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Research 61–90 of 1000+
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- A curated catalog of canine and equine keratin genes
- Characterization of Novel Cutaneous Human Papillomavirus Genotypes HPV-150 and HPV-151
- Role of the Wnt signaling pathway in keratoacanthoma
- Oestrogen functions in skin and skin appendages
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Evolutionary Divergence of Fibroblast Growth Factors Across Species: Insight into Functional Diversification
- Genetic Defects of Female Sexual Differentiation
- Alopecia areata
- Hair follicle differentiation and regulation.
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Morpho-Regulation of Ectodermal Organs
- Extraskeletal actions of vitamin D
- MIM and Cortactin Antagonism Regulates Ciliogenesis and Hedgehog Signaling
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Generation and characterization of rat liver stem cell lines and their engraftment in a rat model of liver failure
- Repairing the lungs one breath at a time: How dedicated or facultative are you?
- Redefining hormone resistance in prostate cancer
- Roles of steroid sulfatase in brain and other tissues
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Genetics of Structural Hair Disorders
- Influence of Genotype and Hyperandrogenism on Sexual Function in Women With Congenital Adrenal Hyperplasia
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- The E6/E7 oncogenes of human papilloma virus and estradiol regulate hedgehog signaling activity in a murine model of cervical cancer