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Research 601–630 of 1000+
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Sequence, expression, and evolutionary conservation of a gene encoding a glycine/tyrosine-rich keratin-associated protein of hair.
- Structure of human type II 5 alpha-reductase gene
- Real-time iTRAQ-based proteome profiling revealed the central metabolism involved in nitrogen starvation induced lipid accumulation in microalgae
- Characterizing Wool Keratin
- Semecarpus anacardium Linn.: A review
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Long-Term Differential Changes in Mouse Intestinal Metabolomics after γ and Heavy Ion Radiation Exposure
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- The Enzymic Derivation of Citrulline Residues from Arginine Residues In Situ during the Biosynthesis of Hair Proteins that are Cross-Linked by Isopeptide Bonds
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- Identification of a preferred substrate peptide for transglutaminase 3 and detection of <i>in situ</i> activity in skin and hair follicles
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- Characteristic features of ageing in Korean women’s hair and scalp
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Serine-rich ultra high sulfur protein gene expression in murine hair and skin during the hair cycle.
- Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1
- UV damage of the hair.
- Pmg-1 and Pmg-2 constitute a novel family of KAP genes differentially expressed during skin and mammary gland development
- A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Protein deficiency in a colony of western lowland gorillas (Gorilla g. gorilla)
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Characterization of <i>BMP</i>2 gene expression in embryonic and adult Inner Mongolia Cashmere goat (<i>Capra hircus</i>) hair follicles
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- ADM Scaffolds Generate a Pro-regenerative Microenvironment During Full-Thickness Cutaneous Wound Healing Through M2 Macrophage Polarization via Lamtor1
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Identification of the C-terminal tail domain of AHF/trichohyalin as the critical site for modulation of the keratin filamentous meshwork in the keratinocyte
- Metabolic and transcriptomic reprogramming during contact inhibition-induced quiescence is mediated by YAP-dependent and YAP-independent mechanisms