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Research 31–60 of 755
- The genetic basis of dermatophytosis skin infection susceptibility
- What does acne genetics teach us about disease pathogenesis?
- Newborn infant skin gene expression: Remarkable differences versus adults
- Dermatología en la Práctica Médica General Vol. 13
- An Intrinsic Oscillation of Gene Networks Inside Hair Follicle Stem Cells: An Additional Layer That Can Modulate Hair Stem Cell Activities
- Proprietary Herbal Extract Downregulates the Gene Expression of Il-1 and #945; in HaCaT Cells: Possible Implications Against Nonscarring Alopecia
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Effects of non-ablative fractional erbium glass laser treatment on gene regulation in human three-dimensional skin models
- Biochemical examination of fetal skin biopsy specimens obtained by fetoscopy: Use of the method for analysis of keratins and filaggrin
- Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis
- Concerted gene duplications in the two keratin gene families
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Trichohyalin: Presence in the Granular Layer and Stratum Corneum of Normal Human Epidermis
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- LB1077 Cutaneous responses to systemic iron: A potential role for epidermal turnover in mammalian iron excretion
- LB1081 Three-dimensional imaging of tight junction-network across multiple layers of human epidermis by array tomography using backscattered electron-mode scanning electron microscopy
- Genome-wide association study of skin complex diseases
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Learning from nudity: lessons from the nude phenotype
- Beyond Expectations
- The nude gene and the skin
- Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation