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Research 541–570 of 1000+
- Programmable viscoelastic hydrogels exhibit antimicrobial and regenerative properties to promote cell migration, wound healing, and tissue remodeling
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Dermal Delivery of Topically Applied Oligonucleotides via Follicular Transport in Mouse Skin
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Case report: NUDT15 polymorphism and severe azathioprine-induced myelosuppression in a young Chinese female with systematic lupus erythematosus: a case analysis and literature review
- Variation in the ovine trichohyalin gene and its association with wool curvature
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Ovine KRT81 Variants and Their Influence on Selected Wool Traits of Commercial Value
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- S100A6: molecular function and biomarker role
- Self-consistent field theory for the interactions between keratin intermediate filaments
- Identification and Analysis of MYB Gene Family for Discovering Potential Regulators Responding to Abiotic Stresses in Curcuma wenyujin
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Mesenchymal Stem Cells With Modification of Junctional Adhesion Molecule A Induce Hair Formation
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- The Catalog of Human Hair Keratins
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Immunization by Application of DNA Vaccine onto a Skin Area Wherein the Hair Follicles Have Been Induced into Anagen-onset Stage
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Regulation of Keratin Gene Expression in Hair Follicle Differentiation<sup>a</sup>
- Organization and Expression of Hair Follicle Genes.
- Sequence, expression, and evolutionary conservation of a gene encoding a glycine/tyrosine-rich keratin-associated protein of hair.
- Allosteric interactions prime androgen receptor dimerization and activation