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Research 631–660 of 1000+
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Cell fate decisions: emerging roles for metabolic signals and cell morphology
- SOX9 in organogenesis: shared and unique transcriptional functions
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Immune therapies for alopecia areata: evidence and new perspectives
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- HPV8 Field Cancerization in a Transgenic Mouse Model Is due to Lrig1+ Keratinocyte Stem Cell Expansion
- NF-κB Activity Is Required for Anagen Maintenance in Human Hair Follicles In Vitro
- Differences between ultrastructure and protein composition in straight hair fibres
- Temporal Triangular Alopecia – A Diagnostic Dilemma: Case Series of Six Patients
- Fresh Umbilical Cord Blood—A Source of Multipotent Stem Cells, Collection, Banking, Cryopreservation, and Ethical Concerns
- New-Onset Gastrointestinal Polyposis
- 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
- 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
- Transcriptome and proteome characterization of surface ectoderm cells differentiated from human iPSCs
- 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