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Research 361–390 of 1000+
- Transgenic mice provide new insights into the role of TGF-alpha during epidermal development and differentiation.
- Utilization of Stem Cells in Medicine: A Narrative Review
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Establishment of Tsc2-deficient rat embryonic stem cells
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Mesenchymal Stem Cells for the Treatment of Skin Diseases
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Advances in hair growth
- Protective Effect of Conditioned Medium of Immortalized Human Stem Cells from Exfoliated Deciduous Teeth Against Hair Graying Caused by X-Ray Irradiation via Its Antioxidative Activity
- Stem-cell therapy in dermatology – Challenges and opportunities
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- 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
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Ectoderm-Targeted Overexpression of the Glucocorticoid Receptor Induces Hypohidrotic Ectodermal Dysplasia
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Salivary gland function in persons with ectodermal dysplasias
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Scaffold-based developmental tissue engineering strategies for ectodermal organ regeneration
- Alopecia in congenital hidrotic ectodermal dysplasia responding to treatment with a combination of topical minoxidil and tretinoin
- Loss of a homologous group of proteins in a dominantly inherited ectodermal malformation
- Topical minoxidil treatment for congenital alopecia in hypohidrotic ectodermal dysplasia
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation