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Research 61–90 of 1000+
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Regulation of masculinization: androgen signalling for external genitalia development
- The Role of Histone Demethylases in Disease
- Gene Therapy: Recent Advances and Applications in Dermatology
- Two females with hair loss
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Congenital atrichia and hypotrichosis
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Epigenetic control of adult stem cell function
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- Activation of the OVOL1-OVOL2 Axis in the Hair Bulb and in Pilomatricoma
- From basic biology to engineered therapies: the keratinocyte stem cell playbook
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Function of KLF4 in Stem Cell Biology
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Molecular heterogeneity of quiescent melanocyte stem cells revealed by single-cell RNA-sequencing
- A preliminary study of finasteride in Tourette syndrome
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Removing all obstacles: A critical role for p53 in promoting tissue renewal
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase