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Research 961–990 of 1000+
- Recent Advances in the Role of Fibroblast Growth Factors in Hair Follicle Growth
- Stem-cell therapy in dermatology – Challenges and opportunities
- Application of Non-Pharmacologic Therapy in Hair Loss Treatment and Hair Regrowth
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- M-CSF-stimulated myeloid cells can convert into epithelial cells to participate in re-epithelialization and hair follicle regeneration during dermal wound healing
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- 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
- 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
- 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
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Ectodermal Dysplasia: Variable Expressions
- Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report.