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Research 61–90 of 1000+
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- 604 DNA dioxygenases TET regulate keratin gene expression and enhancer networks within lineage-specific gene loci during epidermal and hair follicle-specific keratinocyte differentiation
- Multiomics Analysis of the Response to Ritlecitinib in Alopecia Areata Subtypes and Correlation With Efficacy
- Construction and Verification of Recombinant Follicle-specific Expression Vector
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Hair follicle-specific keratins and their diseases
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- The Overexpression of Tβ4 in the Hair Follicle Tissue of Alpas Cashmere Goats Increases Cashmere Yield and Promotes Hair Follicle Development
- Annotation of sheep keratin intermediate filament genes and their patterns of expression
- Keratin 17 Impacts Global Gene Expression and Controls G2/M Cell Cycle Transition in Ionizing Radiation–Induced Skin Damage
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Deletion of the <i>Sox21</i> gene drastically affects hair lipids
- Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11*1
- Identification and characterization of genes for skin and hair disorders
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Proteopedia entry: Coiled‐coil structure of keratins
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology
- Dissecting the Heterogeneity of Skin Gene Expression Patterns in Systemic Sclerosis
- Genes for intermediate filament proteins and the draft sequence of the human genome
- A new look into an old problem: keratins as tools to investigate determination, morphogenesis, and differentiation in skin.
- LB1034 Meta-analysis of scalp transcriptome defines alopecia areata subtypes and molecular response to four (4) treatments with jak inhibiting properties
- Congenital atrichia with papular lesions
- KRT16 wt Allele
- The human keratins: biology and pathology