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- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Genetics of Alopecia
- An Extended Epidermal Response Heals Cutaneous Wounds in the Absence of a Hair Follicle Stem Cell Contribution
- 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
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Inherited Disorders of the Hair
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Current Genetics in Hair Diseases
- Biology and Genetics of Hair
- Obtaining a Dermocosmetics from the aerial parts of Eclipta alba (L.) for the treatment of alopecia / Obtenção de um Dermocosmético das partes aéreas de Eclipta alba (L.) para o tratamento da alopecia
- ANAIS DO I CONGRESSO MÉDICO DE FORMOSA - COMEF
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Wound Healing and Skin Regeneration
- Signaling Involved in Hair Follicle Morphogenesis and Development
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators
- Epithelial stem cells and implications for wound repair
- Signaling in the stem cell niche: regulating cell fate, function and plasticity
- Epidermal β-catenin activation remodels the dermis via paracrine signalling to distinct fibroblast lineages
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- 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
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Trichoscopy in Hair Shaft Disorders