Search
for
Sort by
Research 241–270 of 1000+
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Antihypertensive Agents in Dermatology
- Author Index
- Subject Index
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Clinical features of taste disorders in Cronkhite-Canada syndrome: A report of 10 cases
- Twenty nail onychomadesis: An unusual finding in Cronkhite–Canada syndrome
- Cronkhite-Canada syndrome: A case report and literature review
- Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis
- Strange cutaneous abnormalities and polyposis in an Asiatic man
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Ectodermal Organ Stem Cells: Morphogenesis, Population Regenerative Behavior, and Evo-Devo
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Comparative Spatial Transcriptomic and Single-Cell Analyses of Human Nail Units and Hair Follicles Show Transcriptional Similarities between the Onychodermis and Follicular Dermal Papilla
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Hair, Wool, Quill, Nail, Claw, Hoof, and Horn
- 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