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Research 30 of 1000+
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers
- Diagnostic Value of VDR in Bone Metastasis and Prognosis of Patients with Breast Cancer and Expression Correlation between Vitamin D Receptor and Hairless Protein
- The Mammalian Hairless Protein as a DNA Binding Phosphoprotein
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Hairless protein of Jumonji family and hair loss
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Hairless is a nuclear receptor corepressor essential for skin function
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Commentary on: Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Hairless: A nuclear receptor corepressor essential for skin function
- The role of vitamin D receptor mutations in the development of alopecia
- Genetics of Structural Hair Disorders
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm