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- XEDAR activates the non-canonical NF-κB pathway
- The Roles of EDA2R in Ageing and Disease
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Store-operated calcium channels in skin
- Dysfunction of keratinocyte adhesion
- Edar Signaling in the Control of Hair Follicle Development
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Genetics of Structural Hair Disorders
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Biology and Genetics of Hair
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- <i>WNT10A</i> , dermatology and dentistry
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Current Genetics in Hair Diseases
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Skin Development and Disease: A Molecular Perspective
- Inherited Disorders of the Hair