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Research 61–90 of 1000+
- The Genetics of Human Skin Disease
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Connexin mutations in human disease
- Progeroide Syndrome
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Stem Cell Competition for Niche Occupancy: Emerging Themes and Mechanisms
- PandaOmics: An AI-Driven Platform for Therapeutic Target and Biomarker Discovery
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Endocrine care of transpeople part I. A review of cross-sex hormonal treatments, outcomes and adverse effects in transmen
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Biochemistry of epidermal stem cells
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Mutation of the GDP-Fucose Biosynthesis Gene gmds Increases Hair Cell Number and Neuromast Regenerative Capacity in Zebrafish
- MICRO-URZĄDZENIA, BEZPRZEWODOWE KAPSUŁKI, MAPY, STYMULATORY I ROZRUSZNIKI STOSOWANE DO DIAGNOSTYKI I LECZENIA ZABURZEŃ MOTORYKI PRZEWODU POKARMOWEGO
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)
- IL-36γ drives skin toxicity induced by EGFR/MEK inhibition and commensal Cutibacterium acnes
- Chemistry42: An AI-Driven Platform for Molecular Design and Optimization
- Intrinsic ROS Drive Hair Follicle Cycle Progression by Modulating DNA Damage and Repair and Subsequently Hair Follicle Apoptosis and Macrophage Polarization
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Keratin-6 driven ODC expression to hair follicle keratinocytes enhances stemness and tumorigenesis by negatively regulating Notch