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Research 421–450 of 1000+
- Understanding key symptoms, side effects, and impacts of HR+/HER2- advanced breast cancer: qualitative study findings
- Health-related quality of life with sacituzumab govitecan in HR+/HER2− metastatic breast cancer in the phase III TROPiCS-02 trial
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- The Comparative Safety of Epirubicin and Cyclophosphamide versus Docetaxel and Cyclophosphamide in Lymph Node-Negative, HR-Positive, HER2-Negative Breast Cancer (ELEGANT): A Randomized Trial
- Formulation of Chitosan-Coated Brigatinib Nanospanlastics: Optimization, Characterization, Stability Assessment and In-Vitro Cytotoxicity Activity against H-1975 Cell Lines
- Vitamin D receptor: molecular signaling and actions of nutritional ligands in disease prevention
- Vitamin D metabolism and function in the skin
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Vitamin D and the skin: Physiology and pathophysiology
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- The role of vitamin D receptor mutations in the development of alopecia
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Development and progression of alopecia in the vitamin D receptor null mouse
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Quantification of the Vitamin D Receptor−Coregulator Interaction
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Congenital hair loss disorders: Rare, but not too rare
- Morphological Approach to Hair Disorders
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Hairless Modulates Ligand-Dependent Activation of the Vitamin D Receptor-Retinoid X Receptor Heterodimer
- Anatomic location of primary melanoma: Survival differences and sun exposure
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm