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- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- The nude gene and the skin
- Learning from nudity: lessons from the nude phenotype
- FOXN1 deficient nude severe combined immunodeficiency
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- miR-3606-3p alleviates skin fibrosis by integratively suppressing the integrin/FAK, p-AKT/p-ERK, and TGF-β signaling cascades
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- P‐30 Use of fipronil for treatment of <i>Lynxacarus radovskyi</i> in outdoor cats in Rio de Janeiro (Brazil)
- P‐81 A retrospective study of equine sarcoidosis
- Fetal wound healing using a genetically modified murine model: the contribution of P-selectin
- Accumulations of Ca/P in the core of hairs from Taklamakan desert mummies
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- Regulation of immune response genes in the skin of allergic and clinically tolerant individuals exposed to p‐phenylenediamine
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- P latelet rich plasma application by dermapen microneedling and intradermal point‐by‐point injection methods, and their comparison with clinical findings and trichoscan in patients with androgenetic alopecia
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>
- P‐79 Hair follicle growth arrest in Austrian Icelandic horses
- P‐46 A placebo‐controlled, double‐blinded study of recombinant IFNγ in dogs with atopic dermatitis
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- P‐35 Nonlethal junctional epidermolysis bullosa in a dog
- A bio-polymeric scaffold incorporated with p-Coumaric acid enhances diabetic wound healing by modulating MMP-9 and TGF-β3 expression
- 608 A clinical study to test the efficacy of VB1953 in clindamycin non-responder acne patients with antibiotic-resistant P. acnes
- FINASTERIDE INFLUENCE ON P-GLYCOPROTEIN FUNCTIONAL ACTIVITY