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Research 31–60 of 1000+
- Gender differences in skin: A review of the literature
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Standards of Care for the Health of Transsexual, Transgender, and Gender-Nonconforming People, Version 7
- Genetic Defects of Female Sexual Differentiation
- THE PATHOGENESIS OF ALOPECIA AREATA
- Endocrine Treatment of Transsexual Persons:An Endocrine Society Clinical Practice Guideline
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Testosterone, sex hormone-binding globulin and dehydroepiandrosterone levels and cervical length of Egyptian women with a history of recurrent miscarriages, polycystic ovary syndrome and without the conditions at three stages of pregnancy
- Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
- Immuno-Endocrinology of COVID-19: The Key Role of Sex Hormones
- Kelulut Honey Regulates Sex Steroid Receptors in a Polycystic Ovary Syndrome Rat Model
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- Testosterone: The Male Sex Hormone
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- The Impact of Sulforaphane on Sex-Specific Conditions and Hormone Balance: A Comprehensive Review
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Current understanding and treatment of sex hormone-related hair diseases
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- The Role of Hormonal Imbalances in Amenorrhea
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients