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Research 301–330 of 1000+
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Successful Management of Netherton Syndrome Using IVIG and Dupilumab: A Case Report
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Clinical Snippets
- ‘Hard’ and ‘soft’ principles defining the structure, function and regulation of keratin intermediate filaments
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- The nude gene and the skin
- The Genetics of Human Skin Disease
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
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- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- New developments in the molecular treatment of ichthyosis: review of the literature
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Types I and II Keratin Intermediate Filaments
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Promotion of homology-directed DNA repair by polyamines
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization