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Research 631–660 of 1000+
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Skin, Genetic Defects, and Aging
- Hair Anomalies in a 6-Year-Old Girl
- Genetics of Alopecia
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Real-world single-center experience with 10 cases of generalized pustular psoriasis successfully treated with ixekizumab
- GTL1 is required for a robust root hair growth response to avoid nutrient overloading
- Remodelling of cytoskeleton and plasma membrane proteins contributes to drought sensitivity of Arabidopsis<i>rhd2</i>mutant
- The Endocrine Function of the Skin: An Analytical Narrative
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Frizzled Receptors in Development and Disease
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- Skin morphology of the mutant hairless USP mouse
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- WNT Signaling in Disease
- Pathology of Mouse Models of Accelerated Aging
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Roles of the Hedgehog Signaling Pathway in Epidermal and Hair Follicle Development, Homeostasis, and Cancer
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Skin Development and Disease: A Molecular Perspective
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Proteomic Analysis of Two Stem Cell Secretomes Used in Combination in a Topical Skin Care Product That Has Demonstrated Efficacy in a Double-Blinded, Vehicle-Controlled Clinical Trial
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Ectodermal Dysplasia: Variable Expressions