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Research 511–540 of 1000+
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Telogen hair loss
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Wnt/β-Catenin Signaling Stabilizes Hemidesmosomes in Keratinocytes
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- The molecular basis of human keratin disorders
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- Keratinocyte-derived follistatin regulates epidermal homeostasis and wound repair
- Genetically separable determinants of hair keratin gene expression
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- New developments in the molecular treatment of ichthyosis: review of the literature
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Loss of Dicer in Newborn Melanocytes Leads to Premature Hair Graying and Changes in Integrin Expression
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Antiviral drugs prolong survival in murine recessive dystrophic epidermolysis bullosa
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep