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- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- The Roles of EDA2R in Ageing and Disease
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- Ectodermal Dysplasia: Variable Expressions
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Research Snippets
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Biology and Genetics of Hair
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Current Genetics in Hair Diseases
- Edar Signaling in the Control of Hair Follicle Development
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- <i>WNT10A</i> , dermatology and dentistry