Search
for
Sort by
Research 241–270 of 1000+
- Molecular Genetics of Human Hair Diseases
- TONGUE, RED
- Acanthosis nigricans, insulin resistance and cutaneous virilism
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Medical Dermatology
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Matriptase: Potent Proteolysis on the Cell Surface
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Human Peptidylarginine Deiminase Type III: Molecular Cloning and Nucleotide Sequence of the cDNA, Properties of the Recombinant Enzyme, and Immunohistochemical Localization in Human Skin
- Nanoparticles for Topical Application in the Treatment of Skin Dysfunctions—An Overview of Dermo-Cosmetic and Dermatological Products
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- The regulation of skin homeostasis, repair and the pathogenesis of skin diseases by spatiotemporal activation of epidermal mTOR signaling
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- Stem Cells behind the Barrier
- Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis
- Cell death in skin function, inflammation, and disease
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin