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Research 631–660 of 1000+
- Unlocking the genetic secrets of Dorper sheep: insights into wool shedding and hair follicle development
- Stem-cell therapy in dermatology – Challenges and opportunities
- Application of Non-Pharmacologic Therapy in Hair Loss Treatment and Hair Regrowth
- Status of research on the development and regeneration of hair follicles
- The Role of ATP-dependent Chromatin Remodeling in the Control of Epidermal Differentiation and Skin Stem Cell Activity
- 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
- 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
- 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
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- KID Syndrome: Report of a Case and Support for Its Reclassification as an Ectodermal Dysplasia
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasia
- Molecular mechanisms of ectodermal dysplasia syndromes
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia