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Research 901–930 of 1000+
- Ernährungsstörungen des Haares und deren Management
- The potential application of natural products in cutaneous wound healing: A review of preclinical evidence
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Cell death in skin function, inflammation, and disease
- Regulatory T cells in skin utilize the Cxcr4-Cxcl12 axis to promote hair follicle regeneration
- The Human Type II Keratin Gene Cluster on Chromosome 12q13.13: Final Count or Hidden Secrets?
- Sequences and differential expression of three novel human type-II hair keratins
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Structure and site of expression of a murine type II hair keratin
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Characterization of New Members of the Human Type II Keratin Gene Family and a General Evaluation of the Keratin Gene Domain on Chromosome 12q13.13
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- In vitro assembly properties of human type I and II hair keratins
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- Novel Type I Hair Keratins K39 and K40 Are the Last to be Expressed in Differentiation of the Hair: Completion of the Human Hair Keratin Catalog
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- A cDNA encoding the human type I hair keratin hHa1
- Keratin Gene Expression in Wool Fibre Development
- Hair follicle-specific keratins and their diseases
- Keratin Gene Expression Differences in Wool Follicles and Sequence Diversity of High Glycine-Tyrosine Keratin-Associated Proteins (Kaps) in Magra Sheep of India
- Purification of Porcine Hair Keratin Subunits and Their Immobilization for Use as Cell Culture Substrates