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Research 811–840 of 1000+
- 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
- Hypotrichosis congenita of Marie Unna
- 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