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Research 151–180 of 1000+
- Comparative Anatomy of Mouse and Human Nail Units
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- When whorls collide: the development of hair patterns in frizzled 6 mutant mice
- Activin B Stimulates Mouse Vibrissae Growth and Regulates Cell Proliferation and Cell Cycle Progression of Hair Matrix Cells through ERK Signaling
- Long-Term Bezafibrate Treatment Improves Skin and Spleen Phenotypes of the mtDNA Mutator Mouse
- The human keratins: biology and pathology
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Sic Transit Gloria: Farewell to the Epidermal Transit Amplifying Cell?
- Pathology of Mouse Models of Accelerated Aging
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Specific morphogenetic events in mouse external genitalia sex differentiation are responsive/dependent upon androgens and/or estrogens
- Field Cancerization: From Molecular Basis to Selective Field-Directed Management of Actinic Keratosis
- Peripheral MC1R Activation Modulates Immune Responses and is Neuroprotective in a Mouse Model of Parkinson’s Disease
- Rapid Genetic Analysis of Epithelial-Mesenchymal Signaling During Hair Regeneration
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Obesity resistance of the stearoyl-CoA desaturase-deficient (<i>scd1</i> <sup>-/-</sup>) mouse results from disruption of the epidermal lipid barrier and adaptive thermoregulation
- Role of the Notch Ligand Delta1 in Embryonic and Adult Mouse Epidermis
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Evaluation of Animal Models Suitable for Hair Research and Regeneration
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Current Protocols: Alopecia Areata Mouse Models for Drug Efficacy and Mechanism Studies
- An <i>mTurq2-Col4a1</i> mouse model allows for live visualization of mammalian basement membrane development