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Research 571–600 of 1000+
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- 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
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Molecular biology of hair morphogenesis: Development and cycling
- 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
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- 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
- Hair: more than just an appendage
- Hypotrichosis congenita of Marie Unna
- Transcriptomic landscape of early hair follicle and epidermal development
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- 1418 Characterization of ectomesenchyme as an origin of epidermal stem cells
- Comprehensive treatment of Cronkhite-Canada syndrome: A case report and literature review
- Varicella Recurrence Complicated by Pneumonia After Liver Transplantation for APECED
- 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
- Cronkhite-Canada syndrome: A case report and literature review
- Hair Loss and Polyposis in Cronkhite-Canada Syndrome
- Decellularized Wharton's jelly matrix as a three dimensional scaffold for wound healing and hair regeneration applications
- New-Onset Gastrointestinal Polyposis
- Signaling pathways involved in hair follicle cycling and morphogenesis
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- P63 expression pattern during rat epidermis morphogenesis and the role of p63 as a marker for epidermal stem cells
- Reptile scale paradigm: Evo-Devo, pattern formation and regeneration