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Research 421–450 of 1000+
- Topical Finasteride: A Comprehensive Review of Androgenetic Alopecia Management for Men and Women
- Brown adipose tissue in the form of innovative approach for polycystic ovary syndrome treatmentstill long time to reach clinical arena: a narrative review
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Endocrinology
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Hidradenitis suppurativa: A practical review of possible medical treatments based on over 350 hidradenitis patients
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- Current Advanced Therapies Based on Human Mesenchymal Stem Cells for Skin Diseases
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Recently Identified Forms of Epidermolysis Bullosa
- Biomaterial-based mechanical regulation facilitates scarless wound healing with functional skin appendage regeneration
- Ichthyosis with confetti: clinics, molecular genetics and management
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Inflammatory perspectives of polycystic ovary syndrome: role of specific mediators and markers
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Normal Pubertal Development in Daughters of Women With PCOS: A Controlled Study
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Genetic Hair Disorders: A Review
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Wanted, dead and alive: Why a multidisciplinary approach is needed to unlock hair treatment potential
- Developmental genetics of color pattern establishment in cats
- Novel insights into the pathways regulating the canine hair cycle and their deregulation in alopecia X