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Research 631–660 of 1000+
- Differentiation of Mouse Induced Pluripotent Stem Cells into a Multipotent Keratinocyte Lineage
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Characterization of the serotoninergic system in the C57BL/6 mouse skin
- Controlled Delivery of T-box21 Small Interfering RNA Ameliorates Autoimmune Alopecia (Alopecia Areata) in a C3H/HeJ Mouse Model
- A novel mouse model demonstrates that oncogenic melanocyte stem cells engender melanoma resembling human disease
- Direct conversion of mouse and human fibroblasts to functional melanocytes by defined factors
- The C3H/HeJ mouse and DEBR rat models for alopecia areata: review of preclinical drug screening approaches and results
- An In Vivo Mouse Excisional Wound Model of Scarless Healing
- Three cDNA sequences of mouse type I keratins. Cellular localization of the mRNAs in normal and hyperproliferative tissues.
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Comparative Anatomy of Mouse and Human Nail Units
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Specific morphogenetic events in mouse external genitalia sex differentiation are responsive/dependent upon androgens and/or estrogens
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- A nude mouse model of hypertrophic scar shows morphologic and histologic characteristics of human hypertrophic scar
- Disruption of Smad4 in Mouse Epidermis Leads to Depletion of Follicle Stem Cells
- Long-Term Bezafibrate Treatment Improves Skin and Spleen Phenotypes of the mtDNA Mutator Mouse
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Gene Expression of Mouse S100A3, a Cysteine-Rich Calcium-Binding Protein, in Developing Hair Follicle
- Optimal skin regeneration after full thickness thermal burn injury in the spiny mouse, Acomys cahirinus
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Hair corticosterone measurement in mouse models of type 1 and type 2 diabetes mellitus
- Blimp1+ cells generate functional mouse sebaceous gland organoids in vitro
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Senescence-accelerated Mouse (SAM): With Special Reference to Development and Pathobiological Phenotypes
- Wnt10b Promotes Differentiation of Mouse Hair Follicle Melanocytes
- Prevention and treatment of alopecia areata with quercetin in the C3H/HeJ mouse model
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5