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Research 271–300 of 1000+
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- 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 Cronkhite-Canada syndrome
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Cronkhite-Canada syndrome: A rare disease presenting with dermatological and gastrointestinal manifestations
- Using High-Throughput Immunoblotting to Identify Proteins Involved in the Differentiation of ES Cells along the Hair Follicle Lineage in Vitro
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- <i>Hoxc13</i> mutant mice lack external hair
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Cronkhite-Canada syndrome associated with colon cancer metastatic to liver
- Exome analysis for Cronkhite-Canada syndrome: A case report
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- An Unusual Case of Diarrhea, Dysgeusia, and Grainy and Nodular Mucosa
- Spontaneous improvement of Cronkhite-Canada syndrome in a postpartum female
- Cronkhite–Canada syndrome: from clinical features to treatment
- Understanding skin morphogenesis across developmental, regenerative and evolutionary levels
- Comprehensive treatment of Cronkhite-Canada syndrome: A case report and literature review
- “Review on premature white and grey hair in children.”
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- Smad1 and 5 but Not Smad8 Establish Stem Cell Quiescence Which Is Critical to Transform the Premature Hair Follicle During Morphogenesis Toward the Postnatal State
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin
- Induction of hair follicle dermal papilla cell properties in human induced pluripotent stem cell-derived multipotent LNGFR(+)THY-1(+) mesenchymal cells
- Transcriptome and proteome characterization of surface ectoderm cells differentiated from human iPSCs
- An Intrinsic Oscillation of Gene Networks Inside Hair Follicle Stem Cells: An Additional Layer That Can Modulate Hair Stem Cell Activities
- Disorders of hair in children
- brief review on “Herbal Hair Tonic”