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Research 451–480 of 1000+
- Ichthyosis
- FOXN1 deficient nude severe combined immunodeficiency
- T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- GRowing an Epidermal Tumor
- Approach to androgen excess in women: Clinical and biochemical insights
- Gene-knockout mice with abnormal epidermal and hair follicular development
- “Structural imprinting” of the cutaneous immune effector function
- Tissue Engineering in Cosmetics and Dermatology: A New Era of Innovation and Application
- Author reply
- Evaluating 5 alpha reductase inhibitors for the treatment of male androgenic alopecia
- Hypotrichosis in a child with olmsted syndrome
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Dermatopathy in juvenile Angus cattle due to vitamin A deficiency
- Clouston’s syndrome: a rare case report
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- An Approach to Hair Loss in Pediatric Primary Care
- A Review of the Most Common Dermatologic Conditions and their Debilitating Psychosocial Impacts
- Runx Family Genes in Tissue Stem Cell Dynamics
- Spatiotemporal Labeling of Melanocytes in Mice
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report