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Research 721–750 of 1000+
- AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity
- Cell Type-specific Functions of the Lysosomal Protease Cathepsin L in the Heart
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Recently Identified Forms of Epidermolysis Bullosa
- Central centrifugal cicatricial alopecia: challenges and solutions
- Hair follicle stem cell replication stress drives IFI16/STING-dependent inflammation in hidradenitis suppurativa
- Rab5c-mediated endocytic trafficking regulates hematopoietic stem and progenitor cell development via Notch and AKT signaling
- Elucidating the roles of three β-glucuronosyltransferases (GLCATs) acting on arabinogalactan-proteins using a CRISPR-Cas9 multiplexing approach in Arabidopsis
- The role of WNT10B in physiology and disease: A 10-year update
- Congenital adrenal hyperplasia
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Alopecia Areata
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Advances in single-cell transcriptomics in animal research
- Palatogenesis and cutaneous repair: A two‐headed coin
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- Retinoids for Chemoprophylaxis of Nonmelanoma Skin Cancer
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- The Yin and Yang of Integrin Function in Re-Epithelialization During Wound Healing
- Diseases of Periocular Hair
- Dual-Action Icariin-Containing Thermosensitive Hydrogel for Wound Macrophage Polarization and Hair-Follicle Neogenesis
- Disorders of hair
- Wnt/β-Catenin Signaling Stabilizes Hemidesmosomes in Keratinocytes
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response