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Research 691–720 of 1000+
- The amazing miniorgan: Hair follicle
- Anatomy and Biology of Hair at Different Ages
- Structural and Pigmentary Characteristics of the Skin in Hairless Dog Breeds
- Clinical features of taste disorders in Cronkhite-Canada syndrome: A report of 10 cases
- Mediator 1 ablation induces enamel-to-hair lineage conversion through enhancer dynamics
- Strange cutaneous abnormalities and polyposis in an Asiatic man
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- Onset of Keratin 17 Expression Coincides with the Definition of Major Epithelial Lineages during Skin 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
- Integumentary System
- Effects of Collagen Peptides on Gene Expression Related to Hair Cycle Activation in the Skin
- Generation and characterization of hair-bearing skin organoids from human pluripotent stem cells
- Investigating the roles of cellular senescence in embryogenesis and aging
- 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>
- Identification of a secreted BMP antagonist, ectodin, integrating BMP, FGF, and SHH signals from the tooth enamel knot
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Gain‐of‐function variants in the <i>ODC1</i> gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities
- Hair: more than just an appendage
- Hypotrichosis congenita of Marie Unna
- Transcriptomic landscape of early hair follicle and epidermal development
- 1418 Characterization of ectomesenchyme as an origin of epidermal stem cells
- Comprehensive treatment of Cronkhite-Canada syndrome: A case report and literature review
- Exome analysis for Cronkhite-Canada syndrome: A case report
- Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
- Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis