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Research 241–270 of 280
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Role of janus kinase inhibitors in the treatment of alopecia areata
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Immunology of alopecia areata
- Recombinant human hepatitis B vaccine initiating alopecia areata: testing the hypothesis using the C3H/HeJ mouse model
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Immunopathology and Immunotherapy of Inflammatory Skin Diseases
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Alopecia areata following COVID-19 vaccine: a systematic review
- Congenital atrichia with papular lesions
- Childhood Alopecia Areata: An Overview of Treatment and Recent Patents
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Genetic Control/Involvement in Hair Fiber Traits
- Desmogleins: Hair perspective
- Evolution, mechanism of action, and clinical applications of three generations of antihistamines
- Alopecia Areata after COVID-19 Vaccines
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Evaluation of serum ferritin, vitamin B12 and vitamin D levels as biochemical markers of chronic telogen effluvium in women
- Trichothiodystrophy
- Therapeutic update on alopecia areata: a critical review of standard and emerging targeted therapies