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Research 31–60 of 1000+
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- Increased rate of hair keratin gene loss in the cetacean lineage
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Keratin Gene Expression in Wool Fibre Development
- Trichofolliculoma in a Family – An Unusual Occurrence
- Pmg-1 and Pmg-2 constitute a novel family of KAP genes differentially expressed during skin and mammary gland development
- Masquerading of trichotillomania in a family with monilethrix
- Discreet monilethrix: De novo mutation on the example of polish families
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Structure and expression of genes for a class of cysteine-rich proteins of the cuticle layers of differentiating wool and hair follicles.
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (<i>Atelerix albiventris</i>)
- <i>Hoxc13</i> and the development of hair follicle
- Multiomics Analysis of the Response to Ritlecitinib in Alopecia Areata Subtypes and Correlation With Efficacy
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11*1
- Cylindroma as Tumor of Hair Follicle Origin
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Study on the distribution of hair keratin in normal hair follicles by immunohistochemical staining
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Electrophoretic analysis of human hair keratins
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Diversity of Trichocyte Keratins and Keratin Associated Proteins
- ALOPECIA AREATA PROFILING SHOWS LNCRNAS REGULATE THE SUPPRESSED EXPRESSION OF KERATIN.