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Research 61–90 of 1000+
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- A homozygous single T deletion found in the GGCX gene with PXE-like phenotypes
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Hairless protein of Jumonji family and hair loss
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Hairless Modulates Ligand-Dependent Activation of the Vitamin D Receptor-Retinoid X Receptor Heterodimer
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Biology and Genetics of Hair
- Morphological Approach to Hair Disorders
- Hairless is a nuclear receptor corepressor essential for skin function
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- Commentary on: Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Hairless: A nuclear receptor corepressor essential for skin function
- Modulation of Vitamin D Receptor Activity by the Corepressor Hairless: Differential Effects of Hairless Isoforms
- A Newborn With Hair Loss
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Netherton Syndrome: A Case-Based Review of Diagnosis, Management, and Emerging Treatments.
- Bendamustine: an Old Drug in the New Era for Patients with Non-Hodgkin Lymphomas and Chronic Lymphocytic Leukemia
- Outcomes in Clinically Relevant Patient Subgroups From the EMBRACA Study: Talazoparib vs Physician’s Choice Standard-of-Care Chemotherapy
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Analysis of hairless corepressor mutants to characterize molecular cooperation with the vitamin D receptor in promoting the mammalian hair cycle
- Le gène<i>hairless</i>de la souris
- Congenital atrichia with papular lesions
- Gender determination in sport
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes