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Research 241–270 of 1000+
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Woolly Antics between the Sheaths
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- The Genetics of Human Skin Disease
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- The nude gene and the skin
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Biochemistry of epidermal stem cells
- DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control epithelial differentiation
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Two females with hair loss
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Gene expression profile of human follicle dermal papilla cells in response to <i>Camellia japonica</i> phytoplacenta extract
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- The epidermis: rising to the surface
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Dynamics of Hair Follicle Morphogenesis and Skin Homeostasis
- Keratins and skin disease
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- New developments in the molecular treatment of ichthyosis: review of the literature