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Research 121–150 of 1000+
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Reversible Activation of c-Myc in Skin
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- A Hairy Cituation – PADIs in Regeneration and Alopecia
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Dermatologic Manifestations of Mitochondrial Dysfunction: A Review of the Literature
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Molecular Mechanisms Regulating Hair Follicle Development
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Montagna Symposium 2014—Skin Aging: Molecular Mechanisms and Tissue Consequences
- Diagnosis and Management of Melanoma of the Scalp: A Review of the Literature
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- The Rho GTPase exchange factor Vav2 promotes extensive age-dependent rewiring of the hair follicle stem cell transcriptome
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- An Update of Congenital Adrenal Hyperplasia
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Genetic Defects of Female Sexual Differentiation
- 46,XY DSD due to impaired androgen production