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Research 121–150 of 767
- Specific inhibition of FGF5-induced cell proliferation by RNA aptamers
- Structure and expression of the ovine Hoxc-13 gene
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- The Mask Mutation Identifies TMPRSS6 as an Essential Suppressor of Hepcidin Gene Expression, Required for Normal Uptake of Dietary Iron.
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- A syndromic extreme insulin resistance caused by biallelic POC1A mutations in exon 10
- Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- Hair keratin molecular dynamics models
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Male pattern hair loss: Taking one for the team: The selfless gene
- Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Clinical Snippets
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- Epidermal β-catenin activation remodels the dermis via paracrine signalling to distinct fibroblast lineages
- The activin binding proteins follistatin and follistatin-related protein are differentially regulated in vitro and during cutaneous wound repair
- Structures of three polycystic kidney disease-like domains from<i>Clostridium histolyticum</i>collagenases ColG and ColH
- Follicular Cell Implantation: An Emerging Cell Therapy for Hair Loss
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Chapter 23. Therapeutic Control of Androgen Action
- Normal head-hair length is correlated with its diameter
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Why Do Not All Chemotherapy Patients Lose Their Hair? Answering an Intriguing Question
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Oral Presentations
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells