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Research 331–360 of 1000+
- Hair follicle transcriptome profiles during the transition from anagen to catagen in Cashmere goat (Capra hircus)
- Wound healing mechanism in Mongolian gerbil skin
- Congenital atrichia with papular lesions
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- 175 Understanding immune privilege in an inducible mouse model of primary cicatrcial alopecia
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Research Snippets
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Hair greying is associated with active hair growth
- Identification of Key Genes and Signaling Pathways in Male Androgenetic Alopecia by Bioinformatics Analysis
- Coenzyme Q10 has anti-aging effects on human hair
- Human Hair Keratin‐Associated Proteins (KAPs)
- Hair keratin KRT81 is expressed in normal and breast cancer cells and contributes to their invasiveness
- The Overexpression of Tβ4 in the Hair Follicle Tissue of Alpas Cashmere Goats Increases Cashmere Yield and Promotes Hair Follicle Development
- Quantitative Analysis of Hair Luster in a Novel Ultraviolet-Irradiated Mouse Model
- Differential Gene Expression Screening Between Black and Gray Hairs Using Subtractive Library and DNA Chip
- The mouse keratin 6 isoforms are differentially expressed in the hair follicle, footpad, tongue and activated epidermis
- Identification of Telogen Markers Underscores that Telogen Is Far from a Quiescent Hair Cycle Phase
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Hair follicle-specific keratins and their diseases
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Characterization of the Human Hair Shaft Cuticle–Specific Keratin-Associated Protein 10 Family
- Upregulation of the truncated basic hair keratin 1(hHb1‐ΔN) in carcinoma cells by Epstein‐Barr virus (EBV)
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- ALOPECIA AREATA PROFILING SHOWS LNCRNAS REGULATE THE SUPPRESSED EXPRESSION OF KERATIN.