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Research 301–330 of 1000+
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- Wnt Signaling in Skin Development, Homeostasis, and Disease
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Pharmacological Activation of Thermo–Transient Receptor Potential Vanilloid 3 Channels Inhibits Hair Growth by Inducing Cell Death of Hair Follicle Outer Root Sheath
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Data from Synergistic Function of Smad4 and PTEN in Suppressing Forestomach Squamous Cell Carcinoma in the Mouse
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- WNT10B (wingless-type MMTV integration site family)
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- Insulin Resistance and Polycystic Ovary Syndrome
- The Inflammatory Caspases-1 and -11 Mediate the Pathogenesis of Dermatitis in Sharpin-Deficient Mice
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Pannexin 3 regulates skin development via Epiprofin
- NUDT15 polymorphism explains serious toxicity to azathioprine in Indian patients with chronic immune thrombocytopenia and autoimmune hemolytic anemia: a case series
- AIMP1-Derived Peptide Secreted from Hair Follicle Stem Cells Promotes Hair Growth by Activating Dermal Papilla Cells
- Darier Sign: A Historical Note
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- A Case of Azathioprine Induced Severe Myelosuppression and Alopecia Totalis in IgA Nephropathy
- Acne
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Macrophages Contribute to the Cyclic Activation of Adult Hair Follicle Stem Cells
- The roles of Wnt/β‐catenin pathway in tissue development and regenerative medicine
- Hyperadrenocorticism in Ferrets
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene