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Research 871–900 of 1000+
- 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
- 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
- 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
- Genetic hair and nail disorders
- 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
- Skin-derived stem cells as a source of primordial germ cell- and oocyte-like 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
- A New Case of Isolated Trichothiodystrophy
- 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
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Congenital atrichia associated with situs inversus and mesocardia
- Hair Evaluation in Orthodontic Patients with Oligodontia