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- Dysfunction of keratinocyte adhesion
- A direct link between<i>Prss53</i>, hair curvature, and skeletal dysplasia
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Epidermal field carcinogenesis in bald-headed: An attempt at finetuning early non-invasive detection
- Mutant Cx43 in Skin Differentiation and Disease
- Store-operated calcium channels in skin
- Abnormal differentiation of epidermis in transgenic mice constitutively expressing cyclooxygenase-2 in skin
- Research Snippets
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- Analysis of proliferation, apoptosis and keratin expression in cultured normal and immortalized human buccal keratinocytes
- CD271 orchestrates skin structure, differentiation, and inflammation via PI3K/Akt and PKCα/ERK pathways
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Selenoproteins Are Essential for Proper Keratinocyte Function and Skin Development
- Pharmacological activation of estrogen receptors-α and -β differentially modulates keratinocyte differentiation with functional impact on wound healing
- A Mouse Model for Conditional Expression of Activated β-Catenin in Epidermal Keratinocytes
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Dermatopathology and molecular genetics
- N02. Hair and Nails
- Polarized microscopy in genetic hair disorders: case series
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- BH03: Systemic sclerosis and frontal fibrosing alopecia: a novel combination of scarring alopecia