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- Uncombable hair syndrome and beyond
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Oral pathology: Clinical pathologic correlations (ed 3)
- Trichorrhexis Nodosa After Hair Transplantation: Dermoscopic, Pathologic and Electron Microscopy Analyses
- Autologous Stem Cell-derived Therapies for Androgenetic Alopecia: A Systematic Review of Randomized Control Trials on Efficacy, Safety, and Outcomes
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Short Anagen Syndrome in an Indian Woman with its Impact on Quality-of-Life
- Physiological and biological skin changes in pregnancy
- Scaffold-based developmental tissue engineering strategies for ectodermal organ regeneration
- <i>WNT10A</i> , dermatology and dentistry
- An animal study on the effectiveness of platelet-rich plasma as a direct pulp capping agent
- Dermatology and Pregnancy
- Ectodermal Organ Stem Cells: Morphogenesis, Population Regenerative Behavior, and Evo-Devo
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Chronic telogen effluvium is due to a reduction in the variance of anagen duration
- Contribution of androgens to chronic allograft nephropathy is mediated by dihydrotestosterone
- The role of WNT10B in physiology and disease: A 10-year update
- Ptch2 is a Potential Regulator of Mesenchymal Stem Cells
- Global research trends in non-muscle invasive bladder cancer: Bibliometric and visualized analysis
- Structural Abnormalities in the Hair of a Patient with a Novel Ribosomopathy
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Control by a hair’s breadth: the role of microRNAs in the skin
- Human Liver MSCs Retain Their Basic Cellular Properties in Chronically Inflamed Liver Tissue
- Understanding skin morphogenesis across developmental, regenerative and evolutionary levels
- Mesenchymal Stem Cell Secretome: Toward Cell-Free Therapeutic Strategies in Regenerative Medicine
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway