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Research 91–120 of 235
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- RNA interference of NtNCED3 reduces drought tolerance and impairs plant growth through feedback regulation of isoprenoids in Nicotiana tabacum
- Keratins of the Human Hair Follicle
- The organization of the keratin I and II gene clusters in placental mammals and marsupials show a striking similarity
- A functional role of S100A4/non-muscle myosin IIA axis for pro-tumorigenic vascular functions in glioblastoma
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Studies on the Proteome of Human Hair - Identification of Histones and Deamidated Keratins
- Application of PCR Technique to Detect Polymorphism of the KRTAP1.1 Gene in Three Sheep Breeds - A Review
- Variation in the ovine trichohyalin gene and its association with wool curvature
- Heat treatment increases the incidence of alopecia areata in the C3H/HeJ mouse model
- Skin precancer.
- Pruritic Trichostasis Spinulosa: A Rare Variant
- Type II Keratins Are Phosphorylated on a Unique Motif during Stress and Mitosis in Tissues and Cultured Cells
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Differential gene expression profiles in foetal skin of Rex rabbits with different wool density
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co-option in the evolution of the hair follicle
- Serum paroxonase 1 level may be an indicator and predictor of the severity of androgenetic alopecia
- Nitrate‐inducible NIGT1 proteins modulate phosphate uptake and starvation signalling via transcriptional regulation of <i>SPX</i> genes
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Clinical Management of Prostate Cancer in High-Risk Genetic Mutation Carriers
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Glycol Ethers and Neurodevelopment: Investigating the Impact of Prenatal Exposures
- Exercise in the management of polycystic ovary syndrome: A position statement from Exercise and Sports Science Australia
- Chemistry42: An AI-Driven Platform for Molecular Design and Optimization
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility