Search
for
Sort by
Research 841–870 of 1000+
- Effects of Collagen Peptides on Gene Expression Related to Hair Cycle Activation in the Skin
- 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
- 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
- Current Genetics in Hair Diseases
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Investigating the roles of cellular senescence in embryogenesis and aging
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- Clinical Snippets
- Clouston syndrome associated with eccrine syringofibroadenoma
- 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
- Clinical case of alopecia totalis in pediatric practice
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Research Snippets
- Hedgehog and Gli Signaling in Embryonic Mammary Gland Development
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- sQuiz your knowledge: Polycyclic annular plaques on the trunk following dutasteride treatment
- Identification of a secreted BMP antagonist, ectodin, integrating BMP, FGF, and SHH signals from the tooth enamel knot
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Molecular biology of hair morphogenesis: Development and cycling
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome