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Research 331–360 of 1000+
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Keratin disorders: from gene to therapy
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Regulation of masculinization: androgen signalling for external genitalia development
- FOXN1 deficient nude severe combined immunodeficiency
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- The molecular pathogenesis of Trichilemmal carcinoma
- Keratins: the hair shaft's backbone revealed
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Childhood Alopecia Areata: An Overview of Treatment and Recent Patents
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- Data from Synergistic Function of Smad4 and PTEN in Suppressing Forestomach Squamous Cell Carcinoma in the Mouse
- Data from Synergistic Function of Smad4 and PTEN in Suppressing Forestomach Squamous Cell Carcinoma in the Mouse
- Etiopathogenesis of acne
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Regulatory pathways implicated in male androgenetic alopecia pathogenesis