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Research 151–180 of 1000+
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- An immune regulatory CCT repeat containing oligodeoxynucleotide capable of causing hair loss in male mice
- Cutaneous Lymphadenoma Is a Distinct Trichoblastoma-like Lymphoepithelial Tumor With Diffuse Androgen Receptor Immunoreactivity, Notch1 Ligand in Reed-Sternberg–like Cells, and Common EGFR Somatic Mutations
- Australasian Society for Dermatology Research Meeting, May 2006
- Melanocytes: The new Black
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Identification of the cell lineage at the origin of basal cell carcinoma
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Towards Defining the Pathogenesis of the Hairless Phenotype
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Reversible Activation of c-Myc in Skin
- miR-150 regulates endothelial progenitor cell differentiation via Akt and promotes thrombus resolution
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Upregulation of interfollicular epidermal and hair infundibulum β-catenin expression in Gsdma3 mutant mice
- A newborn presenting with congenital blistering
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks