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Research 631–660 of 1000+
- Cronkhite–Canada Syndrome With Multiple Mesenteric Lymphadenopathy: A Case Report
- Summation and recommendations for the safe and effective use of topical and oral minoxidil
- A girl with loose anagen hair syndrome and concurrent uncombable hair syndrome
- Evolution of long scalp hair in humans
- The changing landscape of managing hair loss: a 30‐year perspective
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Temporal Triangular Alopecia – A Diagnostic Dilemma: Case Series of Six Patients
- Cell fate decisions: emerging roles for metabolic signals and cell morphology
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Early inductive events in ectodermal appendage morphogenesis
- Human Induced Pluripotent Stem Cell–Derived Ectodermal Precursor Cells Contribute to Hair Follicle Morphogenesis In Vivo
- 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
- FGF-9 accelerates epithelial invagination for ectodermal organogenesis in real time bioengineered organ manipulation
- Loss of a homologous group of proteins in a dominantly inherited ectodermal malformation
- Ectodermal Organ Stem Cells: Morphogenesis, Population Regenerative Behavior, and Evo-Devo
- Hair Follicle Organoids Using Human iPSC-Derived Ectodermal Precursor Cells for Hair Regenerative Medicine
- 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
- Transcriptome and proteome characterization of surface ectoderm cells differentiated from human iPSCs
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- Overcoming genetic drivers in alopecia areata: hair regrowth in a patient with <i>AIRE</i> gene mutation (autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy, APECED syndrome) treated with ruxolitinib
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Parallels in signaling between development and regeneration in ectodermal organs
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- 1435 Dynamic morphogen-p63 chromatin interactions that guide epigenetic changes and p63 activity in surface ectoderm commitment
- A Unique Case of Trichorrhexis Nodosa—"Bamboo Hairs"