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Research 481–510 of 1000+
- 0980 Tanshinone capsule enhances hair follicle regeneration in a mouse model of androgenetic alopecia via IGF1 and Wnt/β-catenin pathway
- Exploring the Complexities of TGF-beta Signaling in Keloids: Beyond the Classical Smad Pathway
- Insulin-like Growth Factor 1 (IGF-1) in Hair Regeneration: Mechanistic Pathways and Therapeutic Potential
- Fgf21 Deficiency Delays Hair Follicle Cycling and Modulates miRNA–Target Gene Interactions in Mice
- Mechanotransduction unifies healthy non-diabetic wound healing over time by promoting a Cd14+/C1qa+ fibroblast subpopulation
- Gene Expression Profiles of Melanocytes Over-Expressing miR-5110 in Alpaca
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Australasian Society for Dermatology Research Meeting, May 2006
- Single-cell chromatin landscapes of mouse skin development
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Light-Emitting Hair Follicles: Studying Skin Regeneration With In Vivo Imaging
- Congenital atrichia and hypotrichosis
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Congenital adrenal hyperplasia
- Biotinidase deficiency characterized by skin and hair findings
- Woolly Antics between the Sheaths
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Role of skin enzymes in metabolism of topical drugs
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner