Search
for
Sort by
Research 931–960 of 1000+
- 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
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Modulation of Vitamin D Receptor Activity by the Corepressor Hairless: Differential Effects of Hairless Isoforms
- Genetics of Structural Hair Disorders
- Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- Cheating on forensic hair testing? Detection of potential biomarkers for cosmetically altered hair samples using untargeted hair metabolomics
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Molecular Genetics of Alopecias
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Alopecia: Association with Resistance to Thyroid Hormones
- The Mammalian Hairless Protein as a DNA Binding Phosphoprotein
- Commentary on: Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- Werewolf, there wolf: variants in <i>Hairless</i> associated with hypotrichia and roaning in the lykoi cat breed
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Terapia por el arte
- The Reduction of Male Lower Urinary Tract Symptoms Is Associated With a Decreased Risk of Death
- Safety and quality of life of CDK4/6 inhibitors therapy for hormone receptor-positive, human epidermal growth factor receptor 2-negative advanced breast cancer: a multicenter cross-sectional survey in China
- The accelerated aging skin in rhino‐like SHJH<sup><i>hr</i></sup> mice