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- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Polymorphism of Exon V of prolactin gene and its association with Cashmere traits in Changthangi Pashmina goats
- Modulation of Photoaging-Induced Cutaneous Elastin: Evaluation of Gene and Protein Expression of Markers Related to Elastogenesis Under Different Photoexposure Conditions
- 197 A novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Real-world safety of Tepotinib: Insights from the Food and Drug Administration Adverse Event Reporting System
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- Genome-based analysis of the genetic pattern of black sheep in Qira sheep
- A second <i>KRT</i>71 allele in curly coated dogs
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Long-read RNA sequencing reveals extensive transcript isoform changes in a patient with IFAP syndrome with a recurrent intronic MBTPS2 variant
- Structure of human type II 5 alpha-reductase gene.
- Few Simple Sequence Repeats in Human Hair
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Characterization of a 190-Kilobase Pair Domain of Human Type I Hair Keratin Genes
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Structure of human type II 5 alpha-reductase gene
- Detection of five substitution TPO mutations in Polycystic Ovary Syndrome (PCOS) and thyroid hormones disturbance patients
- Matrix Stiffness-driven FAK Splicing Tunes Cell Mechanosensing
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1
- A Case Report of Werner’s Syndrome With a Novel Mutation From India