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Research 781–810 of 1000+
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- Hair structure anatomy and comparative anatomy1 1Dedicated to the memory of the late Dr. R. E. Rivett whose untimely death prevented his role in co-authorship.
- Expression of COUP-TF-interacting protein 2 (CTIP2) in mouse skin during development and in adulthood
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- HOXC8 initiates an ectopic mammary program by regulating Fgf10 and Tbx3 expression, and Wnt/β-catenin signaling
- Integumentary System
- Effects of Collagen Peptides on Gene Expression Related to Hair Cycle Activation in the Skin
- Suppression of hair follicle development inhibits induction of sonic hedgehog, patched, and patched-2 in hair germs in mice
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Inherited Disorders of the Hair
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Investigating the roles of cellular senescence in embryogenesis and aging
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- Clinical Snippets
- Clouston syndrome associated with eccrine syringofibroadenoma
- Keratin disorders: from gene to therapy
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- XEDAR activates the non-canonical NF-κB pathway
- A new type of pachyonychia congenita.
- Ugreelig hår
- Clinical case of alopecia totalis in pediatric practice
- Hedgehog and Gli Signaling in Embryonic Mammary Gland Development
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- sQuiz your knowledge: Polycyclic annular plaques on the trunk following dutasteride treatment
- Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners.
- Identification of a secreted BMP antagonist, ectodin, integrating BMP, FGF, and SHH signals from the tooth enamel knot
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Gain‐of‐function variants in the <i>ODC1</i> gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks