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Research 631–660 of 1000+
- SOX9 in organogenesis: shared and unique transcriptional functions
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- Immune therapies for alopecia areata: evidence and new perspectives
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Recent Advances in the Role of Fibroblast Growth Factors in Hair Follicle Growth
- E-Poster
- Fresh Umbilical Cord Blood—A Source of Multipotent Stem Cells, Collection, Banking, Cryopreservation, and Ethical Concerns
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- 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
- Functional ectodermal organ regeneration as the next generation of organ replacement therapy
- 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
- A Unique Case of Trichorrhexis Nodosa—"Bamboo Hairs"