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Research 121–150 of 1000+
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- The phenology of dioecious Ficus spp. tree species and its importance for forest restoration projects
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- The Phenotype of Circulating Follicular-Helper T Cells in Patients with Rheumatoid Arthritis Defines CD200 as a Potential Therapeutic Target
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Induction of ornithine decarboxylase in specific subpopulations of murine epidermal cells following multiple exposures to 12-<i>O</i>-tetradecanoylphorbol-13-acetate, mezerein and ethyl phenylpropriolate
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Severe Hair Loss of the Scalp due to a Hair Dye Containing Para phenylenediamine
- Renbök Phenomenon and Contact Sensitization in a Patient With Alopecia Universalis
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Characterization of Recombinant Human Liver Thermolabile Phenol Sulfotransferase with Minoxidil as the Substrate
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Lucio Phenomenon: Sequelae of Neglected Leprosy
- 3D spheroid culture synchronizes heterogeneous MSCs into an immunomodulatory phenotype with enhanced anti-inflammatory effects
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- DNA phenotyping: current application in forensic science
- Renbök phenomenon in a patient with alopecia areata universalis and psoriasis
- Contact immunotherapy-induced Renbök phenomenon in a patient with alopecia areata and psoriasis vulgaris
- Lichen planopilaris with Koebner phenomenon
- Chemical Leukoderma from Hair Dye Containing para-Phenylenediamine
- Pathobiology of the hairless phenotype: Dysregulation of hair follicle apoptosis and topobiology during the initiation of follicle cycling
- Implication of microRNA regulation in para-phenylenediamine-induced cell death and senescence in normal human hair dermal papilla cells
- Renbök Phenomenon in a Patient With Alopecia Areata Universalis
- The value of the free androgen index depends on the phenotype of polycystic ovary syndrome — a single-centre experience
- Lichen planopilaris caused by wig attachment: A Case of Koebner phenomenon in Frontal Fibrosing Alopecia
- KERATIN PHENOTYPES IN BASAL-CELL CARCINOMAS OF THE SKIN