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Research 121–150 of 1000+
- Dermal β-catenin activity in response to epidermal Wnt ligands is required for fibroblast proliferation and hair follicle initiation
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Specific morphogenetic events in mouse external genitalia sex differentiation are responsive/dependent upon androgens and/or estrogens
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Eyebrow Loss
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Ossifying pilomatrixoma with marrow formation of the left cheek region – Case report with review of literature
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- Temporal Triangular Alopecia – A Diagnostic Dilemma: Case Series of Six Patients
- Research progress in the treatment of non-scarring alopecia: mechanism and treatment
- Author Index
- Hox genes in development and beyond
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- E-Poster
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Early inductive events in ectodermal appendage morphogenesis
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes