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Research 271–300 of 1000+
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Evolution of Trichocyte Keratins
- Anti-invasive effects of minoxidil on human breast cancer cells: combination with ranolazine
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Corticotropin releasing hormone and the skin
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- RAGE and Its Ligands in Melanoma
- The molecular basis of human keratin disorders
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Keratinocyte-derived follistatin regulates epidermal homeostasis and wound repair
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Chronic delayed-type hypersensitivity reaction as a means to treat alopecia areata
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Proteolysis‐Targeting Chimera (PROTAC): Current Applications and Future Directions
- CD44 signaling in skin wound healing and regeneration
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Premature aging syndromes: From patients to mechanism
- Malignant Melanoma and Its Stromal Nonimmune Microecosystem
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain