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Research 31–60 of 1000+
- The Catalog of Human Hair Keratins
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient
- Seasonal Variability in Transcript Expression of Type I and Type II Keratins in Wool Follicles of Lustrous Fleece-Producing Magra Sheep
- Against the Rules: Human Keratin K80
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- Proteopedia entry: Coiled‐coil structure of keratins
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (<i>Atelerix albiventris</i>)
- Genome-wide identification, characterization, and expression analysis of keratin genes (KRTs) family in yak (Bos grunniens)
- A Group of Type I Keratin Genes on Human Chromosome 17: Characterization and Expression
- Expression analysis of the type I keratin protein keratin 33A in goat coat hair
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Hair follicle differentiation: expression, structure and evolutionary conservation of the hair type II keratin intermediate filament gene family
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Multiomics Analysis of the Response to Ritlecitinib in Alopecia Areata Subtypes and Correlation With Efficacy
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- Keratin 17 in disease pathogenesis: from cancer to dermatoses
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- 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
- Genomic Characterization of the Human Type I Cuticular Hair Keratin hHa2 and Identification of an Adjacent Novel Type I Hair Keratin Gene hHa5
- The Region Coding for the Helix Termination Motif and the Adjacent Intron 6 of the Human Type I Hair Keratin Gene hHa2 Contains Three Natural, Closely Spaced Polymorphic Sites
- Understanding the Nano‐topography Changes and Cellular Influences Resulting from the Surface Adsorption of Human Hair Keratins
- Bioinformatics analysis of genes associated with the patchy-type alopecia areata: CD2 may be a new therapeutic target
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity