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Research 331–360 of 1000+
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Microneedles as the technique of drug delivery enhancement in diverse organs and tissues
- Melanocytes: The new Black
- A cross-specialty expert opinion on the management of hair loss in gynaecological and endocrinological disorders in Indian patients
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Nutritional management in women with polycystic ovary syndrome: A review study
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- Polycystic Ovary Syndrome: A Complex Interplay of Hormones and Metabolism
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Diagnostic approach to low‐renin hypertension
- Recent advances in the treatment of psoriasis
- Biology of Human Hair: Know Your Hair to Control It
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- The Clinical Presentation of Systemic Lupus Erythematosus
- 1379 Cell of origin contributes to the melanoma diversity
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Review on Diagnostic and Managerial Consequences of PCOS Among Females
- The Role of Hormonal Imbalances in Amenorrhea
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Role of skin enzymes in metabolism of topical drugs