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Research 811–840 of 1000+
- Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Congenital Atrichia: A Case Report
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Molecular Basis of Hereditary Hair Diseases
- 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages
- Dermatological diseases from a genetic perspective
- Mediator 1 ablation induces enamel-to-hair lineage conversion through enhancer dynamics
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- Clouston’s syndrome: a rare case report
- The Naked (N) Mutation, Chromosome 15
- Index
- Strange cutaneous abnormalities and polyposis in an Asiatic man
- Hair Loss in Children, Etiologies, and Treatment
- El teorema del 0,7 o el otro teorema de Pitágoras
- N02. Hair and Nails
- Identification of Ectodysplasin Target Genes Reveals the Involvement of Chemokines in Hair Development
- Expression of <i>Foxi3</i> is regulated by ectodysplasin in skin appendage placodes
- Suppression of hair follicle development inhibits induction of sonic hedgehog, patched, and patched-2 in hair germs in mice
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Inherited Disorders of the Hair
- Investigating the roles of cellular senescence in embryogenesis and aging
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- Clinical Snippets
- Keratin disorders: from gene to therapy
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- XEDAR activates the non-canonical NF-κB pathway
- A new type of pachyonychia congenita.
- Ugreelig hår