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Research 211–240 of 1000+
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Influence of feed restriction on the wool proteome: A combined iTRAQ and fiber structural study
- Production of artificial synthetic spidroin gene 4S-transgenic cloned sheep embryos using somatic cell nuclear transfer
- Special Biochemical Features of the Hair Follicle
- Ribonucleic Acids Coding for the Keratin Complex of Hair
- Assessment of the skin efficacy and acceptability of a cosmetic product in the treatment of the forearm hypertrichosis in female patients
- Brief study of hypertrichosis
- The effects of hydrophobic modifications on the interaction of human hair with water
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses
- Potential of fermented small black soybean-lactobacillus complex for hair health: a study on hair growth and follicle gene expression
- Spinal bicuculline produces hypersensitivity of dorsal horn neurons: effects of excitatory amino acid antagonists
- Biosynthesis and function of rhizobacterial secondary metabolites in plant abiotic stress tolerance
- Hair growth rate estimation in North American ursids
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Effect of Hataedock Treatment on Epidermal Structure Maintenance through Intervention in the Endocannabinoid System
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Structure and expression of genes for a class of cysteine-rich proteins of the cuticle layers of differentiating wool and hair follicles.
- 5 alpha-reductase-2 gene mutations in the Dominican Republic.
- Levetiracetam in the Treatment of Idiopathic Generalized Epilepsies
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- A guide to diagnosis and management of hypertrichosis
- Functional Characterization of<i>fer-ts</i>, a Temperature-Sensitive FERONIA Mutant Allele That Alters Root Hair Growth
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- 1385 Characterizing the expression of metabolic markers in alopecia areata
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- Wnt and Notch signaling pathway involved in wound healing by targeting c-Myc and Hes1 separately