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Research 391–420 of 1000+
- Congenital adrenal hyperplasia
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men
- Male androgenetic alopecia (Part II)
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Investigating the Safety and Efficacy of Platelet-Rich Plasma (PRP) Treatment for Female Androgenetic Alopecia: Review of the Literature
- 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
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia
- Function of KLF4 in Stem Cell Biology
- Ectodysplasin-A2 induces dickkopf 1 expression in human balding dermal papilla cells overexpressing the ectodysplasin A2 receptor
- Markers of peripheral androgen action in vivo and in vitro
- Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis
- How a Bird Gets Its Feathers: Insights from Chromatin Looping
- Biotechs target stagnant baldness market
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Increased expression of psoriasin (S100A7) and interleukin 17 (IL-17) in lesional skin in lichen planopilaris
- Design and development of cosmeceutical cream for hyperpigmentation and anti-aging
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- 5-Alpha-reductase deficiency in a Saudi "girl"
- Combined activity of selenite-resistant bacteria and Pisum sativum sprout extract against Malassezia furfur: A preliminary qualitative evaluation
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy