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Research 691–720 of 1000+
- 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
- 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
- Signaling pathways involved in hair follicle cycling and morphogenesis
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- Skin-derived stem cells as a source of primordial germ cell- and oocyte-like cells
- 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
- Getting to the root of scales, feather and hair: As deep as odontodes?
- Generalized Hair-Follicle Hamartoma
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- Analysis of skin graft survival using green fluorescent protein transgenic mice
- Twenty nail onychomadesis: An unusual finding in Cronkhite–Canada syndrome
- Clinical presentations of alopecia areata
- Hair Evaluation in Orthodontic Patients with Oligodontia
- Assessment of the Embryological Origin, Anatomical and Histological Structure of the Skin
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co- option in the evolution of the hair follicle
- Adult Stem Cells as an Alternative Source of Multipotential (Pluripotential) Cells in Regenerative Medicine
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load