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Research 541–570 of 1000+
- Effect of conditioned media collected from human amniotic fluid-derived stem cells (hAFSCs) on skin regeneration and photo-aging
- Establishment of a culture model for the prolonged maintenance of chicken feather follicles structure in vitro
- The Frequency of Alopecia and Quality of Life in High-School Students in Rural Areas (Sivrihisar, Mahmudiye, Alpu, Beylikova) of Eskisehir
- α-Mangostin, a safe and natural product as a candidate skin-whitening agent
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Evaluación de la seguridad de minoxidil oral a dosis bajas en el tratamiento de la alopecia
- Psychometric validation of the Spanish alopecia areata–life impact questionnaire
- Ritlecitinib in severe alopecia areata: a profile of its use
- Expanding the Senior-Løken syndrome spectrum: Combined Rothmund-Thomson features unveil the distinct Teelwani Syndrome phenotype
- Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis
- Sterile neutrophilic dermatitis in a cat - a case report
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Defective trophoblast function in mice with a targeted mutation of Ets2
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Nrf2-Mediated Expansion of Pilosebaceous Cells Accelerates Cutaneous Wound Healing
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Expression of Signaling Components in Embryonic Eyelid Epithelium
- Insights into male androgenetic alopecia using comparative transcriptome profiling: hypoxia-inducible factor-1 and Wnt/β-catenin signalling pathways
- Characterization of Rickets Type II Model Rats to Reveal Functions of Vitamin D and Vitamin D Receptor
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity