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- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Genetic mapping of hair loss through the APCDD1 gene pathway: A new perspective
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- Biology and Genetics of Hair
- Dynamic Signals for Hair Follicle Development and Regeneration
- Congenital hair loss disorders: Rare, but not too rare
- Genetics of Structural Hair Disorders
- Inherited Disorders of the Hair
- Current Genetics in Hair Diseases
- Genetics of Alopecia
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- The Pathogenesis and Treatment Progress of Androgenic Alopecia
- 189 Integrating single-cell and spatial transcriptomics of human hair follicles to define transcriptional signature of follicular dermal papilla
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- News in brief
- DNCB 유발 피부염 생쥐에서 보스웰리아가 피부조직 모발주기 관련 유전자에 미치는 영향
- A Comparative study of Regulations of Cell and Gene therapy in US, EU and India
- Signaling Involved in Hair Follicle Morphogenesis and Development
- Trichoscopy for common hair loss diseases: Algorithmic method for diagnosis
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- The Mesenchymal Niche of the Hair Follicle Induces Regeneration by Releasing Primed Progenitors from Inhibitory Effects of Quiescent Stem Cells
- Identification of transcriptional targets of Wnt/β-catenin signaling in dermal papilla cells of human scalp hair follicles: EP2 is a novel transcriptional target of Wnt3a
- An Intrinsic Oscillation of Gene Networks Inside Hair Follicle Stem Cells: An Additional Layer That Can Modulate Hair Stem Cell Activities
- Defining the identity of mouse embryonic dermal fibroblasts
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient
- Molecular Genetics of Alopecias
- Human Fetal Scalp Dermal Papilla Enriched Genes and the Role of R-Spondin-1 in the Restoration of Hair Neogenesis in Adult Mouse Cells