severe azathioprine-induced myelosuppression in a young Chinese female with systematic lupus erythematosus: a case analysis and literature review
- Simultaneous Typing of Erythrocyte Acid Phosphatase, Adenylate Kinase and Adenosine Deaminase in Human Hair Root Sheaths
- Pure Leydig cell tumor of the ovary: a rare presentation of a rare entity in a pregnant patient
- Gestational safety: No time for a pregnant pause
- Genetic analysis of the role of androgen metabolism in the pathogenesis of prostate cancer
- Minoxidil
- Forsythiasides: A review of the pharmacological effects
- Strange cutaneous abnormalities and polyposis in an Asiatic man
- Histomorphological study on the teat (mammary papilla) of Indian buffalo
- Caractérisation des Réactions Paradoxales Psoriasiformes Alopéciantes Induites par les Anti-TNFα chez des Patients Atteints de Maladies Inflammatoires Chroniques de l’Intestin
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Dynamic regulation of retinoic acid-binding proteins in developing, adult and neoplastic skin reveals roles for β-catenin and Notch signalling
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Hypogonadism as a Reversible Cause of Torsades de Pointes in Men
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Potassium Channel Openers Increase Aortic Elastic Fiber Formation and Reverse the Genetically Determined Elastin Deficit in the BN Rat
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Association between Alopecia Areata, Psoriasis Vulgaris, Thyroid Disease, and Metabolic Syndrome