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Research 181–210 of 1000+
- PA33 When bones speak through nails: insights from a paediatric case series
- Hair Evaluation in Orthodontic Patients with Oligodontia
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Hypotrichosis with juvenile macular dystrophy
- Cronkhite-Canada syndrome: A case report and literature review
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Specific morphogenetic events in mouse external genitalia sex differentiation are responsive/dependent upon androgens and/or estrogens
- Expression of Cyclooxygenase Isozymes During Morphogenesis and Cycling of Pelage Hair Follicles in Mouse Skin: Precocious Onset of the First Catagen Phase and Alopecia upon Cyclooxygenase-2 Overexpression
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Skin Development and Disease: A Molecular Perspective
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Congenital atrichia with papular lesions
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- The involvement of Elf5 in regulating keratinocyte proliferation and differentiation processes in skin
- Hypotrichosis in a child with olmsted syndrome
- Notch Signaling in Hair Follicle Development
- Defective trophoblast function in mice with a targeted mutation of Ets2
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- Targeted inactivation of integrin-linked kinase in hair follicle stem cells reveals an important modulatory role in skin repair after injury
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Phototherapy of androgenetic alopecia with low level narrow band 655-nm red light and 780-nm infrared light