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Research 30 of 774
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Filaggrin mutations as an archetype for understanding the pathophysiology of atopic dermatitis
- Skin diseases associated with atopic dermatitis
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Editors' Picks
- FOXN1 Is Critical for Onycholemmal Terminal Differentiation in Nude (Foxn1nu) Mice
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- 9. Immunology and Genetics
- The Genetics of Human Skin Disease
- The nude gene and the skin
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Support for dermatological research in Sub‐Saharan Africa: insights from African hair and skin research programs
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Histologic morphology and involucrin, filaggrin, and keratin expression in normal canine skin from dogs of different breeds and coat types
- Deimination in epidermal barrier and hair formation
- Semidominant Inheritance in Epidermolytic Ichthyosis
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Learning from nudity: lessons from the nude phenotype
- Human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model
- Effects of a complex mixture prepared from agrimonia, houttuynia, licorice, peony, and phellodendron on human skin cells