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- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Current Genetics in Hair Diseases
- Genetics of Alopecia
- Biology and Genetics of Hair
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation
- Inherited Disorders of the Hair
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Hair shaft structures in EDAR induced ectodermal dysplasia
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Combination of Transcriptomics and Proteomics Reveals Differentially Expressed Genes and Proteins in the Skin of EDAR Gene-Targeted and Wildtype Cashmere Goats
- <i>WNT10A</i> , dermatology and dentistry
- In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators
- Regeneration of skin appendages and nerves: current status and further challenges
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Genetic Hair Disorders: A Review
- Rhamnose-mediated modulation of hair follicle growth: insights from chemical genomics
- Fondation René Touraine
- Molecular Mechanisms Affecting Development of Animal Fibers and Some Studies on Goats
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co-option in the evolution of the hair follicle
- Loss of ‘Epidermal Melanin Unit’ Integrity in Human Skin During Melanoma-Genesis
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- An Extended Epidermal Response Heals Cutaneous Wounds in the Absence of a Hair Follicle Stem Cell Contribution