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Research 301–330 of 1000+
- The vitamin D receptor, the skin and stem cells
- Genetic Hair Disorders: A Review
- Akt2 and SGK3 are both determinants of postnatal hair follicle development
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- Sustained Postnatal Skin Regeneration Upon Prenatal Application of Functionalized Collagen Scaffolds
- Niche work when you can get it: collagen XVII and the melanocyte stem cell
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Nelfb promotes dermal white adipose tissue formation through RNA Polymerase II mediated adipogenic gene regulation
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Lifestyle Diseases and the Hair Growth Cycle: A multidisciplinary approach using Nourkrin® with Marilex®, a proteoglycan replacement therapy, for anagen induction and maintenance
- Secondary Neoplasm Arising in Nevus Sebaceus of Jadassohn: A Case Report Emphasizing Early Recognition and Evaluation
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- Advances in dermatology research: A comprehensive literature review
- Early postnatal inhibition of neurosteroid synthesis changes the later-life adverse outcome of neonatal asphyxia in rats
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- BMP-FGF Signaling Axis Mediates Wnt-Induced Epidermal Stratification in Developing Mammalian Skin
- Mechanical forces in skin disorders
- Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
- EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- An Update of Congenital Adrenal Hyperplasia
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Acquired Progressive Kinking of Hair
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Caring for women with polycystic ovary syndrome