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Research 241–270 of 1000+
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Approach to Alopecia in Dogs in Clinical Practice
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- 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
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- The Naked (N) Mutation, Chromosome 15
- Index
- Hair Loss in Children, Etiologies, and Treatment
- El teorema del 0,7 o el otro teorema de Pitágoras
- N02. Hair and Nails
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages
- Clouston’s syndrome: a rare case report
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Transcriptional activation of a subset of hair keratin genes by the NF-κB effector p65/RelA
- Disorders of the Hair and Scalp in Children
- Dermatological diseases from a genetic perspective
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Ectodysplasin research—Where to next?
- The Roles of EDA2R in Ageing and Disease
- Edar Signaling in the Control of Hair Follicle Development
- 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
- Store-operated calcium channels in skin
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases