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Research 631–660 of 1000+
- Mesothelial Stem Cells and Stromal Vascular Fraction for Skin Rejuvenation
- The Function of Zinc in Animal, Plant, and Human Nutrition
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Androgenetic Alopecia
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Sexual dimorphism following in vitro ischemia in the response to neurosteroids and mechanisms of injury
- Androgens in SARS-CoV-2 Coronavirus Infections
- Serum 1, 25-dihydroxy vitamin D- vitamin D3- among obese Egyptian women with polycystic ovary syndrome
- Effects of non-contingent cocaine on 3alpha-androstanediol. I. Disruption of male sexual behavior
- Estrogen modulates mesenchymal-epidermal interactions in the adult nipple
- The role of pre-operative androgen stimulation in hypospadias surgery.
- Anti-proliferative effect of terpenes on human prostate cáncer cells: natural sources and their potential role as chemopreventive agents.
- Retardation of Preputial Wound Healing in Rats with Hypospadias Induced by Flutamide
- Characteristic Localization of Neuronatin in Rat Testis, Hair Follicle, Tongue, and Pancreas
- Debatable Topics in PCOS Patients
- Antioxidant enzyme expression of mRNA and protein in the epididymis of finasteride-treated male rat offspring during postnatal development
- To study the prevalence of cutaneous manifestationsin newborns and its correlation with defined maternal and neonatal factors
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Loose anagen hair syndrome in two patients with epidermolysis bullosa simplex, Dowling-Meara type
- Spontaneous hair hyperpigmentation in response to vitamin intake in pregnancy—A clue for homocystinuria
- Endocrine disruptors as risk factors for idiopathic premature thelarche in girls: A case-control study
- 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
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Androgens and Parkinson’s disease: the role in humans and in experiment
- Structure and Function of the Skin
- DERMATOLOGICAL AND SYSTEMIC REACTIONS TO HAIR DYES: CURRENT EVIDENCE AND MANAGEMENT
- Recent advances and challenges in 3D bioprinting for skin tissue regeneration
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- A Study of Trichoscopic Findings in Scalp Alopecias and Its Fruitfulness in A Tertiary Care Centre in India
- CASE REPORT: DERMATITIS IN A MIX DOG WITH TOPICAL CANDLENUT OIL THERAPY AND FINDING OF ANCYLOSTOMA SPP. INFECTION