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Research 721–750 of 1000+
- Alopecia areata update
- Oxidative Activity of the Type 2 Isozyme of 17β-Hydroxysteroid Dehydrogenase (17β-HSD) Predominates in Human Sebaceous Glands
- Are sex discordant outcomes in COVID-19 related to sex hormones?
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Hair Restoration Surgery: The State of the Art
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- LncRNAs in Secondary Hair Follicle of Cashmere Goat: Identification, Expression, and Their Regulatory Network in Wnt Signaling Pathway
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- <i>Pten</i> loss in Lgr5<sup>+</sup> hair follicle stem cells promotes SCC development
- Review of Human Hair Follicle Biology: Dynamics of Niches and Stem Cell Regulation for Possible Therapeutic Hair Stimulation for Plastic Surgeons
- Identification of ultraviolet B radiation-induced microRNAs in normal human dermal papilla cells
- PERICARDIAL EFFUSIONS ASSOCIATED WITH MINOXIDIL
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Protein kinase C is a key target for attenuation of Leigh syndrome by rapamycin
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis
- Hair, Hormones, and High-Risk Prostate Cancer
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Combined activity of selenite-resistant bacteria and Pisum sativum sprout extract against Malassezia furfur: A preliminary qualitative evaluation
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Ultraviolet-Enhanced Trichoscopy—A New Tool to Assess Pili Annulati
- Evaluation of Eclipta alba L. selections for higher biomass and bioactive compound