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Research 661–690 of 1000+
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- THE PATHOGENESIS OF ALOPECIA AREATA
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Molecular genetics of androgen insensitivity
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Induced pluripotent stem cell line MUSIi006-A derived from hair follicle keratinocytes as a non-invasive somatic cell source
- Genetic and hormonal influence on SARS-CoV-2-infection susceptibility
- The Roles of EDA2R in Ageing and Disease
- Pinkie, the First Viable Germline Hypomorph Allele of Retinoid X Receptor Alpha, Reveals an Important Role for RXRa in Th2 Development.
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Tabby pattern genetics – a whole new breed of cat
- The <i>IRE</i> gene encodes a protein kinase homologue and modulates root hair growth in <i>Arabidopsis</i>
- Unravelling the molecular basis for symbiotic signal transduction in legumes
- Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes
- The Molecular Biology of the Vitamin D Receptor
- Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon
- Ichthyosis